Crystallography Open Database

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Searching year of publication is 2015

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1520026 CIFC69.6 H77.2 B Cl5.2 N2 P Pt SP -113.4975; 13.6666; 19.036
93.409; 105.034; 95.788
3360.6Cowie, Bradley E.; Emslie, David J. H.
Bis-hydrocarbyl Platinum(II) Ambiphilic Ligand Complexes: Alkyl‒Aryl Exchange between Platinum and Boron
Organometallics, 2015, 34, 2737
1520027 CIFC27 H30 Ir1.04 N3 O3P 1 21/n 18.7533; 19.4098; 13.9131
90; 90.472; 90
2363.75Ruddlesden, Amy J.; Mewis, Ryan E.; Green, Gary G. R.; Whitwood, Adrian C.; Duckett, Simon B.
Catalytic Transfer of Magnetism Using a Neutral Iridium Phenoxide Complex
Organometallics, 2015, 34, 2997
1520028 CIFC7 H6 Br N OP 1 21/c 116.189; 4.6448; 9.8821
90; 92.866; 90
742.15Gulyás, Henrik; Rivilla, Ivan; Curreli, Simona; Freixa, Zoraida; van Leeuwen, Piet W. N. M.
Highly active, chemo- and enantioselective Pt-SPO catalytic systems for the synthesis of aromatic carboxamides
Catal. Sci. Technol., 2015, 5, 3822
1520029 CIFC7 H6 Br N OP 1 21/n 15.0263; 10.9683; 13.3113
90; 93.465; 90
732.51Gulyás, Henrik; Rivilla, Ivan; Curreli, Simona; Freixa, Zoraida; van Leeuwen, Piet W. N. M.
Highly active, chemo- and enantioselective Pt-SPO catalytic systems for the synthesis of aromatic carboxamides
Catal. Sci. Technol., 2015, 5, 3822
1520030 CIFC22 H16 N2 O2P 1 21/n 19.3024; 8.3301; 21.227
90; 94.1; 90
1640.7Gulyás, Henrik; Rivilla, Ivan; Curreli, Simona; Freixa, Zoraida; van Leeuwen, Piet W. N. M.
Highly active, chemo- and enantioselective Pt-SPO catalytic systems for the synthesis of aromatic carboxamides
Catal. Sci. Technol., 2015, 5, 3822
1520031 CIFC22 H12 N2P 1 21/c 112.3869; 7.756; 16.0899
90; 95.514; 90
1538.65Gulyás, Henrik; Rivilla, Ivan; Curreli, Simona; Freixa, Zoraida; van Leeuwen, Piet W. N. M.
Highly active, chemo- and enantioselective Pt-SPO catalytic systems for the synthesis of aromatic carboxamides
Catal. Sci. Technol., 2015, 5, 3822
1520032 CIFC22 H12 N2P 1 21 17.874; 7.9775; 12.3173
90; 92.715; 90
772.84Gulyás, Henrik; Rivilla, Ivan; Curreli, Simona; Freixa, Zoraida; van Leeuwen, Piet W. N. M.
Highly active, chemo- and enantioselective Pt-SPO catalytic systems for the synthesis of aromatic carboxamides
Catal. Sci. Technol., 2015, 5, 3822
1520033 CIFC28 H23 O PP 21 21 217.9622; 12.3209; 21.0198
90; 90; 90
2062.07Gulyás, Henrik; Rivilla, Ivan; Curreli, Simona; Freixa, Zoraida; van Leeuwen, Piet W. N. M.
Highly active, chemo- and enantioselective Pt-SPO catalytic systems for the synthesis of aromatic carboxamides
Catal. Sci. Technol., 2015, 5, 3822
1520034 CIFC7 H6 Br N OP 1 21/c 14.92; 5.3316; 27.538
90; 93.562; 90
721Gulyás, Henrik; Rivilla, Ivan; Curreli, Simona; Freixa, Zoraida; van Leeuwen, Piet W. N. M.
Highly active, chemo- and enantioselective Pt-SPO catalytic systems for the synthesis of aromatic carboxamides
Catal. Sci. Technol., 2015, 5, 3822
1520035 CIFC38 H34 Cl6 Cr Fe Mn N6 O14C 1 2/c 114.2177; 22.9278; 14.5428
90; 105.118; 90
4576.6Abhervé, Alexandre; Mañas-Valero, Samuel; Clemente-León, Miguel; Coronado, Eugenio
Graphene related magnetic materials: micromechanical exfoliation of 2D layered magnets based on bimetallic anilate complexes with inserted [FeIII(acac2-trien)]+and [FeIII(sal2-trien)]+molecules
Chem. Sci., 2015, 6, 4665
1520036 CIFC38 H34 Br6 Cr Fe Mn N6 O14C 1 2/c 114.1914; 23.0061; 14.788
90; 104.703; 90
4670Abhervé, Alexandre; Mañas-Valero, Samuel; Clemente-León, Miguel; Coronado, Eugenio
Graphene related magnetic materials: micromechanical exfoliation of 2D layered magnets based on bimetallic anilate complexes with inserted [FeIII(acac2-trien)]+and [FeIII(sal2-trien)]+molecules
Chem. Sci., 2015, 6, 4665
1520037 CIFC38 H34 Br6 Cr Ga Mn N6 O14C 1 2/c 114.1613; 23.0839; 14.8676
90; 104.296; 90
4709.7Abhervé, Alexandre; Mañas-Valero, Samuel; Clemente-León, Miguel; Coronado, Eugenio
Graphene related magnetic materials: micromechanical exfoliation of 2D layered magnets based on bimetallic anilate complexes with inserted [FeIII(acac2-trien)]+and [FeIII(sal2-trien)]+molecules
Chem. Sci., 2015, 6, 4665
1520038 CIFC26 H24 N2 O4P 1 21/c 19.7172; 11.762; 19.84
90; 99.84; 90
2234.2Zhu, Qiuhua; Zhang, Yilin; Nie, Han; Zhao, Zujin; Liu, Shuwen; Wong, Kam Sing; Tang, Ben Zhong
Insight into the strong aggregation-induced emission of low-conjugated racemic C6-unsubstituted tetrahydropyrimidines through crystal-structure‒property relationship of polymorphs
Chem. Sci., 2015, 6, 4690
1520039 CIFC26 H24 N2 O4P 1 21/n 19.591; 14.916; 15.744
90; 91.79; 90
2251.2Zhu, Qiuhua; Zhang, Yilin; Nie, Han; Zhao, Zujin; Liu, Shuwen; Wong, Kam Sing; Tang, Ben Zhong
Insight into the strong aggregation-induced emission of low-conjugated racemic C6-unsubstituted tetrahydropyrimidines through crystal-structure‒property relationship of polymorphs
Chem. Sci., 2015, 6, 4690
1520040 CIFC26 H22 Br2 N2 O4P -110.6774; 10.7451; 12.3472
107.453; 103.856; 103.585
1238.02Zhu, Qiuhua; Zhang, Yilin; Nie, Han; Zhao, Zujin; Liu, Shuwen; Wong, Kam Sing; Tang, Ben Zhong
Insight into the strong aggregation-induced emission of low-conjugated racemic C6-unsubstituted tetrahydropyrimidines through crystal-structure‒property relationship of polymorphs
Chem. Sci., 2015, 6, 4690
1520041 CIFC26 H22 Br2 N2 O4P -112.571; 13.241; 15.845
87.14; 76.74; 74.96
2479.1Zhu, Qiuhua; Zhang, Yilin; Nie, Han; Zhao, Zujin; Liu, Shuwen; Wong, Kam Sing; Tang, Ben Zhong
Insight into the strong aggregation-induced emission of low-conjugated racemic C6-unsubstituted tetrahydropyrimidines through crystal-structure‒property relationship of polymorphs
Chem. Sci., 2015, 6, 4690
1520042 CIFC26 H22 Br2 N2 O4P b c a11.755; 20.78; 21.031
90; 90; 90
5137Zhu, Qiuhua; Zhang, Yilin; Nie, Han; Zhao, Zujin; Liu, Shuwen; Wong, Kam Sing; Tang, Ben Zhong
Insight into the strong aggregation-induced emission of low-conjugated racemic C6-unsubstituted tetrahydropyrimidines through crystal-structure‒property relationship of polymorphs
Chem. Sci., 2015, 6, 4690
1520043 CIFC28 H22 Br2 N6 O2P 1 21/c 113.5422; 19.675; 10.2805
90; 100.796; 90
2690.7Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520044 CIFC28 H22 Br2 N6 O2P 1 21/c 114.5095; 20.268; 9.5541
90; 97.192; 90
2787.6Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520045 CIFC28 H22 Cl2 N6 O2P 1 21/c 115.6181; 15.7722; 10.6301
90; 95.137; 90
2608Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520046 CIFC28 H22 Cl2 N6 O2P 1 21/c 115.6347; 15.989; 10.646
90; 95.252; 90
2650.1Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520047 CIFC28 H22 Cl2 N6 O2P 1 21/c 114.4187; 19.4064; 9.7692
90; 95.552; 90
2720.7Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520048 CIFC28 H22 Cl2 N6 O2P 1 21/c 114.4; 19.51; 9.757
90; 95.784; 90
2727.2Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520049 CIFC28 H22 I2 N6 O2P -18.982; 12.5271; 26.146
84.5; 89.331; 74.563
2822.4Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520050 CIFC28 H22 I2 N6 O2P -19.048; 12.5933; 26.305
83.815; 89.271; 75.005
2878Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520051 CIFC11 H9 N3P 21 21 215.9077; 7.4479; 21.752
90; 90; 90
957.1Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520052 CIFC11 H9 N3P 21 21 215.911; 7.496; 21.82
90; 90; 90
967Hutchins, Kristin M.; Groeneman, Ryan H.; Reinheimer, Eric W.; Swenson, Dale C.; MacGillivray, Leonard R.
Achieving dynamic behaviour and thermal expansion in the organic solid state via co-crystallization
Chem. Sci., 2015, 6, 4717
1520053 CIFC6 H24 I8 N2 O2 Pb3 S2C m c 214.6212; 27.484; 26.923
90; 90; 90
3419.5Rong, Yaoguang; Tang, Zhongjia; Zhao, Yufeng; Zhong, Xin; Venkatesan, Swaminathan; Graham, Harrison; Patton, Matthew; Jing, Yan; Guloy, Arnold M.; Yao, Yan
Solvent engineering towards controlled grain growth in perovskite planar heterojunction solar cells.
Nanoscale, 2015, 7, 10595-10599
1520054 CIFC26 H33 Cl4 N5 Nb2P 1 21/c 115.913; 13.362; 15.947
90; 95.548; 90
3374.9Saito, Teruhiko; Nishiyama, Haruka; Kawakita, Kento; Nechayev, Michael; Kriegel, Benjamin; Tsurugi, Hayato; Arnold, John; Mashima, Kazushi
Reduction of ((t)BuN═)NbCl3(py)2 in a Salt-Free Manner for Generating Nb(IV) Dinuclear Complexes and Their Reactivity toward Benzo[c]cinnoline.
Inorganic chemistry, 2015, 54, 6004-6009
1520055 CIFC23 H33 Cl4 N5 Nb2P -18.5962; 11.0422; 15.754
87.369; 83.921; 77.279
1450.1Saito, Teruhiko; Nishiyama, Haruka; Kawakita, Kento; Nechayev, Michael; Kriegel, Benjamin; Tsurugi, Hayato; Arnold, John; Mashima, Kazushi
Reduction of ((t)BuN═)NbCl3(py)2 in a Salt-Free Manner for Generating Nb(IV) Dinuclear Complexes and Their Reactivity toward Benzo[c]cinnoline.
Inorganic chemistry, 2015, 54, 6004-6009
1520056 CIFC31.5 H48 Cl4 N6 Nb2 O2P -18.4679; 15.5173; 15.6028
90.009; 92.687; 92.922
2045.3Saito, Teruhiko; Nishiyama, Haruka; Kawakita, Kento; Nechayev, Michael; Kriegel, Benjamin; Tsurugi, Hayato; Arnold, John; Mashima, Kazushi
Reduction of ((t)BuN═)NbCl3(py)2 in a Salt-Free Manner for Generating Nb(IV) Dinuclear Complexes and Their Reactivity toward Benzo[c]cinnoline.
Inorganic chemistry, 2015, 54, 6004-6009
1520057 CIFC53 H54 Cl4 N7 Nb2P -19.8238; 14.484; 18.6974
95.12; 93.115; 92.248
2643.3Saito, Teruhiko; Nishiyama, Haruka; Kawakita, Kento; Nechayev, Michael; Kriegel, Benjamin; Tsurugi, Hayato; Arnold, John; Mashima, Kazushi
Reduction of ((t)BuN═)NbCl3(py)2 in a Salt-Free Manner for Generating Nb(IV) Dinuclear Complexes and Their Reactivity toward Benzo[c]cinnoline.
Inorganic chemistry, 2015, 54, 6004-6009
1520058 CIFMo O9 Te2 ThC 1 2/c 121.431; 7.046; 10.923
90; 110.33; 90
1546.7Xiao, Bin; Klinkenberg, Martina; Bosbach, Dirk; Suleimanov, Evgeny V.; Alekseev, Evgeny V.
Effects of Te(IV) Oxo-Anion Incorporation into Thorium Molybdates and Tungstates.
Inorganic chemistry, 2015, 54, 5981-5990
1520059 CIFMo O13 Te3 Th2P 1 21/c 111.379; 7.1208; 14.06
90; 90.6; 90
1139.2Xiao, Bin; Klinkenberg, Martina; Bosbach, Dirk; Suleimanov, Evgeny V.; Alekseev, Evgeny V.
Effects of Te(IV) Oxo-Anion Incorporation into Thorium Molybdates and Tungstates.
Inorganic chemistry, 2015, 54, 5981-5990
1520060 CIFO9 Te2 Th WI 41/a :219.4824; 19.4824; 7.743
90; 90; 90
2939Xiao, Bin; Klinkenberg, Martina; Bosbach, Dirk; Suleimanov, Evgeny V.; Alekseev, Evgeny V.
Effects of Te(IV) Oxo-Anion Incorporation into Thorium Molybdates and Tungstates.
Inorganic chemistry, 2015, 54, 5981-5990
1520061 CIFO7 Te Th WP 1 21/c 14.1252; 8.5122; 15.364
90; 92.599; 90
538.94Xiao, Bin; Klinkenberg, Martina; Bosbach, Dirk; Suleimanov, Evgeny V.; Alekseev, Evgeny V.
Effects of Te(IV) Oxo-Anion Incorporation into Thorium Molybdates and Tungstates.
Inorganic chemistry, 2015, 54, 5981-5990
1520062 CIFC40 H23 F12 N14 O0.5 P2 RuP -19.2489; 12.1579; 18.0824
82.455; 82.843; 81.221
1980.72Cloonan, Suzanne M.; Elmes, Robert B. P.; Erby, MariaLuisa; Bright, Sandra A.; Poynton, Fergus E.; Nolan, Derek E.; Quinn, Susan J.; Gunnlaugsson, Thorfinnur; Williams, D. Clive
Detailed Biological Profiling of a Photoactivated and Apoptosis Inducing pdppz Ruthenium(II) Polypyridyl Complex in Cancer Cells.
Journal of medicinal chemistry, 2015, 58, 4494-4505
1520063 CIFC4 H2 N10 O6P 1 21/c 15.6265; 9.1195; 9.5532
90; 97.913; 90
485.52Zhang, Jiaheng; Shreeve, Jean’ne M.
Nitroaminofurazans with Azo and Azoxy Linkages: A Comparative Study of Structural, Electronic, Physicochemical, and Energetic Properties
The Journal of Physical Chemistry C, 2015, 119, 12887
1520064 CIFC4 H2 N10 O7P 1 n 17.8; 8.2; 8.6
90; 115.4; 90
496.9Zhang, Jiaheng; Shreeve, Jean’ne M.
Nitroaminofurazans with Azo and Azoxy Linkages: A Comparative Study of Structural, Electronic, Physicochemical, and Energetic Properties
The Journal of Physical Chemistry C, 2015, 119, 12887
1520065 CIFC29 H34 F3 Ir N2 O4P b c a20.8528; 11.8997; 22.661
90; 90; 90
5623.1Zhou, Meng; Johnson, Samantha I.; Gao, Yang; Emge, Thomas J.; Nielsen, Robert J.; Goddard, William A.; Goldman, Alan S.
Activation and Oxidation of Mesitylene C‒H Bonds by (Phebox)Iridium(III) Complexes
Organometallics, 2015, 34, 2879
1520066 CIFC29 H37 Ir N2 O4P b c a20.532; 11.9277; 22.489
90; 90; 90
5507.5Zhou, Meng; Johnson, Samantha I.; Gao, Yang; Emge, Thomas J.; Nielsen, Robert J.; Goddard, William A.; Goldman, Alan S.
Activation and Oxidation of Mesitylene C‒H Bonds by (Phebox)Iridium(III) Complexes
Organometallics, 2015, 34, 2879
1520067 CIFC22 H25 F6 Ir N2 O7P -19.1482; 10.3381; 14.352
97.296; 107.21; 99.526
1256.2Zhou, Meng; Johnson, Samantha I.; Gao, Yang; Emge, Thomas J.; Nielsen, Robert J.; Goddard, William A.; Goldman, Alan S.
Activation and Oxidation of Mesitylene C‒H Bonds by (Phebox)Iridium(III) Complexes
Organometallics, 2015, 34, 2879
1520068 CIFC32 H36 Br2 N4 O2P 1 21/c 110.037; 8.2451; 18.991
90; 101.279; 90
1541.3Zhu, Xiaxia; Du, Haifeng
A Highly Stereoselective Metal-Free Hydrogenation of Diimines for the Synthesis of Cis-Vicinal Diamines.
Organic letters, 2015, 17, 3106-3109
1520069 CIFC17 H39 Cl2 Fe N P2P 21 21 2110.9222; 11.7618; 17.7375
90; 90; 90
2278.64Zhang, Yuanyuan; MacIntosh, Alex D.; Wong, Janice L.; Bielinski, Elizabeth A.; Williard, Paul G.; Mercado, Brandon Q.; Hazari, Nilay; Bernskoetter, Wesley H.
Iron catalyzed CO2hydrogenation to formate enhanced by Lewis acid co-catalysts
Chem. Sci., 2015, 6, 4291
1520070 CIFC17 H44 B Fe N P2C 1 2/c 131.925; 7.968; 21.06
90; 121.335; 90
4575.8Zhang, Yuanyuan; MacIntosh, Alex D.; Wong, Janice L.; Bielinski, Elizabeth A.; Williard, Paul G.; Mercado, Brandon Q.; Hazari, Nilay; Bernskoetter, Wesley H.
Iron catalyzed CO2hydrogenation to formate enhanced by Lewis acid co-catalysts
Chem. Sci., 2015, 6, 4291
1520071 CIFC18 H44 B Fe N O P2P 1 21/n 18.4128; 31.269; 9.8709
90; 114.779; 90
2357.6Zhang, Yuanyuan; MacIntosh, Alex D.; Wong, Janice L.; Bielinski, Elizabeth A.; Williard, Paul G.; Mercado, Brandon Q.; Hazari, Nilay; Bernskoetter, Wesley H.
Iron catalyzed CO2hydrogenation to formate enhanced by Lewis acid co-catalysts
Chem. Sci., 2015, 6, 4291
1520072 CIFC18 H41 Fe N O P2P 1 21/n 18.0283; 12.8902; 21.842
90; 98.351; 90
2236.4Zhang, Yuanyuan; MacIntosh, Alex D.; Wong, Janice L.; Bielinski, Elizabeth A.; Williard, Paul G.; Mercado, Brandon Q.; Hazari, Nilay; Bernskoetter, Wesley H.
Iron catalyzed CO2hydrogenation to formate enhanced by Lewis acid co-catalysts
Chem. Sci., 2015, 6, 4291
1520073 CIFC18 H41 Fe N O P2P 1 21/n 111.5836; 15.4917; 13.1032
90; 110.887; 90
2196.85Zhang, Yuanyuan; MacIntosh, Alex D.; Wong, Janice L.; Bielinski, Elizabeth A.; Williard, Paul G.; Mercado, Brandon Q.; Hazari, Nilay; Bernskoetter, Wesley H.
Iron catalyzed CO2hydrogenation to formate enhanced by Lewis acid co-catalysts
Chem. Sci., 2015, 6, 4291
1520074 CIFC19 H41 Fe N O3 P2P 4111.736; 11.736; 16.678
90; 90; 90
2297.1Zhang, Yuanyuan; MacIntosh, Alex D.; Wong, Janice L.; Bielinski, Elizabeth A.; Williard, Paul G.; Mercado, Brandon Q.; Hazari, Nilay; Bernskoetter, Wesley H.
Iron catalyzed CO2hydrogenation to formate enhanced by Lewis acid co-catalysts
Chem. Sci., 2015, 6, 4291
1520075 CIFC23 H49 Fe N O3 P2P 1 21/n 115.4197; 12.0975; 16.0962
90; 114.498; 90
2732.3Zhang, Yuanyuan; MacIntosh, Alex D.; Wong, Janice L.; Bielinski, Elizabeth A.; Williard, Paul G.; Mercado, Brandon Q.; Hazari, Nilay; Bernskoetter, Wesley H.
Iron catalyzed CO2hydrogenation to formate enhanced by Lewis acid co-catalysts
Chem. Sci., 2015, 6, 4291
1520076 CIFC108 H108 Ag2 B20 P6P 1 21/c 112.828; 25.0953; 21.3666
90; 131.748; 90
5131.8Avdeeva, Varvara V.; Buzin, Mikhail I.; Malinina, Elena A.; Kuznetsov, Nikolay T.; Vologzhanina, Anna V.
Reversible single-crystal-to-single-crystal photoisomerization of a silver(i) macropolyhedral borane
CrystEngComm, 2015, 17, 8870
1520077 CIFC108 H108 Ag2 B20 P6P 1 21/c 112.9112; 25.0981; 21.0634
90; 131.739; 90
5093.1Avdeeva, Varvara V.; Buzin, Mikhail I.; Malinina, Elena A.; Kuznetsov, Nikolay T.; Vologzhanina, Anna V.
Reversible single-crystal-to-single-crystal photoisomerization of a silver(i) macropolyhedral borane
CrystEngComm, 2015, 17, 8870
1520078 CIFC108 H108 Ag2 B20 P6P 1 21/c 112.99; 25.155; 21.7332
90; 131.733; 90
5299.6Avdeeva, Varvara V.; Buzin, Mikhail I.; Malinina, Elena A.; Kuznetsov, Nikolay T.; Vologzhanina, Anna V.
Reversible single-crystal-to-single-crystal photoisomerization of a silver(i) macropolyhedral borane
CrystEngComm, 2015, 17, 8870
1520079 CIFC12 H0.25 O13 Zn3C 1 2/c 117.1017; 13.7034; 10.0254
90; 105.429; 90
2264.8Li, Huan-Huan; Niu, Zheng; Chen, Long; Jiang, Hao-Bin; Wang, Ya-Ping; Cheng, Peng
Three luminescent metal‒organic frameworks constructed from trinuclear zinc(ii) clusters and furan-2,5-dicarboxylate
CrystEngComm, 2015, 17, 5101
1520080 CIFC65 H69 N7 O44.17 Zn6P -112.6947; 12.8242; 14.7971
85.11; 65.988; 89.663
2191.4Li, Huan-Huan; Niu, Zheng; Chen, Long; Jiang, Hao-Bin; Wang, Ya-Ping; Cheng, Peng
Three luminescent metal‒organic frameworks constructed from trinuclear zinc(ii) clusters and furan-2,5-dicarboxylate
CrystEngComm, 2015, 17, 5101
1520081 CIFC17 H19 N2 O11 Zn1.5P 1 21/c 19.3468; 15.2267; 17.6517
90; 95.599; 90
2500.2Li, Huan-Huan; Niu, Zheng; Chen, Long; Jiang, Hao-Bin; Wang, Ya-Ping; Cheng, Peng
Three luminescent metal‒organic frameworks constructed from trinuclear zinc(ii) clusters and furan-2,5-dicarboxylate
CrystEngComm, 2015, 17, 5101
1520082 CIFC61.5 H86 Co2 Dy2 N8 O24P -114.068; 21.394; 26.2804
67.4228; 86.9557; 89.2403
7292.9Berkoff, Benjamin; Griffiths, Kieran; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Escuer, Albert; Kostakis, George E.
A new family of high nuclearity Co(II)/Dy(III) coordination clusters possessing robust and unseen topologies.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12788-12795
1520083 CIFC54 H74 Co Dy3 N9 O25C 1 2/c 117.0866; 19.9394; 20.2635
90; 109.693; 90
6499.9Berkoff, Benjamin; Griffiths, Kieran; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Escuer, Albert; Kostakis, George E.
A new family of high nuclearity Co(II)/Dy(III) coordination clusters possessing robust and unseen topologies.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12788-12795
1520084 CIFC310 H404 Co10 Dy13 N33 O105P -113.7063; 25.959; 32.551
73.03; 88.444; 89.026
11072.8Berkoff, Benjamin; Griffiths, Kieran; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Escuer, Albert; Kostakis, George E.
A new family of high nuclearity Co(II)/Dy(III) coordination clusters possessing robust and unseen topologies.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12788-12795
1520085 CIFC120 H154 Co4 Dy4 N14 O34P 6/m27.7587; 27.7587; 22.5433
90; 90; 120
15043.4Berkoff, Benjamin; Griffiths, Kieran; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Escuer, Albert; Kostakis, George E.
A new family of high nuclearity Co(II)/Dy(III) coordination clusters possessing robust and unseen topologies.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12788-12795
1520086 CIFC92 H129 Co2 Dy5 N10 O37P b c a28.3983; 17.1091; 23.8614
90; 90; 90
11593.5Berkoff, Benjamin; Griffiths, Kieran; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Escuer, Albert; Kostakis, George E.
A new family of high nuclearity Co(II)/Dy(III) coordination clusters possessing robust and unseen topologies.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12788-12795
1520087 CIFC52 H72 Co2 Dy2 N10 O28C 1 2/c 124.6279; 12.2953; 26.851
90; 115.817; 90
7319.2Berkoff, Benjamin; Griffiths, Kieran; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Escuer, Albert; Kostakis, George E.
A new family of high nuclearity Co(II)/Dy(III) coordination clusters possessing robust and unseen topologies.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12788-12795
1520088 CIFC150 H116 Co3 N28 O4 W2P 1 21/c 115.73; 29.011; 15.857
90; 110.416; 90
6782Zhao, Liang; Duan, Ran; Zhuang, Peng-Fei; Zheng, Hui; Jiao, Cheng-Qi; Wang, Jun-Li; He, Cheng; Liu, Tao
12-Metal 36-membered ring based W(V)-Co(II) layers showing spin-glass behavior.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12613-12617
1520089 CIFC172 H130 Co3 N28 O6 W2P -115.2452; 16.9866; 17.9387
111.222; 99.768; 104.345
4018.72Zhao, Liang; Duan, Ran; Zhuang, Peng-Fei; Zheng, Hui; Jiao, Cheng-Qi; Wang, Jun-Li; He, Cheng; Liu, Tao
12-Metal 36-membered ring based W(V)-Co(II) layers showing spin-glass behavior.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12613-12617
1520090 CIFC14 H14 N2 Ni O7P 1 21/c 16.585; 25.608; 8.656
90; 96.73; 90
1449.6Miklovič, Jozef; Valigura, Dušan; Boča, Roman; Titiš, Ján
A mononuclear Ni(ii) complex: a field induced single-molecule magnet showing two slow relaxation processes.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12484-12487
1520091 CIFC8 H106 As2 Fe4 La2 N2 O116 W18P -112.6669; 13.5788; 16.3488
107.303; 99.72; 96.736
2604Chen, Lijuan; Zhang, Fang; Ma, Xing; Luo, Jie; Zhao, Junwei
Two types of novel tetra-iron substituted sandwich-type arsenotungastates with supporting lanthanide pendants.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12598-12612
1520092 CIFC8 H106 As2 Fe4 N2 O116 Pr2 W18P -112.6523; 13.5456; 16.272
107.169; 99.786; 96.861
2582.7Chen, Lijuan; Zhang, Fang; Ma, Xing; Luo, Jie; Zhao, Junwei
Two types of novel tetra-iron substituted sandwich-type arsenotungastates with supporting lanthanide pendants.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12598-12612
1520093 CIFC8 H106 As2 Fe4 N2 Nd2 O116 W18P -112.6668; 13.5691; 16.3027
107.127; 99.763; 96.876
2595.8Chen, Lijuan; Zhang, Fang; Ma, Xing; Luo, Jie; Zhao, Junwei
Two types of novel tetra-iron substituted sandwich-type arsenotungastates with supporting lanthanide pendants.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12598-12612
1520094 CIFC8 H106 As2 Fe4 N2 O116 Sm2 W18P -112.6577; 13.5693; 16.278
107.165; 99.801; 96.896
2588.9Chen, Lijuan; Zhang, Fang; Ma, Xing; Luo, Jie; Zhao, Junwei
Two types of novel tetra-iron substituted sandwich-type arsenotungastates with supporting lanthanide pendants.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12598-12612
1520095 CIFC8 H106 As2 Eu2 Fe4 N2 O116 W18P -112.6292; 13.5134; 16.1999
106.993; 99.753; 97.011
2562.3Chen, Lijuan; Zhang, Fang; Ma, Xing; Luo, Jie; Zhao, Junwei
Two types of novel tetra-iron substituted sandwich-type arsenotungastates with supporting lanthanide pendants.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12598-12612
1520096 CIFC8 H106 As2 Fe4 Gd2 N2 O116 W18P -112.623; 13.5118; 16.1922
106.789; 99.755; 97.152
2561.4Chen, Lijuan; Zhang, Fang; Ma, Xing; Luo, Jie; Zhao, Junwei
Two types of novel tetra-iron substituted sandwich-type arsenotungastates with supporting lanthanide pendants.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12598-12612
1520097 CIFC8 H106 As2 Fe4 N2 O116 Tb2 W18P -112.6063; 13.4464; 16.0241
106.473; 99.828; 97.29
2522Chen, Lijuan; Zhang, Fang; Ma, Xing; Luo, Jie; Zhao, Junwei
Two types of novel tetra-iron substituted sandwich-type arsenotungastates with supporting lanthanide pendants.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12598-12612
1520098 CIFC8 H106 As2 Dy2 Fe4 N2 O116 W18P -112.6307; 13.5293; 16.195
106.853; 99.776; 97.153
2565.5Chen, Lijuan; Zhang, Fang; Ma, Xing; Luo, Jie; Zhao, Junwei
Two types of novel tetra-iron substituted sandwich-type arsenotungastates with supporting lanthanide pendants.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12598-12612
1520099 CIFC8 H106 As2 Er2 Fe4 N2 O116 W18P -112.5799; 13.4462; 16.0508
106.507; 99.813; 97.325
2520.2Chen, Lijuan; Zhang, Fang; Ma, Xing; Luo, Jie; Zhao, Junwei
Two types of novel tetra-iron substituted sandwich-type arsenotungastates with supporting lanthanide pendants.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12598-12612
1520100 CIFC62 H60 N18 O18 Zn3P -114.0738; 14.4682; 18.1303
82.254; 81.01; 68.154
3372.7Singh, Jasminder; Yadav, Manisha; Singh, Ajnesh; Singh, Narinder
Zinc metal complex as a sensor for simultaneous detection of fluoride and HSO4(-) ions.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12589-12597
1520101 CIFC34.08 H27.23 Cl Cu N4 O1.58P 1 21/c 110.0513; 28.1929; 12.2189
90; 112.243; 90
3204.88Hua, Carol; Turner, Peter; D'Alessandro, Deanna M
Facile redox state manipulation in Cu(i) frameworks by utilisation of the redox-active tris(4-(pyridin-4-yl)phenyl)amine ligand.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 15297-15303
1520102 CIFC33 H24 Cl Cu N4P 1 21/c 110.0513; 28.1929; 12.2189
90; 112.243; 90
3204.88Hua, Carol; Turner, Peter; D'Alessandro, Deanna M
Facile redox state manipulation in Cu(i) frameworks by utilisation of the redox-active tris(4-(pyridin-4-yl)phenyl)amine ligand.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 15297-15303
1520103 CIFC34.5 H24 Cu N5.5 O5.62P 2 2 219.077; 13.831; 32.773
90; 90; 90
4114.5Hua, Carol; Turner, Peter; D'Alessandro, Deanna M
Facile redox state manipulation in Cu(i) frameworks by utilisation of the redox-active tris(4-(pyridin-4-yl)phenyl)amine ligand.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 15297-15303
1520104 CIFC33 H24 Cu N5 O3P 2 2 219.077; 13.831; 32.773
90; 90; 90
4114.5Hua, Carol; Turner, Peter; D'Alessandro, Deanna M
Facile redox state manipulation in Cu(i) frameworks by utilisation of the redox-active tris(4-(pyridin-4-yl)phenyl)amine ligand.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 15297-15303
1520105 CIFC72 H80 N4 O18P -112.6007; 16.0006; 17.3353
106.074; 101.073; 92.406
3279.14Kelong Zhu; Christopher A. O'Keefe; V. Nicholas Vukotic; Robert W. Schurko; Stephen J. Loeb
A molecular shuttle that operates inside a metal-organic framework
Nature Chemistry, 2015, 7, 514-519
1520106 CIFC224 H273 B3 F12 N12 O66 Zn8R 3 2 :H33.03; 33.03; 28.099
90; 90; 120
26548Kelong Zhu; Christopher A. O'Keefe; V. Nicholas Vukotic; Robert W. Schurko; Stephen J. Loeb
A molecular shuttle that operates inside a metal-organic framework
Nature Chemistry, 2015, 7, 514-519
1520107 CIFAg0.2 Cd0.75 In2.1 Te4I -4 2 m6.22687; 6.22687; 12.47448
90; 90; 90
483.684Welzmiller, Simon; Hennersdorf, Felix; Schlegel, Robert; Fitch, Andrew; Wagner, Gerald; Oeckler, Oliver
Silver Indium Telluride Semiconductors and Their Solid Solutions with Cadmium Indium Telluride: Structure and Physical Properties.
Inorganic chemistry, 2015, 54, 5745-5756
1520108 CIFAg0.5 In2.5 Te4I -4 2 m6.20368; 6.20368; 12.43258
90; 90; 90
478.476Welzmiller, Simon; Hennersdorf, Felix; Schlegel, Robert; Fitch, Andrew; Wagner, Gerald; Oeckler, Oliver
Silver Indium Telluride Semiconductors and Their Solid Solutions with Cadmium Indium Telluride: Structure and Physical Properties.
Inorganic chemistry, 2015, 54, 5745-5756
1520109 CIFAg0.8 In2.4 Te4P -4 2 c6.24929; 6.24929; 12.49988
90; 90; 90
488.166Welzmiller, Simon; Hennersdorf, Felix; Schlegel, Robert; Fitch, Andrew; Wagner, Gerald; Oeckler, Oliver
Silver Indium Telluride Semiconductors and Their Solid Solutions with Cadmium Indium Telluride: Structure and Physical Properties.
Inorganic chemistry, 2015, 54, 5745-5756
1520110 CIFAg0.25 Cd0.5 In2.25 Te4I -4 2 m6.21342; 6.21342; 12.45643
90; 90; 90
480.9Welzmiller, Simon; Hennersdorf, Felix; Schlegel, Robert; Fitch, Andrew; Wagner, Gerald; Oeckler, Oliver
Silver Indium Telluride Semiconductors and Their Solid Solutions with Cadmium Indium Telluride: Structure and Physical Properties.
Inorganic chemistry, 2015, 54, 5745-5756
1520111 CIFC21 H26 N2 O4P 1 21 18.82965; 10.54451; 9.86508
90; 90.6454; 90
918.42Zhang, Dong-Bo; Yu, Dao-Geng; Sun, Meng; Zhu, Xu-Xin; Yao, Xiao-Jun; Zhou, Shuang-Yan; Chen, Jian-Jun; Gao, Kun
Ervatamines A-I, Anti-inflammatory Monoterpenoid Indole Alkaloids with Diverse Skeletons from Ervatamia hainanensis.
Journal of natural products, 2015, 78, 1253-1261
1520112 CIFC22 H32 N2 O4P 21 21 216.33312; 12.6666; 25.6966
90; 90; 90
2061.36Zhang, Dong-Bo; Yu, Dao-Geng; Sun, Meng; Zhu, Xu-Xin; Yao, Xiao-Jun; Zhou, Shuang-Yan; Chen, Jian-Jun; Gao, Kun
Ervatamines A-I, Anti-inflammatory Monoterpenoid Indole Alkaloids with Diverse Skeletons from Ervatamia hainanensis.
Journal of natural products, 2015, 78, 1253-1261
1520113 CIFC24 H30 Ge SiP 1 21/c 110.4814; 19.1943; 12.056
90; 109.021; 90
2293Zaitsev, Kirill V.; Lermontova, Elmira Kh.; Churakov, Andrei V.; Tafeenko, Viktor A.; Tarasevich, Boris N.; Poleshchuk, Oleg Kh.; Kharcheva, Anastasia V.; Magdesieva, Tatiana V.; Nikitin, Oleg M.; Zaitseva, Galina S.; Karlov, Sergey S.
Compounds of Group 14 Elements with an Element‒Element (E = Si, Ge, Sn) Bond: Effect of the Nature of the Element Atom
Organometallics, 2015, 34, 2765
1520114 CIFC24 H30 Ge2P 1 21/c 110.6888; 19.3569; 12.29
90; 109.624; 90
2395.13Zaitsev, Kirill V.; Lermontova, Elmira Kh.; Churakov, Andrei V.; Tafeenko, Viktor A.; Tarasevich, Boris N.; Poleshchuk, Oleg Kh.; Kharcheva, Anastasia V.; Magdesieva, Tatiana V.; Nikitin, Oleg M.; Zaitseva, Galina S.; Karlov, Sergey S.
Compounds of Group 14 Elements with an Element‒Element (E = Si, Ge, Sn) Bond: Effect of the Nature of the Element Atom
Organometallics, 2015, 34, 2765
1520115 CIFC42 H48 Ge3 Si2P 1 21/n 111.0225; 21.7372; 16.6855
90; 92.4892; 90
3994Zaitsev, Kirill V.; Lermontova, Elmira Kh.; Churakov, Andrei V.; Tafeenko, Viktor A.; Tarasevich, Boris N.; Poleshchuk, Oleg Kh.; Kharcheva, Anastasia V.; Magdesieva, Tatiana V.; Nikitin, Oleg M.; Zaitseva, Galina S.; Karlov, Sergey S.
Compounds of Group 14 Elements with an Element‒Element (E = Si, Ge, Sn) Bond: Effect of the Nature of the Element Atom
Organometallics, 2015, 34, 2765
1520116 CIFC28 H19 NP -19.0455; 9.563; 11.529
103.716; 98.763; 98.986
938.1Liu, Xingyan; Li, Xiaoyu; Liu, Hu; Guo, Qiang; Lan, Jingbo; Wang, Ruilin; You, Jingsong
Aldehyde as a Traceless Directing Group for Rh(III)-Catalyzed C-H Activation: A Facile Access to Diverse Indolo[1,2-a]quinolines.
Organic letters, 2015, 17, 2936-2939
1520117 CIFC17.5 H18 F8 I O3.5 S2P -18.9435; 12.1892; 12.2642
63.163; 87.526; 77.6
1162.92Matsuzaki, Kohei; Okuyama, Kenta; Tokunaga, Etsuko; Saito, Norimichi; Shiro, Motoo; Shibata, Norio
Synthesis of Diaryliodonium Salts Having Pentafluorosulfanylarenes and Their Application to Electrophilic Pentafluorosulfanylarylation of C-, O-, N-, and S-Nucleophiles.
Organic letters, 2015, 17, 3038-3041
1520118 CIFC11 H12 O5P 1 21/n 14.7531; 15.683; 14.17
90; 90.383; 90
1056.2Sinha, A. S.; Rao Khandavilli, U. B.; O’Connor, E. L.; Deadman, B. J.; Maguire, A. R.; Lawrence, S. E.
Novel co-crystals of the nutraceutical sinapic acid
CrystEngComm, 2015, 17, 4832
1520119 CIFC17 H18 N2 O6P -14.9109; 9.1732; 18.814
99.563; 94.601; 90.531
832.9Sinha, A. S.; Rao Khandavilli, U. B.; O’Connor, E. L.; Deadman, B. J.; Maguire, A. R.; Lawrence, S. E.
Novel co-crystals of the nutraceutical sinapic acid
CrystEngComm, 2015, 17, 4832
1520120 CIFC17 H16 N2 O5P 1 21/c 114.893; 31.878; 6.5992
90; 95.192; 90
3120.2Sinha, A. S.; Rao Khandavilli, U. B.; O'Connor, E. L.; Deadman, B. J.; Maguire, A. R.; Lawrence, S. E.
Novel co-crystals of the nutraceutical sinapic acid
CrystEngComm, 2015, 17, 4832
1520121 CIFC22 H28 N4 O6 SP -18.2922; 10.5857; 14.7818
98.274; 94.315; 105.62
1227.7Sinha, A. S.; Rao Khandavilli, U. B.; O'Connor, E. L.; Deadman, B. J.; Maguire, A. R.; Lawrence, S. E.
Novel co-crystals of the nutraceutical sinapic acid
CrystEngComm, 2015, 17, 4832
1520122 CIFC22 H28 N4 O6 SP -18.452; 10.605; 14.9134
98.535; 94.47; 104.13
1272.82Sinha, A. S.; Rao Khandavilli, U. B.; O'Connor, E. L.; Deadman, B. J.; Maguire, A. R.; Lawrence, S. E.
Novel co-crystals of the nutraceutical sinapic acid
CrystEngComm, 2015, 17, 4832
1520123 CIFC78 H74 Co2 Dy2 N4 O24C 1 2/c 124.102; 16.905; 22.71
90; 120.96; 90
7935Wu, Jianfeng; Zhao, Lang; Zhang, Peng; Zhang, Li; Guo, Mei; Tang, Jinkui
Linear 3d-4f compounds: synthesis, structure, and determination of the d-f magnetic interaction.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11935-11942
1520124 CIFC76 H70 Cu2 Dy2 N4 O26C 1 2/c 123.592; 16.697; 23.137
90; 119.867; 90
7904Wu, Jianfeng; Zhao, Lang; Zhang, Peng; Zhang, Li; Guo, Mei; Tang, Jinkui
Linear 3d-4f compounds: synthesis, structure, and determination of the d-f magnetic interaction.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11935-11942
1520125 CIFC78 H76 Dy2 N4 Ni2 O25C 1 2/c 124.03; 16.831; 22.733
90; 121.087; 90
7874Wu, Jianfeng; Zhao, Lang; Zhang, Peng; Zhang, Li; Guo, Mei; Tang, Jinkui
Linear 3d-4f compounds: synthesis, structure, and determination of the d-f magnetic interaction.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11935-11942
1520126 CIFC76 H70 Dy2 N4 O24 Zn2C 1 2/c 123.874; 16.89; 22.915
90; 120.515; 90
7960Wu, Jianfeng; Zhao, Lang; Zhang, Peng; Zhang, Li; Guo, Mei; Tang, Jinkui
Linear 3d-4f compounds: synthesis, structure, and determination of the d-f magnetic interaction.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11935-11942
1520127 CIFC78 H74 Co2 Gd2 N4 O25C 1 2/c 124.175; 16.937; 22.73
90; 121.179; 90
7963Wu, Jianfeng; Zhao, Lang; Zhang, Peng; Zhang, Li; Guo, Mei; Tang, Jinkui
Linear 3d-4f compounds: synthesis, structure, and determination of the d-f magnetic interaction.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11935-11942
1520128 CIFC74 H66 Cu2 Gd2 N4 O24C 1 2/c 123.668; 16.575; 23.13
90; 119.671; 90
7884Wu, Jianfeng; Zhao, Lang; Zhang, Peng; Zhang, Li; Guo, Mei; Tang, Jinkui
Linear 3d-4f compounds: synthesis, structure, and determination of the d-f magnetic interaction.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11935-11942
1520129 CIFC78 H78 Gd2 N4 Ni2 O26C 1 2/c 124.011; 16.677; 22.589
90; 121.27; 90
7731Wu, Jianfeng; Zhao, Lang; Zhang, Peng; Zhang, Li; Guo, Mei; Tang, Jinkui
Linear 3d-4f compounds: synthesis, structure, and determination of the d-f magnetic interaction.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11935-11942
1520130 CIFC76 H70 Gd2 N4 O24 Zn2C 1 2/c 123.749; 16.59; 22.922
90; 120.225; 90
7803Wu, Jianfeng; Zhao, Lang; Zhang, Peng; Zhang, Li; Guo, Mei; Tang, Jinkui
Linear 3d-4f compounds: synthesis, structure, and determination of the d-f magnetic interaction.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11935-11942
1520131 CIFC78 H74 Co2 N4 O24 Tb2C 1 2/c 124.168; 16.9669; 22.816
90; 121.013; 90
8018.4Wu, Jianfeng; Zhao, Lang; Zhang, Peng; Zhang, Li; Guo, Mei; Tang, Jinkui
Linear 3d-4f compounds: synthesis, structure, and determination of the d-f magnetic interaction.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11935-11942
1520132 CIFC78 H72 N4 Ni2 O25 Tb2C 1 2/c 124.177; 16.899; 22.727
90; 121.326; 90
7932Wu, Jianfeng; Zhao, Lang; Zhang, Peng; Zhang, Li; Guo, Mei; Tang, Jinkui
Linear 3d-4f compounds: synthesis, structure, and determination of the d-f magnetic interaction.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11935-11942
1520133 CIFC76 H70 N4 O24 Tb2 Zn2C 1 2/c 123.847; 16.792; 23.04
90; 120.204; 90
7974Wu, Jianfeng; Zhao, Lang; Zhang, Peng; Zhang, Li; Guo, Mei; Tang, Jinkui
Linear 3d-4f compounds: synthesis, structure, and determination of the d-f magnetic interaction.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11935-11942
1520134 CIFC78 H74 Co2 N4 O26 Y2C 1 2/c 124.133; 17.0815; 22.658
90; 121.233; 90
7986.5Wu, Jianfeng; Zhao, Lang; Zhang, Peng; Zhang, Li; Guo, Mei; Tang, Jinkui
Linear 3d-4f compounds: synthesis, structure, and determination of the d-f magnetic interaction.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11935-11942
1520135 CIFC74 H66 Cu2 N4 O24 Y2C 1 2/c 123.53; 16.641; 23.044
90; 119.75; 90
7834Wu, Jianfeng; Zhao, Lang; Zhang, Peng; Zhang, Li; Guo, Mei; Tang, Jinkui
Linear 3d-4f compounds: synthesis, structure, and determination of the d-f magnetic interaction.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11935-11942
1520136 CIFC78 H74 N4 Ni2 O24 Y2C 1 2/c 124.185; 17.062; 22.656
90; 121.363; 90
7983Wu, Jianfeng; Zhao, Lang; Zhang, Peng; Zhang, Li; Guo, Mei; Tang, Jinkui
Linear 3d-4f compounds: synthesis, structure, and determination of the d-f magnetic interaction.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11935-11942
1520137 CIFC74 H62 Cu2 N4 O22 Tb2C 1 2/c 123.8031; 16.5092; 23.023
90; 119.934; 90
7840.4Wu, Jianfeng; Zhao, Lang; Zhang, Peng; Zhang, Li; Guo, Mei; Tang, Jinkui
Linear 3d-4f compounds: synthesis, structure, and determination of the d-f magnetic interaction.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 11935-11942
1520138 CIFC36 H42 Cu N4 O3P 21 21 2110.0943; 15.9068; 19.5472
90; 90; 90
3138.7Faggi, Enrico; Gavara, Raquel; Bolte, Michael; Fajarí, Lluís; Juliá, Luís; Rodríguez, Laura; Alfonso, Ignacio
Copper(ii) complexes of macrocyclic and open-chain pseudopeptidic ligands: synthesis, characterization and interaction with dicarboxylates.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12700-12710
1520139 CIFC34 H38 N4 O2P 19.631; 10.027; 15.551
86.83; 87.67; 78.27
1467.5Faggi, Enrico; Gavara, Raquel; Bolte, Michael; Fajarí, Lluís; Juliá, Luís; Rodríguez, Laura; Alfonso, Ignacio
Copper(ii) complexes of macrocyclic and open-chain pseudopeptidic ligands: synthesis, characterization and interaction with dicarboxylates.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 12700-12710
1520200 CIFMn O4 WP 1 2/c 14.7983; 5.708; 4.9747
90; 91.124; 90
136.22Ruiz-Fuertes, J.; Friedrich, A.; Gomis, O.; Errandonea, D.; Morgenroth, W.; Sans, J. A.; Santamaría-Pérez, D.
High-pressure structural phase transition in MnWO4
Physical Review B, 2015, 91, 104109
1520201 CIFMn O4 WP 1 2/c 14.6888; 5.536; 4.8844
90; 91.415; 90
126.75Ruiz-Fuertes, J.; Friedrich, A.; Gomis, O.; Errandonea, D.; Morgenroth, W.; Sans, J. A.; Santamaría-Pérez, D.
High-pressure structural phase transition in MnWO4
Physical Review B, 2015, 91, 104109
1520202 CIFMn O4 WP 1 2/c 14.6644; 5.468; 4.8614
90; 91.603; 90
123.94Ruiz-Fuertes, J.; Friedrich, A.; Gomis, O.; Errandonea, D.; Morgenroth, W.; Sans, J. A.; Santamaría-Pérez, D.
High-pressure structural phase transition in MnWO4
Physical Review B, 2015, 91, 104109
1520213 CIFC46 H40 N12 O2 Zn4P -110.283; 10.474; 20.857
95.09; 94.25; 96.25
2216.3Cheng, Gang; So, Gary Kwok-Ming; To, Wai-Pong; Chen, Yong; Kwok, Chi-Chung; Ma, Chensheng; Guan, Xiangguo; Chang, Xiaoyong; Kwok, Wai-Ming; Che, Chi-Ming
Luminescent zinc(ii) and copper(i) complexes for high-performance solution-processed monochromic and white organic light-emitting devices
Chem. Sci., 2015, 6, 4623
1520214 CIFC42 H48 B9 Cu N2 O P2P -110.828; 13.677; 14.95
90.64; 106.555; 95.534
2110.6Cheng, Gang; So, Gary Kwok-Ming; To, Wai-Pong; Chen, Yong; Kwok, Chi-Chung; Ma, Chensheng; Guan, Xiangguo; Chang, Xiaoyong; Kwok, Wai-Ming; Che, Chi-Ming
Luminescent zinc(ii) and copper(i) complexes for high-performance solution-processed monochromic and white organic light-emitting devices
Chem. Sci., 2015, 6, 4623
1520215 CIFC53 H52 B9 Cl2 Cu N2 P2P 1 21/c 115.5324; 15.5957; 20.6244
90; 98.789; 90
4937.4Cheng, Gang; So, Gary Kwok-Ming; To, Wai-Pong; Chen, Yong; Kwok, Chi-Chung; Ma, Chensheng; Guan, Xiangguo; Chang, Xiaoyong; Kwok, Wai-Ming; Che, Chi-Ming
Luminescent zinc(ii) and copper(i) complexes for high-performance solution-processed monochromic and white organic light-emitting devices
Chem. Sci., 2015, 6, 4623
1520217 CIFC33 H38 N4 O6P 21 21 2111.4867; 12.742; 20.9942
90; 90; 90
3072.8Dufour-Gallant, Julien; Chatenet, David; Lubell, William D.
De Novo Conception of Small Molecule Modulators Based on Endogenous Peptide Ligands: Pyrrolodiazepin-2-one γ-Turn Mimics That Differentially Modulate Urotensin II Receptor-Mediated Vasoconstriction ex Vivo.
Journal of medicinal chemistry, 2015, 58, 4624-4637
1520218 CIFC21 H27 Cl N2 O10 S2P 21 21 2112.1222; 12.1222; 16.3859
90; 90; 90
2407.9Liu, Yang; Li, Xiao-Ming; Meng, Ling-Hong; Jiang, Wen-Li; Xu, Gang-Ming; Huang, Cai-Guo; Wang, Bin-Gui
Bisthiodiketopiperazines and Acorane Sesquiterpenes Produced by the Marine-Derived Fungus Penicillium adametzioides AS-53 on Different Culture Media.
Journal of natural products, 2015, 78, 1294-1299
1520219 CIFC20 H30 O4P 21 21 217.4701; 9.9307; 24.744
90; 90; 90
1835.6Corlay, Nina; Lecsö-Bornet, Marylin; Leborgne, Erell; Blanchard, Florent; Cachet, Xavier; Bignon, Jérôme; Roussi, Fanny; Butel, Marie-Jose; Awang, Khalijah; Litaudon, Marc
Antibacterial Labdane Diterpenoids from Vitex vestita.
Journal of natural products, 2015, 78, 1348-1356
1520220 CIFC24 H19 NC 1 2/c 142.784; 6.0454; 31.552
90; 119.951; 90
7071Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong
Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade.
Organic letters, 2015, 17, 2984-2987
1520221 CIFC30 H23 NP 1 21/c 112.0216; 6.2012; 30.083
90; 101.315; 90
2199Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong
Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade.
Organic letters, 2015, 17, 2984-2987
1520222 CIFC23 H19 NC 1 2/c 129.558; 6.041; 19.696
90; 104.661; 90
3402.4Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong
Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade.
Organic letters, 2015, 17, 2984-2987
1520223 CIFC14 H16 Cl3 N O3P 3216.1172; 16.1172; 5.6393
90; 90; 120
1268.63Skvorcova, Marija; Grigorjeva, Liene; Jirgensons, Aigars
Tetrahydro-1,3-oxazepines via Intramolecular Amination of Cyclopropylmethyl Cation.
Organic letters, 2015, 17, 2902-2904
1520224 CIFC22 H22 N4 O2 SP 1 21 110.363; 9.318; 11.453
90; 112.7; 90
1020.3Wang, Linqing; Yang, Dongxu; Li, Dan; Wang, Rui
Catalytic Enantioselective Ring-Opening and Ring-Closing Reactions of 3-Isothiocyanato Oxindoles and N-(2-Picolinoyl)aziridines.
Organic letters, 2015, 17, 3004-3007
1520225 CIFC13 H21 N3 O3P 1 21/c 14.5905; 23.474; 13.2529
90; 91.746; 90
1427.4Martínez, Luís; Martorell, Gabriel; Sampedro, Ángel; Ballester, Pablo; Costa, Antoni; Rotger, Carmen
Hydrogen Bonded Squaramide-Based Foldable Module Induces Both β- and α-Turns in Hairpin Structures of α-Peptides in Water.
Organic letters, 2015, 17, 2980-2983
1520226 CIFC5 H11 Cl N6P m n a6.4782; 9.5193; 14.311
90; 90; 90
882.5Xu, Jun; Yu, Hongde; Yang, Liulin; Wu, Guanglu; Wang, Zhiqiang; Wang, Dong; Zhang, Xi
Self-assembling 1D core/shell microrods by the introduction of additives: a one-pot and shell-tunable method
Chem. Sci., 2015, 6, 4907
1520227 CIFC58 H55 B F24 Fe N P3P 1 21/c 118.4232; 13.0618; 25.9802
90; 99.53; 90
6165.6Lindley, Brian M.; Swidan, Ala'aeddeen; Lobkovsky, Emil B.; Wolczanski, Peter T.; Adelhardt, Mario; Sutter, Jörg; Meyer, Karsten
Fe(iv) alkylidenes via protonation of Fe(ii) vinyl chelates and a comparative Mössbauer spectroscopic study
Chem. Sci., 2015, 6, 4730
1520228 CIFC61 H60 B F24 Fe N O P3C 1 2/m 119.963; 17.492; 19.586
90; 93.869; 90
6824Lindley, Brian M.; Swidan, Ala'aeddeen; Lobkovsky, Emil B.; Wolczanski, Peter T.; Adelhardt, Mario; Sutter, Jörg; Meyer, Karsten
Fe(iv) alkylidenes via protonation of Fe(ii) vinyl chelates and a comparative Mössbauer spectroscopic study
Chem. Sci., 2015, 6, 4730
1520229 CIFC58 H45 B F24 Fe N2 P2P 1 21/c 119.6517; 12.5655; 25.3645
90; 109.745; 90
5895.1Lindley, Brian M.; Swidan, Ala'aeddeen; Lobkovsky, Emil B.; Wolczanski, Peter T.; Adelhardt, Mario; Sutter, Jörg; Meyer, Karsten
Fe(iv) alkylidenes via protonation of Fe(ii) vinyl chelates and a comparative Mössbauer spectroscopic study
Chem. Sci., 2015, 6, 4730
1520230 CIFC26 H32 Fe N2 P2P -110.2138; 10.6014; 12.4208
88.674; 67.062; 89.687
1238.24Lindley, Brian M.; Swidan, Ala'aeddeen; Lobkovsky, Emil B.; Wolczanski, Peter T.; Adelhardt, Mario; Sutter, Jörg; Meyer, Karsten
Fe(iv) alkylidenes via protonation of Fe(ii) vinyl chelates and a comparative Mössbauer spectroscopic study
Chem. Sci., 2015, 6, 4730
1520261 CIFC20 H20 Cl F N4 O3P n a 2122.318; 10.108; 9.029
90; 90; 90
2036.9Areias, L. R. P.; Ruivo, E. F. P.; Gonçalves, L. M.; Duarte, M. T.; André, V.; Moreira, R.; Lucas, S. D.; Guedes, R. C.
A unified approach toward the rational design of selective low nanomolar human neutrophil elastase inhibitors
RSC Advances, 2015, 5, 51717-51721
1520262 CIFC14 H18 N2 O4 SP 21 21 216.702; 11.902; 18.892
90; 90; 90
1507Areias, L. R. P.; Ruivo, E. F. P.; Gonçalves, L. M.; Duarte, M. T.; André, V.; Moreira, R.; Lucas, S. D.; Guedes, R. C.
A unified approach toward the rational design of selective low nanomolar human neutrophil elastase inhibitors
RSC Advances, 2015, 5, 51717-51721
1520263 CIFC16 H18 N4 O2 SP 1 21 18.2251; 10.3695; 9.9358
90; 94.251; 90
845.095Deshpande, Sudhindra H.; Shende, Vaishali S.; Shingote, Savita K.; Chakravarty, Debamitra; Puranik, Vedavati G.; Chaudhari, Raghunath V.; Kelkar, Ashutosh A.
Rhodium complex with unsymmetrical vicinal diamine ligand: excellent catalyst for asymmetric transfer hydrogenation of ketones
RSC Advances, 2015, 5, 51722-51729
1520292 CIFC11 H14 Cl N O SP 1 21 15.615; 10.35; 11.29
90; 102.9; 90
640Chen, Xiao-Yang; Sun, Li-Sen; Gao, Xiang; Sun, Xing-Wen
Diastereoselective Allylation ofN-tert-Butanesulfinyl Imines: An Asymmetric Synthesis Experiment for the Undergraduate Organic Laboratory
Journal of Chemical Education, 2015, 92, 714
1520293 CIFC5 H5 Br2 NP c a 2114.2564; 4.6063; 10.7577
90; 90; 90
706.45Rumyantsev, Misha; Sitnikov, Nikolay S.; Somov, Nikolay V.
Hydrogen-bond-assisted organocatalytic acetalization of secondary alcohols: experimental and theoretical studies.
The journal of physical chemistry. A, 2015, 119, 4108-4117
1520294 CIFC7 H10 Cl NP b c a7.3965; 14.3362; 14.5021
90; 90; 90
1537.77Rumyantsev, Misha; Sitnikov, Nikolay S.; Somov, Nikolay V.
Hydrogen-bond-assisted organocatalytic acetalization of secondary alcohols: experimental and theoretical studies.
The journal of physical chemistry. A, 2015, 119, 4108-4117
1520295 CIFC5 H7 Br2 Cl N2 OP 1 21/n 110.8192; 16.9726; 6.8298
90; 130.762; 90
949.9Rumyantsev, Misha; Sitnikov, Nikolay S.; Somov, Nikolay V.
Hydrogen-bond-assisted organocatalytic acetalization of secondary alcohols: experimental and theoretical studies.
The journal of physical chemistry. A, 2015, 119, 4108-4117
1520296 CIFB0.6 La10 N1.4 O24.6 Si5.4P 63/m9.66584; 9.66584; 7.19
90; 90; 120
581.75Xia, Zhiguo; Molokeev, Maxim S.; Im, Won Bin; Unithrattil, Sanjith; Liu, Quanlin
Crystal Structure and Photoluminescence Evolution of La5(Si2+xB1‒x)(O13‒xNx):Ce3+Solid Solution Phosphors
The Journal of Physical Chemistry C, 2015, 119, 9488
1520297 CIFC52 H60 Br N4 O18 S2C 1 2/c 126.6011; 19.037; 14.4208
90; 114.731; 90
6633Carrasco-Ruiz, Anayeli; Tiburcio, Jorge
Electrostatic Kinetic Barriers in the Threading/Dethreading Motion of a Rotaxane-like Complex.
Organic letters, 2015, 17, 1858-1861
1520298 CIFC52 H86 N4 O32 S2P 1 21/n 111.8381; 23.4128; 11.8991
90; 107.339; 90
3148.12Carrasco-Ruiz, Anayeli; Tiburcio, Jorge
Electrostatic Kinetic Barriers in the Threading/Dethreading Motion of a Rotaxane-like Complex.
Organic letters, 2015, 17, 1858-1861
1520299 CIFC22 H23 I O3P 21 21 215.7232; 10.8546; 32.913
90; 90; 90
2044.7Merad, Jérémy; Borkar, Prashant; Bouyon Yenda, Tracy; Roux, Christèle; Pons, Jean-Marc; Parrain, Jean-Luc; Chuzel, Olivier; Bressy, Cyril
Highly Enantioselective Acylation of Acyclic Meso 1,3-Diols through Synergistic Isothiourea-Catalyzed Desymmetrization/Chiroablative Kinetic Resolution.
Organic letters, 2015, 17, 2118-2121
1520300 CIFC36 H46 N4 O2P -17.1052; 14.1156; 16.3735
105.153; 91.858; 102.309
1541.85Meehan, Eileen; Li, Ruoshi; Zeller, Matthias; Brückner, Christian
Octaethyl-1,3-oxazinochlorin: A β-Octaethylchlorin Analogue Made by Pyrrole Expansion.
Organic letters, 2015, 17, 2210-2213
1520301 CIFC41 H58.333 N5 OP 1 21/c 126.0651; 15.2582; 9.5468
90; 96.584; 90
3771.8Meehan, Eileen; Li, Ruoshi; Zeller, Matthias; Brückner, Christian
Octaethyl-1,3-oxazinochlorin: A β-Octaethylchlorin Analogue Made by Pyrrole Expansion.
Organic letters, 2015, 17, 2210-2213
1520302 CIFC33 H31 Br2 N O6P 1 21/c 118.4779; 9.1189; 19.3437
90; 109.352; 90
3075.2Tang, Shaojian; Park, Jong Yeun; Yeagley, Andrew A.; Sabat, Michal; Chruma, Jason J.
Decarboxylative Generation of 2-Azaallyl Anions: 2-Iminoalcohols via a Decarboxylative Erlenmeyer Reaction.
Organic letters, 2015, 17, 2042-2045
1520303 CIFC13 H23 Cl N2 NiP 1 21/n 111.1164; 12.6843; 11.5897
90; 118.363; 90
1438.02Shields, Jason D.; Gray, Erin E.; Doyle, Abigail G.
A modular, air-stable nickel precatalyst.
Organic letters, 2015, 17, 2166-2169
1520304 CIFC66.33 H81.67 N2 O4 YbP 21 21 2115.592; 20.5827; 60.065
90; 90; 90
19276.4Zeng, Chao; Yuan, Dan; Zhao, Bei; Yao, Yingming
Highly Enantioselective Epoxidation of α,β-Unsaturated Ketones Catalyzed by Rare-Earth Amides [(Me3Si)2N]3RE(μ-Cl)Li(THF)3 with Phenoxy-Functionalized Chiral Prolinols.
Organic letters, 2015, 17, 2242-2245
1520305 CIFC6 H9 N O4C 1 2/c 116.4651; 6.6186; 14.9686
90; 109.033; 90
1542Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520306 CIFC12 H19 N O3P 1 21/c 111.0623; 9.4884; 11.6015
90; 90.961; 90
1217.56Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520307 CIFC10 H16 B F2 N O3P -19.5474; 11.4938; 11.5223
92.227; 96.964; 91.605
1253.45Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520308 CIFC12 H20 B F2 N O3P 1 21/n 17.8638; 14.0418; 12.6427
90; 91.6599; 90
1395.45Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520309 CIFC12 H18 B F2 N O3P 1 21 114.7772; 11.1085; 16.6848
90; 92.405; 90
2736.4Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520310 CIFC13 H20 B F2 N O3P 1 21/n 110.6399; 11.8723; 11.9174
90; 107.028; 90
1439.41Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520311 CIFC12 H18 B F2 N O4P -111.3963; 11.7254; 12.5468
74.986; 64.116; 64.237
1353.47Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520312 CIFC10 H16 B F2 N O4I b a 212.1721; 49.556; 8.341
90; 90; 90
5031.3Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520313 CIFC10 H16 B F2 N O4P -17.0022; 7.7079; 12.3657
83.232; 83.476; 76.265
641.26Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520314 CIFC10 H17 N O4P -17.8792; 8.1476; 10.2749
106.191; 106.585; 104.538
566.58Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520315 CIFC12 H20 B F2 N O4P b c a16.8311; 9.1985; 18.0999
90; 90; 90
2802.24Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520316 CIFC12 H18 B Br2 F2 N O4P 1 21/c 110.3517; 15.7916; 9.5485
90; 99.476; 90
1539.59Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520317 CIFC8 H11 Br O4P 1 21/c 18.8688; 18.0772; 6.0396
90; 94.753; 90
964.96Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520318 CIFC19 H23.6 B F2 N2 O5.3P b c n12.2584; 10.1061; 31.0115
90; 90; 90
3841.8Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520319 CIFC19 H23 B F2 N2 O5P 1 21/n 115.4609; 8.0727; 15.6576
90; 103.611; 90
1899.36Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520320 CIFC30 H25 N2 O4 PP 1 21/c 112.5638; 14.8917; 13.7164
90; 104.477; 90
2484.8Yamamura, Masaki; Takizawa, Hiroyuki; Nabeshima, Tatsuya
Zwitterionic N2O2-Type Protonated Dipyrrin Bearing a Phosphate Anionic Moiety as a pH-Responsive Fluorescence Indicator.
Organic letters, 2015, 17, 3114-3117
1520321 CIFB Ga O3R -3 c :H4.5659; 4.5659; 14.1764
90; 90; 120
255.947Wang, Shichao; Ye, Ning; Poeppelmeier, Kenneth
Flux Growth and Crystal Structure Refinement of Calcite Type Borate GaBO3
Crystals, 2015, 5, 252
1520322 CIFC76 H72 Cu6 Ge N24 O64 W12P -111.6025; 15.9736; 15.9849
104.371; 91.222; 100.534
2814.5Pache, Aroa; Reinoso, Santiago; Felices, Leire; Iturrospe, Amaia; Lezama, Luis; Gutiérrez-Zorrilla, Juan
Single-Crystal to Single-Crystal Reversible Transformations Induced by Thermal Dehydration in Keggin-Type Polyoxometalates Decorated with Copper(II)-Picolinate Complexes: The Structure Directing Role of Guanidinium
Inorganics, 2015, 3, 194
1520323 CIFC46 H62 Cu3.5 N19 O59 Si W12P -111.9426; 12.8151; 30.0533
101.508; 90.346; 105.544
4333.58Pache, Aroa; Reinoso, Santiago; Felices, Leire; Iturrospe, Amaia; Lezama, Luis; Gutiérrez-Zorrilla, Juan
Single-Crystal to Single-Crystal Reversible Transformations Induced by Thermal Dehydration in Keggin-Type Polyoxometalates Decorated with Copper(II)-Picolinate Complexes: The Structure Directing Role of Guanidinium
Inorganics, 2015, 3, 194
1520324 CIFC76 H88 Cu6 Ge N24 O72 W12P -111.711; 15.9628; 17.0341
107.057; 94.372; 100.971
2958.92Pache, Aroa; Reinoso, Santiago; Felices, Leire; Iturrospe, Amaia; Lezama, Luis; Gutiérrez-Zorrilla, Juan
Single-Crystal to Single-Crystal Reversible Transformations Induced by Thermal Dehydration in Keggin-Type Polyoxometalates Decorated with Copper(II)-Picolinate Complexes: The Structure Directing Role of Guanidinium
Inorganics, 2015, 3, 194
1520325 CIFC76 H72 Cu6 N24 O64 Si W12P -111.6039; 15.9379; 15.9984
104.292; 91.168; 100.599
2811.55Pache, Aroa; Reinoso, Santiago; Felices, Leire; Iturrospe, Amaia; Lezama, Luis; Gutiérrez-Zorrilla, Juan
Single-Crystal to Single-Crystal Reversible Transformations Induced by Thermal Dehydration in Keggin-Type Polyoxometalates Decorated with Copper(II)-Picolinate Complexes: The Structure Directing Role of Guanidinium
Inorganics, 2015, 3, 194
1520326 CIFC76 H88 Cu6 N24 O72 Si W12P -111.7014; 15.9523; 17.0285
107.102; 94.393; 101.008
2952.16Pache, Aroa; Reinoso, Santiago; Felices, Leire; Iturrospe, Amaia; Lezama, Luis; Gutiérrez-Zorrilla, Juan
Single-Crystal to Single-Crystal Reversible Transformations Induced by Thermal Dehydration in Keggin-Type Polyoxometalates Decorated with Copper(II)-Picolinate Complexes: The Structure Directing Role of Guanidinium
Inorganics, 2015, 3, 194
1520327 CIFC45 H84 Br Mo6 N3 O18 SP 1 21/n 111.03023; 16.9232; 32.4507
90; 98.8238; 90
5985.78Healey, Merinda; Best, Stephen; Goerigk, Lars; Ritchie, Chris
A Heteroaromatically Functionalized Hexamolybdate
Inorganics, 2015, 3, 82
1520328 CIFC26 H22 Br N SP 1 21/n 112.5989; 11.5694; 15.267
90; 101.954; 90
2177.09Healey, Merinda; Best, Stephen; Goerigk, Lars; Ritchie, Chris
A Heteroaromatically Functionalized Hexamolybdate
Inorganics, 2015, 3, 82
1520379 CIFC25 H32 O5P 1 21 18.7283; 25.8978; 10.1531
90; 109.86; 90
2158.55Zhou, Haibo; Li, Liyuan; Wang, Wei; Che, Qian; Li, Dehai; Gu, Qianqun; Zhu, Tianjiao
Chrodrimanins I and J from the Antarctic Moss-Derived Fungus Penicillium funiculosum GWT2-24.
Journal of natural products, 2015, 78, 1442-1445
1520380 CIFC26 H34 O6P 1 21 18.1342; 18.9651; 15.1089
90; 102.491; 90
2275.62Zhou, Haibo; Li, Liyuan; Wang, Wei; Che, Qian; Li, Dehai; Gu, Qianqun; Zhu, Tianjiao
Chrodrimanins I and J from the Antarctic Moss-Derived Fungus Penicillium funiculosum GWT2-24.
Journal of natural products, 2015, 78, 1442-1445
1520381 CIFC21 H31 N3 O2P 1 n 14.6265; 5.6189; 38.026
90; 90.753; 90
988.43Nakane, Yuta; Takeda, Takashi; Hoshino, Norihisa; Sakai, Ken-Ichi; Akutagawa, Tomoyuki
Cation-Anion Dual Sensing of a Fluorescent Quinoxalinone Derivative Using Lactam-Lactim Tautomerism.
The journal of physical chemistry. A, 2015, 119, 6223-6231
1520382 CIFC44 H67 I Li N7 O5P -19.7164; 12.2827; 20.5362
89.4219; 77.1355; 72.4856
2274.31Nakane, Yuta; Takeda, Takashi; Hoshino, Norihisa; Sakai, Ken-Ichi; Akutagawa, Tomoyuki
Cation-Anion Dual Sensing of a Fluorescent Quinoxalinone Derivative Using Lactam-Lactim Tautomerism.
The journal of physical chemistry. A, 2015, 119, 6223-6231
1520383 CIFC37 H67 Cl N4 O2P 1 21/c 17.72739; 52.0258; 28.9218
90; 93.4544; 90
11606.1Nakane, Yuta; Takeda, Takashi; Hoshino, Norihisa; Sakai, Ken-Ichi; Akutagawa, Tomoyuki
Cation-Anion Dual Sensing of a Fluorescent Quinoxalinone Derivative Using Lactam-Lactim Tautomerism.
The journal of physical chemistry. A, 2015, 119, 6223-6231
1520384 CIFC37 H66 N4 O4P -18.0639; 16.5724; 29.689
79.436; 86.017; 89.75
3890.8Nakane, Yuta; Takeda, Takashi; Hoshino, Norihisa; Sakai, Ken-Ichi; Akutagawa, Tomoyuki
Cation-Anion Dual Sensing of a Fluorescent Quinoxalinone Derivative Using Lactam-Lactim Tautomerism.
The journal of physical chemistry. A, 2015, 119, 6223-6231
1520385 CIFC41 H45 Cl2 N5 O18P -118.718; 20.1801; 21.555
63.466; 65.8; 82.646
6629.1Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K.
β-Decamethoxysapphyrin and Its N-Benzyl Analogue.
Organic letters, 2015, 17, 3030-3033
1520386 CIFC48 H53 N5 O16 S2P 1 21/n 19.5948; 11.7166; 43.6295
90; 91.392; 90
4903.3Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K.
β-Decamethoxysapphyrin and Its N-Benzyl Analogue.
Organic letters, 2015, 17, 3030-3033
1520387 CIFC48 H51 N5 O13 SP 1 21/c 110.656; 38.925; 11.435
90; 111.21; 90
4422Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K.
β-Decamethoxysapphyrin and Its N-Benzyl Analogue.
Organic letters, 2015, 17, 3030-3033
1520388 CIFC22 H19 N O2P 21 21 218.6008; 10.6881; 18.1
90; 90; 90
1663.9Battini, Narsaiah; Battula, Satyanarayana; Kumar, Raju Ranjith; Ahmed, Qazi Naveed
2-Oxo Driven Unconventional reactions: Microwave Assisted Approaches to Tetrahydrofuro[3,2-d]oxazoles and Furanones.
Organic letters, 2015, 17, 2992-2995
1520389 CIFC36 H53 N2 O5P 21 21 219.576; 13.43; 26.522
90; 90; 90
3410.9Takemoto, Yusa; Yamamoto, Takayuki; Ikuma, Naohiko; Uchida, Yoshiaki; Suzuki, Katsuaki; Shimono, Satoshi; Takahashi, Hiroki; Sato, Nobuhiro; Oba, Yojiro; Inoue, Rintaro; Sugiyama, Masaaki; Tsue, Hirohito; Kato, Tatsuhisa; Yamauchi, Jun; Tamura, Rui
Preparation, characterization and magnetic behavior of a spin-labelled physical hydrogel containing a chiral cyclic nitroxide radical unit fixed inside the gelator molecule.
Soft matter, 2015, 11, 5563-5570
1520439 CIFC26 H18 B Cl2 F8 N3P 1 21/c 17.923; 11.039; 27.77
90; 96.981; 90
2410.8Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520440 CIFC26.14 H22.79 B Cl0.79 F2 N3 O3.24P 1 21/c 113.159; 12.065; 15.082
90; 98.075; 90
2370.7Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520441 CIFC707 H656 B16 F32 N48 O9P 1 21/c 115.429; 41.602; 24.49
90; 91.209; 90
15716Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520442 CIFC35.79 H27.57 B Cl1.57 F2 N3C 1 2/c 133.021; 10.588; 23.034
90; 132.89; 90
5900Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520443 CIFC32 H24 B Cl2 F2 N3P -17.3425; 11.0127; 15.884
94.772; 97.467; 91.375
1268.3Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520444 CIFC50.45 H44.9 B Cl2.9 F2 N3P 1 21/c 18.0911; 21.853; 25.007
90; 97.291; 90
4385.9Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520445 CIFC23 H18 B F2 N3P 1 21/n 19.594; 8.7428; 21.526
90; 100.795; 90
1773.6Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520446 CIFC16 H15 N O2 S2P c a 2118.773; 7.8448; 20.3148
90; 90; 90
2991.8Siva Reddy, Alla; Kumara Swamy, K. C.
Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.
Organic letters, 2015, 17, 2996-2999
1520447 CIFC16 H14 F N O2 S2P 1 21/c 115.7817; 13.0488; 7.2719
90; 92.391; 90
1496.2Siva Reddy, Alla; Kumara Swamy, K. C.
Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.
Organic letters, 2015, 17, 2996-2999
1520448 CIFC16 H15 N O3 S2P -19.7686; 10.4236; 16.0412
90.974; 91.846; 107.681
1554.8Siva Reddy, Alla; Kumara Swamy, K. C.
Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.
Organic letters, 2015, 17, 2996-2999
1520449 CIFC16 H15 N O2 S SeP b c a7.38023; 12.875; 31.8273
90; 90; 90
3024.24Siva Reddy, Alla; Kumara Swamy, K. C.
Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.
Organic letters, 2015, 17, 2996-2999
1520450 CIFC17 H17 N O2 S2P 1 21/n 16.63588; 12.9255; 19.0476
90; 93.665; 90
1630.41Siva Reddy, Alla; Kumara Swamy, K. C.
Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.
Organic letters, 2015, 17, 2996-2999
1520451 CIFC40 H32 N2P 1 21/n 112.149; 7.34; 16.53
90; 101.456; 90
1444.7Xu, Feng; Peng, Lifen; Shinohara, Kenta; Nishida, Takanori; Wakamatsu, Kan; Uejima, Motoyuki; Sato, Tohru; Tanaka, Kazuyoshi; Machida, Norihiko; Akashi, Haruo; Orita, Akihiro; Otera, Junzo
One-Shot Double Amination of Sondheimer-Wong Diynes: Synthesis of Photoluminescent Dinaphthopentalenes.
Organic letters, 2015, 17, 3014-3017
1520452 CIFC24 H17 N4 OP 1 21/n 13.9114; 20.5945; 22.458
90; 91.758; 90
1808.2Matuschek, David; Eusterwiemann, Steffen; Stegemann, Linda; Doerenkamp, Carsten; Wibbeling, Birgit; Daniliuc, Constantin G.; Doltsinis, Nikos L.; Strassert, Cristian A.; Eckert, Hellmut; Studer, Armido
Profluorescent verdazyl radicals ‒ synthesis and characterization
Chem. Sci., 2015, 6, 4712
1520453 CIFC28 H19 N4 OP 1 21 111.7763; 5.828; 16.1543
90; 104.773; 90
1072.06Matuschek, David; Eusterwiemann, Steffen; Stegemann, Linda; Doerenkamp, Carsten; Wibbeling, Birgit; Daniliuc, Constantin G.; Doltsinis, Nikos L.; Strassert, Cristian A.; Eckert, Hellmut; Studer, Armido
Profluorescent verdazyl radicals ‒ synthesis and characterization
Chem. Sci., 2015, 6, 4712
1520454 CIFC32 H26 N4 OP 1 21/c 17.474; 9.2641; 35.865
90; 91.227; 90
2482.7Matuschek, David; Eusterwiemann, Steffen; Stegemann, Linda; Doerenkamp, Carsten; Wibbeling, Birgit; Daniliuc, Constantin G.; Doltsinis, Nikos L.; Strassert, Cristian A.; Eckert, Hellmut; Studer, Armido
Profluorescent verdazyl radicals ‒ synthesis and characterization
Chem. Sci., 2015, 6, 4712
1520455 CIFC36 H28 N4 OP 1 21/c 111.2158; 10.0647; 24.8459
90; 97.414; 90
2781.25Matuschek, David; Eusterwiemann, Steffen; Stegemann, Linda; Doerenkamp, Carsten; Wibbeling, Birgit; Daniliuc, Constantin G.; Doltsinis, Nikos L.; Strassert, Cristian A.; Eckert, Hellmut; Studer, Armido
Profluorescent verdazyl radicals ‒ synthesis and characterization
Chem. Sci., 2015, 6, 4712
1520456 CIFC21 H17 Br F3 N O2P 21 21 219.1964; 13.4028; 15.611
90; 90; 90
1924.2Zhang, Xiao; Liu, Wen-Bo; Tu, Hang-Fei; You, Shu-Li
Ligand-enabled Ir-catalyzed intermolecular diastereoselective and enantioselective allylic alkylation of 3-substituted indoles
Chem. Sci., 2015, 6, 4525
1520484 CIFC42 H59 N2 O5 YP 1 21/n 111.5994; 17.3406; 20.277
90; 101.616; 90
3995Gu, Weikai; Xu, Pengfei; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Shen, Qi
Synthesis and Characterization of Yttrium and Ytterbium Complexes Supported by Salen Ligands and Their Catalytic Properties forrac-Lactide Polymerization
Organometallics, 2015, 34, 2907
1520485 CIFC42 H59 N2 O5 YbP 1 21/n 111.6286; 17.386; 20.275
90; 101.788; 90
4012.6Gu, Weikai; Xu, Pengfei; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Shen, Qi
Synthesis and Characterization of Yttrium and Ytterbium Complexes Supported by Salen Ligands and Their Catalytic Properties forrac-Lactide Polymerization
Organometallics, 2015, 34, 2907
1520486 CIFC42 H55 Cl4 N2 O5 YP 1 21/n 111.801; 20.57; 18.885
90; 104.53; 90
4437.6Gu, Weikai; Xu, Pengfei; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Shen, Qi
Synthesis and Characterization of Yttrium and Ytterbium Complexes Supported by Salen Ligands and Their Catalytic Properties forrac-Lactide Polymerization
Organometallics, 2015, 34, 2907
1520487 CIFC45 H55 Cl4 N2 O4 YbC 1 2/c 124.1809; 15.0796; 25.3731
90; 102.719; 90
9025Gu, Weikai; Xu, Pengfei; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Shen, Qi
Synthesis and Characterization of Yttrium and Ytterbium Complexes Supported by Salen Ligands and Their Catalytic Properties forrac-Lactide Polymerization
Organometallics, 2015, 34, 2907
1520488 CIFC50 H75 N2 O3 YP -110.5853; 12.7151; 19.2574
89.476; 76.593; 74.104
2420.77Gu, Weikai; Xu, Pengfei; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Shen, Qi
Synthesis and Characterization of Yttrium and Ytterbium Complexes Supported by Salen Ligands and Their Catalytic Properties forrac-Lactide Polymerization
Organometallics, 2015, 34, 2907
1520489 CIFC36 H43 Cl4 N2 O4 YbP -111.1518; 14.3086; 14.3249
110.668; 112.05; 101.601
1829.7Gu, Weikai; Xu, Pengfei; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Shen, Qi
Synthesis and Characterization of Yttrium and Ytterbium Complexes Supported by Salen Ligands and Their Catalytic Properties forrac-Lactide Polymerization
Organometallics, 2015, 34, 2907
1520490 CIFC101 H141 N4 O6 Y2P -115.7733; 17.1095; 20.0984
93.832; 99.873; 110.235
4967Gu, Weikai; Xu, Pengfei; Wang, Yaorong; Yao, Yingming; Yuan, Dan; Shen, Qi
Synthesis and Characterization of Yttrium and Ytterbium Complexes Supported by Salen Ligands and Their Catalytic Properties forrac-Lactide Polymerization
Organometallics, 2015, 34, 2907
1520491 CIFC60 H74 N4 O4P -111.2497; 12.373; 20.0241
95.185; 106.067; 94.622
2651.1Xia, Debin; Marszalek, Tomasz; Li, Mengmeng; Guo, Xin; Baumgarten, Martin; Pisula, Wojciech; Müllen, Klaus
Solution-Processable n-Type Organic Semiconductors Based on Angular-Shaped 2-(12H-Dibenzofluoren-12-ylidene)malononitrilediimide.
Organic letters, 2015, 17, 3074-3077
1520492 CIFC13 H10 Cl N3 O2P b c a7.24; 11.439; 29.79
90; 90; 90
2467Xia, Guomin; Ruan, Chengyan; Wang, Hongming
Highly sensitive detection of carbon dioxide by a pyrimido[1,2-a]benzimidazole derivative: combining experimental and theoretical studies.
The Analyst, 2015, 140, 5099-5104
1520493 CIFC30 H26 Co F6 N6 O7 S2P -111.0341; 12.5779; 13.0044
82.865; 88.796; 66.687
1643.85Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520494 CIFC29 H35 F6 N7 O12 S2 ZnP 1 21/n 113.0156; 12.7488; 22.3963
90; 92.294; 90
3713.3Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520495 CIFC36 H42 Co F6 N6 O11 S2P 1 21/n 112.4657; 15.6171; 21.316
90; 91.047; 90
4149.1Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520496 CIFC30 H30 F6 N6 O11 S2 ZnP -114.707; 21.388; 25.657
67.683; 75.282; 89.683
7184Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520497 CIFC30 H32.5 F6 N6 O10 S2 ZnP -111.0677; 13.3087; 13.5558
71.591; 78.668; 67.235
1740.65Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520498 CIFC29 H27.5 Co F6 N7 O9.25 S2P -113.2461; 20.9848; 26.9609
111.361; 96.713; 94.455
6872.7Jurss, Jonah W.; Khnayzer, Rony S.; Panetier, Julien A.; El Roz, Karim A.; Nichols, Eva M.; Head-Gordon, Martin; Long, Jeffrey R.; Castellano, Felix N.; Chang, Christopher J.
Bioinspired design of redox-active ligands for multielectron catalysis: effects of positioning pyrazine reservoirs on cobalt for electro- and photocatalytic generation of hydrogen from water
Chem. Sci., 2015, 6, 4954
1520499 CIFC37.35 H42.46 Cl2 N6 O3.88 RuP -110.4996; 13.3012; 13.4802
80.434; 82.981; 86.221
1840.52Tong, Lianpeng; Zong, Ruifa; Zhou, Rongwei; Kaveevivitchai, Nattawut; Zhang, Gang; Thummel, Randolph P.
Ruthenium catalysts for water oxidation involving tetradentate polypyridine-type ligands.
Faraday discussions, 2015, 185, 87-104
1520502 CIFC37 H20 F4 N4 O4P 1 21/c 122.674; 10.0584; 13.4593
90; 99.514; 90
3027.4Zhang, Jian; Jin, Jianyong; Cooney, Ralph; Fu, Qiang; Qiao, Greg G.; Thomas, Sylvie; Merkel, Tim C.
Synthesis of perfectly alternating copolymers for polymers of intrinsic microporosity
Polym. Chem., 2015, 6, 5003
1520504 CIFC20 H16 I N OP -110.699; 11.726; 22.2683
94.284; 101.795; 109.369
2549Wang, Jia; Zhu, Hai-Tao; Qiu, Yi-Feng; Niu, Yuan; Chen, Si; Li, Ying-Xiu; Liu, Xue-Yuan; Liang, Yong-Min
Facile Synthesis of Carbazoles via a Tandem Iodocyclization with 1,2-Alkyl Migration and Aromatization.
Organic letters, 2015, 17, 3186-3189
1520505 CIFC20 H16 I N OP b c a7.2355; 20.9295; 23.0167
90; 90; 90
3485.5Wang, Jia; Zhu, Hai-Tao; Qiu, Yi-Feng; Niu, Yuan; Chen, Si; Li, Ying-Xiu; Liu, Xue-Yuan; Liang, Yong-Min
Facile Synthesis of Carbazoles via a Tandem Iodocyclization with 1,2-Alkyl Migration and Aromatization.
Organic letters, 2015, 17, 3186-3189
1520506 CIFC30 H24 Cl4 N2 O2 ZnC 1 2/c 121.692; 4.8468; 28.611
90; 111.442; 90
2799.9Men, Guangwen; Chen, Chunrong; Liang, Chunshuang; Han, Wenkun; Jiang, Shimei
A novel cascade strategy with supramolecular and chemodosimetric methods for designing a fluorescent ratiometric detector hypersensitive to trace water.
The Analyst, 2015, 140, 5454-5458
1520507 CIFC42 H86 N4 O6P -14.7746; 5.4698; 44.772
91.162; 91.821; 96.985
1159.66Zhong, Di-Chang; Liao, Lie-Qiang; Wang, Ke-Jun; Liu, Hui-Jin; Luo, Xu-Zhong
Heat-set gels formed from easily accessible gelators of a succinamic acid derivative (SAD) and a primary alkyl amine (R-NH2).
Soft matter, 2015, 11, 6386-6392
1520513 CIFC24 H24P 1 21/n 17.4014; 30.606; 7.739
90; 100.806; 90
1722Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520514 CIFC20 H24 O4 SP 1 n 111.2988; 5.7063; 14.045
90; 102.129; 90
885.3Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520515 CIFC25 H29 N O5 SF d d 222.419; 52.094; 7.523
90; 90; 90
8786Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520516 CIFC25 H29 N O5 SC 1 2/c 130.166; 11.6914; 14.2065
90; 113.297; 90
4601.9Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520517 CIFC19 H19 F OP 21 21 218.4903; 9.6656; 18.663
90; 90; 90
1531.6Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520518 CIFC43 H41 N3 O4P 1 21/c 131.617; 15.428; 14.478
90; 101.899; 90
6910Zhang, Feng-Lian; Zhu, Xu; Chiba, Shunsuke
Tf~2~NH-Catalyzed Amide Synthesis from Vinyl Azides and Alcohols
Organic Letters, 2015, 17, 3138-3141
1520519 CIFC13 H12 Cl N O4P 21 21 217.9023; 12.49; 12.9
90; 90; 90
1273.2Sekikawa, Tohru; Kitaguchi, Takayuki; Kitaura, Hayato; Minami, Tatsuya; Hatanaka, Yasuo
Catalytic Activity of epi-Quinine-Derived 3,5-Bis(trifluoromethyl)benzamide in Asymmetric Nitro-Michael Reaction of Furanones.
Organic letters, 2015, 17, 3026-3029
1520520 CIFC39 H40 B F2 N3 O4P -18.745; 10.225; 20.19
89.48; 86.38; 65.669
1641.4Hiruta, Yuki; Koiso, Hikaru; Ozawa, Hitoshi; Sato, Hiroyasu; Hamada, Kensaku; Yabushita, Satoshi; Citterio, Daniel; Suzuki, Koji
Near IR Emitting Red-Shifting Ratiometric Fluorophores Based on Borondipyrromethene.
Organic letters, 2015, 17, 3022-3025
1520521 CIFC37.5 H36.5 B Cl1.5 F2 N3 O4P -18.776; 10.567; 19.225
84.193; 82.204; 69.585
1652.6Hiruta, Yuki; Koiso, Hikaru; Ozawa, Hitoshi; Sato, Hiroyasu; Hamada, Kensaku; Yabushita, Satoshi; Citterio, Daniel; Suzuki, Koji
Near IR Emitting Red-Shifting Ratiometric Fluorophores Based on Borondipyrromethene.
Organic letters, 2015, 17, 3022-3025
1520522 CIFC46 H44 B2 N2 O2P 1 21/c 17.274; 17.864; 15.322
90; 100.332; 90
1958.7Kubota, Yasuhiro; Niwa, Takahiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki
Synthesis, Absorption, and Electrochemical Properties of Quinoid-Type Bisboron Complexes with Highly Symmetrical Structures.
Organic letters, 2015, 17, 3174-3177
1520523 CIFC42 H36 B2 N2 O2P 1 21/c 17.054; 17.672; 13.751
90; 96.406; 90
1703.5Kubota, Yasuhiro; Niwa, Takahiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki
Synthesis, Absorption, and Electrochemical Properties of Quinoid-Type Bisboron Complexes with Highly Symmetrical Structures.
Organic letters, 2015, 17, 3174-3177
1520524 CIFC53 H69 N6 O25 P2 RuP n n a21.3561; 19.4016; 14.9635
90; 90; 90
6200.01Fielden, John; Sumliner, Jordan M.; Han, Nannan; Geletii, Yurii V.; Xiang, Xu; Musaev, Djamaladdin G.; Lian, Tianquan; Hill, Craig L.
Water splitting with polyoxometalate-treated photoanodes: enhancing performance through sensitizer design
Chem. Sci., 2015, 6, 5531
1520525 CIFC34 H20 Co2 N2 O8P -112.956; 13.122; 13.752
84.973; 67.595; 83.245
2144.1Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520526 CIFC17 H10 Co N O4P -17.7116; 10.2889; 11.0085
71.43; 86.282; 82.265
820.22Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520527 CIFC34 H20 Co2 N2 O8P -112.9698; 13.1304; 13.7579
85.041; 68.014; 83.544
2156.3Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520528 CIFC17 H10 Co N O4P -17.6397; 10.4311; 10.9968
71.121; 87.061; 83.361
823.5Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520529 CIFC51 H30 Co3 N3 O12C 1 2 117.173; 19.784; 13.887
90; 95.771; 90
4694Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520530 CIFC51 H30 Co3 N3 O12C 1 2 117.0391; 20.0278; 13.8334
90; 96.243; 90
4692.7Aggarwal, Himanshu; Das, Raj Kumar; Bhatt, Prashant M.; Barbour, Leonard J.
Isolation of a structural intermediate during switching of degree of interpenetration in a metal‒organic framework
Chem. Sci., 2015, 6, 4986
1520531 CIFC13 H8 Br Mn N2 O5P 1 21/c 115.1341; 13.1528; 7.0537
90; 98.591; 90
1388.33Walsh, James J.; Smith, Charlotte L.; Neri, Gaia; Whitehead, George F. S.; Robertson, Craig M.; Cowan, Alexander J.
FDCDU15 - Carbon Dioxide Utilisation: Improving the efficiency of electrochemical CO2 reduction using immobilized manganese complexes
Faraday Discuss., 2015
1520532 CIFC23 H26 Br Mn N2 O10P -16.52291; 13.1864; 16.0537
102.912; 95.846; 98.607
1317.59Walsh, James J.; Smith, Charlotte L.; Neri, Gaia; Whitehead, George F. S.; Robertson, Craig M.; Cowan, Alexander J.
FDCDU15 - Carbon Dioxide Utilisation: Improving the efficiency of electrochemical CO2 reduction using immobilized manganese complexes
Faraday Discuss., 2015
1520533 CIFC15 H16 O2P -17.5962; 8.0111; 10.4017
111.355; 93.168; 90.2112
588.43Park, Jung-Woo; Kou, Kevin G. M.; Kim, Daniel K.; Dong, Vy M.
Rh-Catalyzed Desymmetrization of α-Quaternary Centers by Isomerization-Hydroacylation.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 4479-4483
1520534 CIFC20 H20 N4 O4P 17.9466; 14.9541; 16.2556
78.9198; 79.5663; 82.7612
1856Park, Jung-Woo; Kou, Kevin G. M.; Kim, Daniel K.; Dong, Vy M.
Rh-Catalyzed Desymmetrization of α-Quaternary Centers by Isomerization-Hydroacylation.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 4479-4483
1520535 CIFC41 H46 N4 S2C 1 2/c 124.1082; 18.137; 16.7624
90; 106.002; 90
7045.4Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520536 CIFC65 H64 B2 N4 S2I 41/a :241.594; 41.594; 13.1413
90; 90; 90
22735.2Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520537 CIFC71 H56 B2 F20 N4 O2 S2P 1 21/c 114.5445; 22.7136; 19.7133
90; 98.039; 90
6448.4Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520538 CIFC42 H49 B N2 S3P -16.3487; 16.1168; 19.3671
74.649; 85.857; 83.373
1896.4Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520539 CIFC32 H45 B N2 S3P -16.524; 13.6675; 18.0034
98.64; 95.792; 101.67
1539.9Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520540 CIFC30 H39 B Br2 N2 S3P -110.2773; 12.1331; 14.8059
65.908; 79.793; 68.09
1563Crossley, D. L.; Cade, I. A.; Clark, E. R.; Escande, A.; Humphries, M. J.; King, S. M.; Vitorica-Yrezabal, I.; Ingleson, M. J.; Turner, M. L.
Enhancing electron affinity and tuning band gap in donor‒acceptor organic semiconductors by benzothiadiazole directed C‒H borylation
Chem. Sci., 2015, 6, 5144
1520542 CIFC32 H25 N O4P 1 21 16.62144; 20.1343; 9.362
90; 100.915; 90
1225.54Zhao, Shuai; Zhao, Yuan-Yuan; Lin, Jun-Bing; Xie, Ting; Liang, Yong-Min; Xu, Peng-Fei
Organocatalyzed Asymmetric Vinylogous Allylic-Allylic Alkylation of Morita-Baylis-Hillman Carbonates with Olefinic Azlactones: Facile Access to Chiral Multifunctional α-Amino Acid Derivatives.
Organic letters, 2015, 17, 3206-3209
1520543 CIFC25 H20 Au Br F3 PP 21 21 218.3781; 14.3827; 19.3153
90; 90; 90
2327.49Martínez-Salvador, Sonia; Falvello, Larry R.; Martín, Antonio; Menjón, Babil
A hexanuclear gold carbonyl cluster
Chem. Sci., 2015, 6, 5506
1520544 CIFC27 H22 Au2 Br Cl2 F6 PP 1 21/n 111.2208; 16.168; 17.031
90; 108.049; 90
2937.7Martínez-Salvador, Sonia; Falvello, Larry R.; Martín, Antonio; Menjón, Babil
A hexanuclear gold carbonyl cluster
Chem. Sci., 2015, 6, 5506
1520545 CIFC56 H40 Au6 Br2 F18 O2 P2C 1 2/m 111.61; 23.9064; 11.1568
90; 97.975; 90
3066.66Martínez-Salvador, Sonia; Falvello, Larry R.; Martín, Antonio; Menjón, Babil
A hexanuclear gold carbonyl cluster
Chem. Sci., 2015, 6, 5506
1520546 CIFS3 TiP 1 21/m 14.9476; 3.3787; 8.7479
90; 97.617; 90
144.944Lipatov, Alexey; Wilson, Peter M.; Shekhirev, Mikhail; Teeter, Jacob D.; Netusil, Ross; Sinitskii, Alexander
Few-layered titanium trisulfide (TiS3) field-effect transistors.
Nanoscale, 2015, 7, 12291-12296
1520547 CIFC25 H24 SP -19.4128; 9.6074; 12.0794
97.999; 97.992; 108.357
1007.08Zhang, Hang; Wang, Bo; Yi, Heng; Zhang, Yan; Wang, Jianbo
Rh(II)-Catalyzed [2,3]-Sigmatropic Rearrangement of Sulfur Ylides Derived from Cyclopropenes and Sulfides.
Organic letters, 2015, 17, 3322-3325
1520552 CIFC36 H22 N12P 1 21/n 115.3809; 11.5149; 17.7975
90; 90.677; 90
3151.9Saltsman, Irena; Goldberg, Israel; Gross, Zeev
Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.
Organic letters, 2015, 17, 3214-3217
1520553 CIFC35 H19 F4 N6 O2 PI b a 221.689; 29.869; 10.7143
90; 90; 90
6941Saltsman, Irena; Goldberg, Israel; Gross, Zeev
Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.
Organic letters, 2015, 17, 3214-3217
1520554 CIFC51 H33 Co F4 N8P 1 21/c 112.3996; 15.4999; 21.5037
90; 97.248; 90
4099.8Saltsman, Irena; Goldberg, Israel; Gross, Zeev
Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.
Organic letters, 2015, 17, 3214-3217
1520555 CIFC24 H20 Br2 N2C 1 2/c 116.3504; 14.9527; 9.2389
90; 92.387; 90
2256.8Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520556 CIFC24 H18 N2P -19.4274; 12.3411; 15.5934
83.302; 82.714; 79.24
1759.9Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520557 CIFC62 H50 Ag2 N4 O6 S2P 1 21/c 114.33; 10.8862; 17.8919
90; 110.048; 90
2622Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520558 CIFC50 H36 Ag2 F6 N4 O6 S2P -110.3809; 10.9748; 11.0438
109.43; 98.185; 97.328
1153.7Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520559 CIFC50 H36 Ag2 F6 N4 O6 S2P -110.4495; 11.0503; 11.0576
109.671; 96.586; 97.962
1172.8Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520560 CIFC62 H50 Ag2 N4 O6 S2P 1 21/c 114.369; 10.925; 18.106
90; 110.574; 90
2661Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520561 CIFC51 H58 F6 O14 S2P -111.2709; 11.7647; 20.1194
88.271; 83.035; 86.352
2642.1Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520562 CIFC46 H46 Cl2 F6 O14 S2P 1 n 111.616; 18.2419; 11.617
90; 94.1589; 90
2455.14Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520563 CIFC48.75 H55.04 Cl2.25 F3 O12 SP n a 2135.9931; 12.0648; 11.369
90; 90; 90
4937Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520564 CIFC51 H58 F6 O14 S2P 21 21 2111.3045; 12.1357; 37.187
90; 90; 90
5101.6Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520565 CIFC51 H55 F9 O16 S3P 1 21/c 122.0373; 11.9982; 22.7155
90; 110.288; 90
5633.5Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520566 CIFC51 H55 F9 O16 S3P b c a20.6289; 22.2856; 24.1696
90; 90; 90
11111.4Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520572 CIFC43 H56 O19P -18.6734; 11.1397; 11.8133
92.575; 96.635; 108.711
1069.74Lai, Yongji; Liu, Tingting; Sa, Rongjian; Wei, Xialan; Xue, Yongbo; Wu, Zhaodi; Luo, Zengwei; Xiang, Ming; Zhang, Yonghui; Yao, Guangmin
Neolignans with a Rare 2-Oxaspiro[4.5]deca-6,9-dien-8-one Motif from the Stem Bark of Cinnamomum subavenium.
Journal of natural products, 2015, 78, 1740-1744
1520573 CIFC17 H15 N SP 21 21 216.1669; 12.182; 17.8605
90; 90; 90
1341.77Hardegger, Leo A.; Habegger, Jacqueline; Donohoe, Timothy J.
Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation.
Organic letters, 2015, 17, 3222-3225
1520574 CIFC19 H17 N OP b c a7.4565; 18.3137; 20.6855
90; 90; 90
2824.73Hardegger, Leo A.; Habegger, Jacqueline; Donohoe, Timothy J.
Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation.
Organic letters, 2015, 17, 3222-3225
1520575 CIFC16 H15 N3P 1 21/m 19.7773; 6.90436; 9.79548
90; 98.985; 90
653.14Castillo, Juan-Carlos; Quiroga, Jairo; Abonia, Rodrigo; Rodriguez, Jean; Coquerel, Yoann
The Aryne aza-Diels-Alder Reaction: Flexible Syntheses of Isoquinolines.
Organic letters, 2015, 17, 3374-3377
1520576 CIFC21 H15 N3P 1 21/c 114.0946; 11.4421; 9.74761
90; 99.2056; 90
1551.77Castillo, Juan-Carlos; Quiroga, Jairo; Abonia, Rodrigo; Rodriguez, Jean; Coquerel, Yoann
The Aryne aza-Diels-Alder Reaction: Flexible Syntheses of Isoquinolines.
Organic letters, 2015, 17, 3374-3377
1520577 CIFC20 H20 O6P 21 21 2110.1756; 12.2477; 13.4918
90; 90; 90
1681.45Bautista, Elihú; Fragoso-Serrano, Mabel; Toscano, Rubén A; García-Peña, María Del Rosario; Ortega, Alfredo
Teotihuacanin, a Diterpene with an Unusual Spiro-10/6 System from Salvia amarissima with Potent Modulatory Activity of Multidrug Resistance in Cancer Cells.
Organic letters, 2015, 17, 3280-3282
1520578 CIFC56 H57 Cu3 N38 O22.5P -114.1016; 14.4022; 20.4554
94.939; 95.386; 119.157
3570.2Palomas, David; Kalamaras, Christos; Haycock, Peter; White, Andrew J. P.; Hellgardt, Klaus; Horton, Andrew; Crimmin, Mark R.
Re-evaluating selectivity as a determining factor in peroxidative methane oxidation by multimetallic copper complexes
Catal. Sci. Technol., 2015, 5, 4108
1520579 CIFC24 H52 B6 Cu4 F8 N4 O17C 1 2/c 114.4651; 19.3815; 14.1054
90; 90.991; 90
3953.9Palomas, David; Kalamaras, Christos; Haycock, Peter; White, Andrew J. P.; Hellgardt, Klaus; Horton, Andrew; Crimmin, Mark R.
Re-evaluating selectivity as a determining factor in peroxidative methane oxidation by multimetallic copper complexes
Catal. Sci. Technol., 2015, 5, 4108
1520580 CIFC84 H118 Al3 N6 O6P 1 21/n 113.8521; 24.7127; 22.886
90; 93.263; 90
7821.7Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520581 CIFC27 H37 Al N2 O2P 1 21 19.9462; 10.3018; 12.8708
90; 108.547; 90
1250.3Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520582 CIFC29 H41 Al N2 O3P 21 21 218.0191; 13.4769; 25.379
90; 90; 90
2742.77Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520583 CIFC41 H65 Al N2 O3P 1 21/c 116.6845; 19.6643; 12.0401
90; 99.106; 90
3900.4Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520584 CIFC32 H48 Hf N2 O4P 1 21/c 114.0484; 13.4118; 16.8344
90; 101.404; 90
3109.22Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520585 CIFC32 H48 Hf N2 O4P 4310.3884; 10.3884; 28.732
90; 90; 90
3100.72Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520586 CIFC32 H48 Hf N2 O4P 4110.39461; 10.39461; 28.7569
90; 90; 90
3107.12Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520587 CIFC31 H45.67 Al N2 O3P a -326.2561; 26.2561; 26.2561
90; 90; 90
18100.5Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520588 CIFC32 H48 N2 O4 TiP 1 21/c 113.7916; 12.9946; 17.548
90; 102.79; 90
3066.86Jones, Matthew D.; Brady, Lauren; McKeown, Paul; Buchard, Antoine; Schäfer, Pascal M.; Thomas, Lynne H.; Mahon, Mary F.; Woodman, Timothy J.; Lowe, John P.
Metal influence on the iso- and hetero-selectivity of complexes of bipyrrolidine derived salan ligands for the polymerisation of rac-lactide
Chem. Sci., 2015, 6, 5034
1520589 CIFC45 H70 ThP 1 c 112.658; 10.48; 18.889
90; 127; 90
2001Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520590 CIFC48 H74 ThP 1 21/n 110.699; 26.148; 17.831
90; 98.273; 90
4936Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520591 CIFC49 H72 ThP -110.468; 11.297; 18.569
80.098; 82.085; 78.986
2110.8Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520592 CIFC53 H73 N ThP -111.109; 21.888; 21.958
97.052; 90.196; 90.925
5298Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520593 CIFC53 H73 N O ThP 1 21/c 115.278; 12.306; 25.718
90; 90.308; 90
4835.2Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520594 CIFC52 H77 N O ThP -110.9616; 11.0914; 20.157
77.206; 84.115; 75.93
2315.1Fang, Bo; Zhang, Lei; Hou, Guohua; Zi, Guofu; Fang, De-Cai; Walter, Marc D.
C‒H bond activation induced by thorium metallacyclopropene complexes: a combined experimental and computational study
Chem. Sci., 2015, 6, 4897
1520595 CIFC15 H20 N2 O3P 1 21 17.9384; 7.0246; 12.9394
90; 98.464; 90
713.7Mercado-Marin, Eduardo V; Sarpong, Richmond
Unified Approach to Prenylated Indole Alkaloids: Total Syntheses of (-)-17-Hydroxy-Citrinalin B, (+)-Stephacidin A, and (+)-Notoamide I.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 5048-5052
1520596 CIFC26 H29 N3 O3P 21 21 218.7961; 9.7026; 35.0914
90; 90; 90
2994.9Mercado-Marin, Eduardo V; Sarpong, Richmond
Unified Approach to Prenylated Indole Alkaloids: Total Syntheses of (-)-17-Hydroxy-Citrinalin B, (+)-Stephacidin A, and (+)-Notoamide I.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 5048-5052
1520597 CIFC16 H12 Cl N OP 21 21 219.3918; 13.5329; 51.624
90; 90; 90
6561.3Pedroni, J.; Saget, T.; Donets, P. A.; Cramer, N.
Enantioselective palladium(0)-catalyzed intramolecular cyclopropane functionalization: access to dihydroquinolones, dihydroisoquinolones and the BMS-791325 ring system
Chem. Sci., 2015, 6, 5164
1520598 CIFC40 H62 N2 Si2P -19.4109; 10.1841; 11.6538
91.036; 102.694; 116.006
970.92Chandra Mondal, Kartik; Roy, Sudipta; Dittrich, Birger; Maity, Bholanath; Dutta, Sayan; Koley, Debasis; Vasa, Suresh Kumar; Linser, Rasmus; Dechert, Sebastian; Roesky, Herbert W.
A soluble molecular variant of the semiconducting silicondiselenide
Chem. Sci., 2015, 6, 5230
1520599 CIFC20 H31 N OP 1 21/n 19.269; 17.342; 11.775
90; 96.71; 90
1880Chandra Mondal, Kartik; Roy, Sudipta; Dittrich, Birger; Maity, Bholanath; Dutta, Sayan; Koley, Debasis; Vasa, Suresh Kumar; Linser, Rasmus; Dechert, Sebastian; Roesky, Herbert W.
A soluble molecular variant of the semiconducting silicondiselenide
Chem. Sci., 2015, 6, 5230
1520600 CIFC46 H70 N2 Si2P -112.8; 13.86; 14.36
66.45; 79.9; 67.84
2162Chandra Mondal, Kartik; Roy, Sudipta; Dittrich, Birger; Maity, Bholanath; Dutta, Sayan; Koley, Debasis; Vasa, Suresh Kumar; Linser, Rasmus; Dechert, Sebastian; Roesky, Herbert W.
A soluble molecular variant of the semiconducting silicondiselenide
Chem. Sci., 2015, 6, 5230
1520601 CIFC46 H70 N2 Si2P -112.79; 13.783; 14.433
66.35; 79.58; 67.48
2152Chandra Mondal, Kartik; Roy, Sudipta; Dittrich, Birger; Maity, Bholanath; Dutta, Sayan; Koley, Debasis; Vasa, Suresh Kumar; Linser, Rasmus; Dechert, Sebastian; Roesky, Herbert W.
A soluble molecular variant of the semiconducting silicondiselenide
Chem. Sci., 2015, 6, 5230
1520602 CIFC24 H39 N O Se2 SiP 1 21/n 114.6952; 10.08; 17.7472
90; 109.567; 90
2477.04Chandra Mondal, Kartik; Roy, Sudipta; Dittrich, Birger; Maity, Bholanath; Dutta, Sayan; Koley, Debasis; Vasa, Suresh Kumar; Linser, Rasmus; Dechert, Sebastian; Roesky, Herbert W.
A soluble molecular variant of the semiconducting silicondiselenide
Chem. Sci., 2015, 6, 5230
1520611 CIFC22 H23 F N6 O5P 1 21/c 113.8135; 13.3386; 14.0876
90; 114.496; 90
2362.04Tsou, Nancy; Shultz, C. Scott; Andreani, Teresa; Ball, Richard G.; Brunskill, Andrew; Balsells, Jaume; Cohen, Ryan D.; DaSilva, Jimmy; Li, Jing; Reamer, Robert A.; de Lera Ruiz, Manuel; Variankaval, Narayan; Varsolona, Richard J.; Yasuda, Nobuyoshi; York, Gregory
Careful Navigation of the Crystallographic Landscape of MK-8970: A Racemic Acetal Carbonate Prodrug of Raltegravir
Organic Process Research & Development, 2015, 19, 1882
1520612 CIFC25 H29 F N6 O8P 21 21 219.4933; 11.2461; 24.486
90; 90; 90
2614.2Tsou, Nancy; Shultz, C. Scott; Andreani, Teresa; Ball, Richard G.; Brunskill, Andrew; Balsells, Jaume; Cohen, Ryan D.; DaSilva, Jimmy; Li, Jing; Reamer, Robert A.; de Lera Ruiz, Manuel; Variankaval, Narayan; Varsolona, Richard J.; Yasuda, Nobuyoshi; York, Gregory
Careful Navigation of the Crystallographic Landscape of MK-8970: A Racemic Acetal Carbonate Prodrug of Raltegravir
Organic Process Research & Development, 2015, 19, 1882
1520613 CIFC25 H29 F N6 O8P 1 21/n 111.2744; 9.4324; 25.6466
90; 102.205; 90
2665.73Tsou, Nancy; Shultz, C. Scott; Andreani, Teresa; Ball, Richard G.; Brunskill, Andrew; Balsells, Jaume; Cohen, Ryan D.; DaSilva, Jimmy; Li, Jing; Reamer, Robert A.; de Lera Ruiz, Manuel; Variankaval, Narayan; Varsolona, Richard J.; Yasuda, Nobuyoshi; York, Gregory
Careful Navigation of the Crystallographic Landscape of MK-8970: A Racemic Acetal Carbonate Prodrug of Raltegravir
Organic Process Research & Development, 2015, 19, 1882
1520614 CIFC25 H23 N O3P 1 21/c 19.4141; 23.293; 9.0609
90; 92.942; 90
1984.3Brady, Patrick B.; Carreira, Erick M.
Addition of Trifluoroborates to Oxetanyl N,O-Acetals: Entry into Spiro and Fused Saturated Heterocycles.
Organic letters, 2015, 17, 3350-3353
1520615 CIFC18 H17 N O2P 1 21/c 18.0166; 15.8594; 11.2674
90; 98.788; 90
1415.7Brady, Patrick B.; Carreira, Erick M.
Addition of Trifluoroborates to Oxetanyl N,O-Acetals: Entry into Spiro and Fused Saturated Heterocycles.
Organic letters, 2015, 17, 3350-3353
1520616 CIFC37 H31 N O5P 1 21/n 111.364; 10.93; 24.447
90; 96.564; 90
3017Mo, Lei; Wu, Lin-Lin; Wang, Shaozhong; Yao, Zhu-Jun
Efficient Synthesis of Octahydrophenanthrene Derivatives with Mild Cascade Reactions of Isochromenylium Tetrafluoroborates and Bifunctional Styrenes.
Organic letters, 2015, 17, 3314-3317
1520617 CIFC41 H48 Br N7 O3P -111.7286; 15.6534; 22.6519
93.311; 99.266; 107.5
3889.5Nair, Ratish R.; Raju, M.; Patel, Neha P.; Raval, Ishan H.; Suresh, E.; Haldar, Soumya; Chatterjee, Pabitra B.
Naked eye instant reversible sensing of Cu(2+) and its in situ imaging in live brine shrimp Artemia.
The Analyst, 2015, 140, 5464-5468
1520618 CIFC56 H100 F N O4P -415.6111; 15.6111; 10.505
90; 90; 90
2560.14Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520619 CIFC22 H50 Cl2 F N O4P 1 21/c 19.9446; 18.0891; 15.7361
90; 103.523; 90
2752.27Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520620 CIFC26 H60 F N O6P b c n9.9133; 17.3454; 18.3631
90; 90; 90
3157.54Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520621 CIFC26 H60 F N O4C 1 2/c 122.5166; 14.2863; 19.8783
90; 103.626; 90
6214.47Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520622 CIFC38.39 H77.58 F N O12P 21 21 218.978; 24.2645; 10.3218
90; 90; 90
4753.1Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520623 CIFC22 H44 F0.5 N0.5 O7C 1 2 125.1923; 9.6565; 10.6715
90; 92.2457; 90
2594.06Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520624 CIFC28 H64 F N O4P b c a18.6017; 18.6158; 19.1084
90; 90; 90
6616.96Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520625 CIFC56 H64 F N O4P 21 21 2110.6859; 12.6528; 34.797
90; 90; 90
4704.78Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520626 CIFC49 H80 F N O7P 1 c 18.7551; 12.7463; 22.1115
90; 92.0698; 90
2465.93Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520627 CIFC73 H78 F N O3P -114.5683; 19.9837; 20.7534
91.2454; 94.4191; 103.901
5842.46Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520628 CIFC55 H72 F N O3P -19.4953; 12.1501; 21.4618
81.8444; 89.1604; 78.5486
2401.96Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520629 CIFC54 H68 F N O2P 1 21/n 111.2887; 17.6025; 24.966
90; 98.4318; 90
4907.35Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520630 CIFC60 H80 F N O2P -113.4717; 17.5643; 24.8506
78.8655; 80.5422; 69.645
5379Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520631 CIFC76 H96 F N3 O5C 1 2/c 127.7157; 9.7374; 25.2072
90; 105.664; 90
6550.2Engle, Keary M.; Pfeifer, Lukas; Pidgeon, George W.; Giuffredi, Guy T.; Thompson, Amber L.; Paton, Robert S.; Brown, John M.; Gouverneur, Véronique
Coordination diversity in hydrogen-bonded homoleptic fluoride‒alcohol complexes modulates reactivity
Chem. Sci., 2015, 6, 5293
1520633 CIFC22 H21 Br N2 O3 S2P b c a11.7745; 15.3391; 24.3582
90; 90; 90
4399.34Choi, Wonseok; Kim, Jaeeun; Ryu, Taekyu; Kim, Ki-Bbeum; Lee, Phil Ho
Synthesis of N-Imidoyl and N-Oxoimidoyl Sulfoximines from 1-Alkynes, N-Sulfonyl Azides, and Sulfoximines.
Organic letters, 2015, 17, 3330-3333
1520634 CIFC22 H20 N2 O4 S2P -19.0038; 10.66; 11.8108
75.2664; 76.0323; 75.5364
1042.26Choi, Wonseok; Kim, Jaeeun; Ryu, Taekyu; Kim, Ki-Bbeum; Lee, Phil Ho
Synthesis of N-Imidoyl and N-Oxoimidoyl Sulfoximines from 1-Alkynes, N-Sulfonyl Azides, and Sulfoximines.
Organic letters, 2015, 17, 3330-3333
1520635 CIFC30 H29 N O3P 21 21 217.37176; 14.7771; 21.8173
90; 90; 90
2376.63Majumdar, Nilanjana; Saito, Akira; Yin, Liang; Kumagai, Naoya; Shibasaki, Masakatsu
Direct Catalytic Asymmetric Conjugate Addition of Saturated and Unsaturated Thioamides.
Organic letters, 2015, 17, 3362-3365
1520636 CIFC29 H32 N2 S2P 1 21 110.39896; 9.11807; 13.7409
90; 108.291; 90
1237.06Majumdar, Nilanjana; Saito, Akira; Yin, Liang; Kumagai, Naoya; Shibasaki, Masakatsu
Direct Catalytic Asymmetric Conjugate Addition of Saturated and Unsaturated Thioamides.
Organic letters, 2015, 17, 3362-3365
1520637 CIFC21 H15 F O2P 1 21/c 112.0845; 5.9453; 22.597
90; 103.246; 90
1580.3Du, Xiang-Wei; Stanley, Levi M.
Tandem Alkyne Hydroacylation and Oxo-Michael Addition: Diastereoselective Synthesis of 2,3-Disubstituted Chroman-4-ones and Fluorinated Derivatives.
Organic letters, 2015, 17, 3276-3279
1520638 CIFC29 H24 Au Fe O2 P SP -19.187; 9.964; 15.554
108.411; 96.805; 95.38
1328.34Fernández-Gallardo, Jacob; Elie, Benelita T.; Sadhukha, Tanmoy; Prabha, Swayam; Sanaú, Mercedes; Rotenberg, Susan A.; Ramos, Joe W.; Contel, María
Heterometallic titanium‒gold complexes inhibit renal cancer cells in vitro and in vivo
Chem. Sci., 2015, 6, 5269
1520639 CIFC33 H29 Cl N2 O2 SP 1 21 110.1227; 25.116; 11.547
90; 97.553; 90
2910.3Wang, Yidong; Zhang, Peichao; Liu, Yuan; Xia, Fei; Zhang, Junliang
Enantioselective gold-catalyzed intermolecular [2+2] versus [4+2]-cycloadditions of 3-styrylindoles with N-allenamides: observation of interesting substituent effects
Chem. Sci., 2015, 6, 5564
1520640 CIFC35 H32 N2 O4 SP 21 21 216.0633; 11.5428; 42.4729
90; 90; 90
2972.57Wang, Yidong; Zhang, Peichao; Liu, Yuan; Xia, Fei; Zhang, Junliang
Enantioselective gold-catalyzed intermolecular [2+2] versus [4+2]-cycloadditions of 3-styrylindoles with N-allenamides: observation of interesting substituent effects
Chem. Sci., 2015, 6, 5564
1520655 CIFC32 H38 O5 Si2P 1 21/c 19.2692; 9.7098; 34.752
90; 92.266; 90
3125.3Zimmerman, Jake R.; Johntony, Olivia; Steigerwald, Daniel; Criss, Cody; Myers, Brian J.; Kinder, David H.
The Synthesis of a New Class of Highly Fluorescent Chromones via an Inverse-Demand Hetero-Diels-Alder Reaction.
Organic letters, 2015, 17, 3256-3259
1520656 CIFC16 H17 Cl O5P -16.9648; 7.7685; 14.728
76.228; 76.658; 84.002
752.04Zimmerman, Jake R.; Johntony, Olivia; Steigerwald, Daniel; Criss, Cody; Myers, Brian J.; Kinder, David H.
The Synthesis of a New Class of Highly Fluorescent Chromones via an Inverse-Demand Hetero-Diels-Alder Reaction.
Organic letters, 2015, 17, 3256-3259
1520657 CIFC18 H17 Br O5P 1 21 15.6762; 10.5443; 14.1611
90; 100.294; 90
833.92Sinha, Debarshi; Biswas, Arnab; Singh, Vinod K.
Chiral Phosphine-Silver(I) Complex Catalyzed Enantioselective Interrupted Feist-Bénary Reaction with Ynones: The Aldol-Cycloisomerization Cascade.
Organic letters, 2015, 17, 3302-3305
1520658 CIFC19 H20 N2 O6P 21 21 215.8624; 9.6327; 31.868
90; 90; 90
1799.61Chen, Shi; Ibrahim, Ahmad A.; Mondal, Mukulesh; Magee, Anthony J.; Cruz, Adam J.; Wheeler, Kraig A.; Kerrigan, Nessan J.
Asymmetric Synthesis of Deoxypropionate Derivatives via Catalytic Hydrogenolysis of Enantioenriched Z-Ketene Heterodimers.
Organic letters, 2015, 17, 3248-3251
1520659 CIFC22 H32 Cl2 I2 Si2P 1 21/n 113.1915; 9.4009; 22.0383
90; 106.275; 90
2623.49Sproul, Kyle C.; Chalifoux, Wesley A.
Highly Regio- and Diastereoselective Formation of Tetrasubstituted (Z)-1,2-Dihaloalkenes from the Halogenation of Trimethylsilyl Alkynes with ICl.
Organic letters, 2015, 17, 3334-3337
1520660 CIFC16 H10 Cl2 I2P b c a9.0806; 15.5457; 23.2185
90; 90; 90
3277.6Sproul, Kyle C.; Chalifoux, Wesley A.
Highly Regio- and Diastereoselective Formation of Tetrasubstituted (Z)-1,2-Dihaloalkenes from the Halogenation of Trimethylsilyl Alkynes with ICl.
Organic letters, 2015, 17, 3334-3337
1520661 CIFC20 H16 Br2 OP -17.1574; 11.25; 22.434
84.231; 84.177; 89.834
1787.9Li, De-Yao; Wei, Yin; Marek, Ilan; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed cycloisomerization of vinylidenecyclopropane-enes via carbene or non-carbene processes
Chem. Sci., 2015, 6, 5519
1520662 CIFC25 H36 OP 1 21/c 114.4666; 10.0707; 16.4037
90; 109.508; 90
2252.65Li, De-Yao; Wei, Yin; Marek, Ilan; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed cycloisomerization of vinylidenecyclopropane-enes via carbene or non-carbene processes
Chem. Sci., 2015, 6, 5519
1520663 CIFC28 H34 OC 1 2/c 123.302; 11.4445; 18.904
90; 104.415; 90
4882.6Li, De-Yao; Wei, Yin; Marek, Ilan; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed cycloisomerization of vinylidenecyclopropane-enes via carbene or non-carbene processes
Chem. Sci., 2015, 6, 5519
1520664 CIFC20 H16 Br2 OP -16.0698; 11.4589; 13.8421
67.027; 85.348; 76.337
861.26Li, De-Yao; Wei, Yin; Marek, Ilan; Tang, Xiang-Ying; Shi, Min
Gold(i)-catalyzed cycloisomerization of vinylidenecyclopropane-enes via carbene or non-carbene processes
Chem. Sci., 2015, 6, 5519
1520665 CIFC62 H138 Ge2 Si14C 1 2/c 138.0616; 9.3192; 48.0059
90; 92.3498; 90
17013.6Sasamori, Takahiro; Sugahara, Tomohiro; Agou, Tomohiro; Sugamata, Koh; Guo, Jing-Dong; Nagase, Shigeru; Tokitoh, Norihiro
Reaction of a diaryldigermyne with ethylene
Chem. Sci., 2015, 6, 5526
1520666 CIFC80 H162 Ge2 Si14P 1 21/a 112.7486; 20.8969; 18.9393
90; 103.248; 90
4911.28Sasamori, Takahiro; Sugahara, Tomohiro; Agou, Tomohiro; Sugamata, Koh; Guo, Jing-Dong; Nagase, Shigeru; Tokitoh, Norihiro
Reaction of a diaryldigermyne with ethylene
Chem. Sci., 2015, 6, 5526
1520667 CIFC64 H142 Ge2 Si14P b c a21.4391; 21.7284; 36.5231
90; 90; 90
17013.8Sasamori, Takahiro; Sugahara, Tomohiro; Agou, Tomohiro; Sugamata, Koh; Guo, Jing-Dong; Nagase, Shigeru; Tokitoh, Norihiro
Reaction of a diaryldigermyne with ethylene
Chem. Sci., 2015, 6, 5526
1520670 CIFC44 H28 O14P 1 21/c 119.7826; 11.0872; 30.0405
90; 95.85; 90
6554.6Cheuk, Dominic; Khamar, Dikshitkumar; McArdle, Patrick; Rasmuson, Åke C.
Solid Forms, Crystal Habits, and Solubility of Danthron
Journal of Chemical & Engineering Data, 2015, 60, 2110
1520671 CIFC15 H16 O3P 41 21 29.6557; 9.6557; 26.319
90; 90; 90
2453.8Shi, Yu-Sheng; Liu, Yun-Bao; Ma, Shuang-Gang; Li, Yong; Qu, Jing; Li, Li; Yuan, Shao-Peng; Hou, Qi; Li, Yu-Huan; Jiang, Jian-Dong; Yu, Shi-Shan
Bioactive Sesquiterpenes and Lignans from the Fruits of Xanthium sibiricum.
Journal of natural products, 2015, 78, 1526-1535
1520672 CIFC11 H14 O3P 21 21 216.1491; 8.0979; 20.2092
90; 90; 90
1006.31Shi, Yu-Sheng; Liu, Yun-Bao; Ma, Shuang-Gang; Li, Yong; Qu, Jing; Li, Li; Yuan, Shao-Peng; Hou, Qi; Li, Yu-Huan; Jiang, Jian-Dong; Yu, Shi-Shan
Bioactive Sesquiterpenes and Lignans from the Fruits of Xanthium sibiricum.
Journal of natural products, 2015, 78, 1526-1535
1520673 CIFC20 H30 O4P 21 21 217.587; 9.6985; 25.106
90; 90; 90
1847.4Xu, Jing; Sun, Yihang; Wang, Meicheng; Ren, Quanhui; Li, Shen; Wang, Hao; Sun, Xiaocong; Jin, Da-Qing; Sun, Hongwei; Ohizumi, Yasushi; Guo, Yuanqiang
Bioactive Diterpenoids from the Leaves of Callicarpa macrophylla.
Journal of natural products, 2015, 78, 1563-1569
1520674 CIFC28 H33 N3 Na O10 Re SP 1 21/c 131.609; 10.4939; 9.2829
90; 96.146; 90
3061.5Jia, Jianhua; Cui, Mengchao; Dai, Jiapei; Liu, Boli
(99m)Tc(CO)3-Labeled Benzothiazole Derivatives Preferentially Bind Cerebrovascular Amyloid: Potential Use as Imaging Agents for Cerebral Amyloid Angiopathy.
Molecular pharmaceutics, 2015, 12, 2937-2946
1520675 CIFC16 H14 N2 OP 1 21/n 113.4616; 4.959; 19.7696
90; 93.71; 90
1316.98Li, Shangda; Ji, Huafang; Cai, Lei; Li, Gang
Pd(ii)-catalyzed remote regiodivergent ortho- and meta-C‒H functionalizations of phenylethylamines
Chem. Sci., 2015, 6, 5595
1520676 CIFC20 H18 N2 O3C 1 2/c 133.97; 6.299; 16.431
90; 92.257; 90
3513Li, Shangda; Ji, Huafang; Cai, Lei; Li, Gang
Pd(ii)-catalyzed remote regiodivergent ortho- and meta-C‒H functionalizations of phenylethylamines
Chem. Sci., 2015, 6, 5595
1520682 CIFC26 H19 N3 O5 SP -110.4761; 10.8361; 11.3358
76.911; 61.867; 86.563
1103.68Rao, Wei-Hao; Zhan, Bei-Bei; Chen, Kai; Ling, Peng-Xiang; Zhang, Zhuo-Zhuo; Shi, Bing-Feng
Pd(II)-Catalyzed Direct Sulfonylation of Unactivated C(sp(3))-H Bonds with Sodium Sulfinates.
Organic letters, 2015, 17, 3552-3555
1520683 CIFC20 H24 Cl N3 OP 1 21 110.868; 6.8325; 12.6102
90; 103.793; 90
909.38Johnson, Rebecca E.; de Rond, Tristan; Lindsay, Vincent N. G.; Keasling, Jay D.; Sarpong, Richmond
Synthesis of Cycloprodigiosin Identifies the Natural Isolate as a Scalemic Mixture.
Organic letters, 2015, 17, 3474-3477
1520684 CIFC13 H17 Cl O3P n a 2128.508; 5.4891; 8.1976
90; 90; 90
1282.79Tanveer, Kashif; Jarrah, Kareem; Taylor, Mark S.
Borinic Acid Catalyzed, Regioselective Chloroacylations and Chlorosulfonylations of 2,3-Epoxy Alcohols.
Organic letters, 2015, 17, 3482-3485
1520685 CIFC21 H21 Cl O4P b c a15.5081; 11.7102; 20.245
90; 90; 90
3676.6Tanveer, Kashif; Jarrah, Kareem; Taylor, Mark S.
Borinic Acid Catalyzed, Regioselective Chloroacylations and Chlorosulfonylations of 2,3-Epoxy Alcohols.
Organic letters, 2015, 17, 3482-3485
1520686 CIFC33 H30 N2 O6 S2P -110.7946; 12.4093; 13.1553
76.627; 68.739; 81.216
1593.12Yan, Xiaonan; Ling, Fei; Zhang, Yuchen; Ma, Cheng
Three-Component Functionalized Dihydropyridine Synthesis via a Formal Inverse Electron-Demand Hetero-Diels-Alder Reaction.
Organic letters, 2015, 17, 3536-3539
1520694 CIFC33 H27 N3 O13P -111.319; 12.665; 14.597
86.284; 86.306; 68.207
1937.1Chen, Ji-Peng; He, Wei; Yang, Zhen-Yu; Yao, Zhu-Jun
Synthesis of Tricyclo[4,3,1,0(1,5)]decane Core of Plumisclerin A Using Pauson-Khand Annulation and SmI2-Mediated Radical Cyclization.
Organic letters, 2015, 17, 3379-3381
1520695 CIFC41 H29 N2 OP 21 21 219.7022; 14.1065; 22.5755
90; 90; 90
3089.78Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520696 CIFC41 H32 N2 OP b c a9.7137; 21.2283; 30.357
90; 90; 90
6259.8Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520697 CIFC28 H19 F3 N2 OP -19.7447; 10.0599; 12.2374
103.037; 100.267; 97.73
1130.75Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520698 CIFC27 H21 N O SP 1 21/n 111.5129; 21.7914; 17.1772
90; 98.718; 90
4259.66Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520699 CIFC42 H34 N2 OP 1 21/n 17.8222; 19.2845; 21.7791
90; 100.329; 90
3232.1Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520700 CIFC21 H23 N2 O RhP 1 21/n 17.9626; 12.2907; 18.1403
90; 102.579; 90
1732.7Martínez, Ángel Manu; Echavarren, Javier; Alonso, Inés; Rodríguez, Nuria; Gómez Arrayás, Ramón; Carretero, Juan C.
RhI/RhIIIcatalyst-controlled divergent aryl/heteroaryl C‒H bond functionalization of picolinamides with alkynes
Chem. Sci., 2015, 6, 5802
1520702 CIFC41 H60 N8 O3 Ti2P 1 21/n 119.8643; 9.0349; 24.8875
90; 106.793; 90
4276.1Chen, Zhou; Liu, Jinna; Pei, Hao; Liu, Wei; Chen, Yanmei; Wu, Jian; Li, Wu; Li, Yahong
Directed Amination of Aryl Methyl Ethers Mediated by Ti(NMe2)4 at Room Temperature.
Organic letters, 2015, 17, 3406-3409
1520703 CIFC163 H221 N28 O13 Ti4P -119.976; 20.518; 21.236
89.583; 78.919; 76.303
8292Chen, Zhou; Liu, Jinna; Pei, Hao; Liu, Wei; Chen, Yanmei; Wu, Jian; Li, Wu; Li, Yahong
Directed Amination of Aryl Methyl Ethers Mediated by Ti(NMe2)4 at Room Temperature.
Organic letters, 2015, 17, 3406-3409
1520704 CIFC22 H20 N2 O3P -111.7148; 11.8534; 14.1205
110; 95.83; 100.677
1781.51Dörr, Aurélie A; Lubell, William D.
γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate.
Organic letters, 2015, 17, 3592-3595
1520705 CIFC22 H22 N2 O3P c a 2117.651; 15.5231; 13.7865
90; 90; 90
3777.48Dörr, Aurélie A; Lubell, William D.
γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate.
Organic letters, 2015, 17, 3592-3595
1520706 CIFC22 H20 N2 O3P 1 21/n 115.2406; 5.6664; 20.6863
90; 94.254; 90
1781.53Dörr, Aurélie A; Lubell, William D.
γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate.
Organic letters, 2015, 17, 3592-3595
1520707 CIFC20 H23 N O8P 21 21 218.7215; 11.3257; 19.217
90; 90; 90
1898.2Paladino, Marco; Zaifman, Joshua; Ciufolini, Marco A.
Total Synthesis of (+)-3-Demethoxyerythratidinone and (+)-Erysotramidine via the Oxidative Amidation of a Phenol.
Organic letters, 2015, 17, 3422-3425
1520708 CIFC15 H15 N3 O4P 1 21/n 111.4762; 7.95324; 16.5869
90; 107.894; 90
1440.7Wang, Qi; Tang, Xuli; Luo, Xiangchao; de Voogd, Nicole J.; Li, Pinglin; Li, Guoqiang
(+)- and (-)-Spiroreticulatine, A Pair of Unusual Spiro Bisheterocyclic Quinoline-imidazole Alkaloids from the South China Sea Sponge Fascaplysinopsis reticulata.
Organic letters, 2015, 17, 3458-3461
1520709 CIFC324.95 H223.55 Cu4 N97.65 Na11.5 O115.55 S16 Zn12P 1 n 121.91216; 32.64068; 35.0386
90; 98.2694; 90
24800Giri, Chandan; Topić, Filip; Cametti, Massimo; Rissanen, Kari
Mixed valence mono- and hetero-metallic grid catenanes
Chem. Sci., 2015, 6, 5712
1520710 CIFC326.45 H230.05 Cu10 N98.15 O119.55 S16 Zn6.4P -124.6339; 26.2771; 38.566
71.189; 77.8; 87.75
23086Giri, Chandan; Topić, Filip; Cametti, Massimo; Rissanen, Kari
Mixed valence mono- and hetero-metallic grid catenanes
Chem. Sci., 2015, 6, 5712
1520711 CIFC325.25 H227.25 Cu16 N97.75 O116.25 S16P -124.6594; 26.1086; 38.5294
71.7131; 78.2731; 87.7169
23054.1Giri, Chandan; Topić, Filip; Cametti, Massimo; Rissanen, Kari
Mixed valence mono- and hetero-metallic grid catenanes
Chem. Sci., 2015, 6, 5712
1520712 CIFC80 H52 N24 O20 S4 Zn4I 41/a16.4641; 16.4641; 53.397
90; 90; 90
14474.1Giri, Chandan; Topić, Filip; Cametti, Massimo; Rissanen, Kari
Mixed valence mono- and hetero-metallic grid catenanes
Chem. Sci., 2015, 6, 5712
1520713 CIFC25 H24 N4 O4P 1 21/c 120.3743; 5.7348; 19.2424
90; 102.342; 90
2196.4Huang, Zhongxing; Sam, Quynh P.; Dong, Guangbin
Palladium-catalyzed direct β-arylation of ketones with diaryliodonium salts: a stoichiometric heavy metal-free and user-friendly approach
Chem. Sci., 2015, 6, 5491
1520714 CIFC28 H28 N2 O4 S4P 1 21/c 16.5498; 20.4037; 11.0725
90; 100.469; 90
1455.1Huang, Zhongxing; Sam, Quynh P.; Dong, Guangbin
Palladium-catalyzed direct β-arylation of ketones with diaryliodonium salts: a stoichiometric heavy metal-free and user-friendly approach
Chem. Sci., 2015, 6, 5491
1520715 CIFC28 H28 N2 O4 S4I 1 2/a 115.181; 15.559; 23.696
90; 105.016; 90
5406Huang, Zhongxing; Sam, Quynh P.; Dong, Guangbin
Palladium-catalyzed direct β-arylation of ketones with diaryliodonium salts: a stoichiometric heavy metal-free and user-friendly approach
Chem. Sci., 2015, 6, 5491
1520716 CIFC25 H45 N O2 SP 1 21/c 137.479; 7.292; 9.0925
90; 93.702; 90
2479.8Bhat, R.; Patel, H.; Tsai, P.-C.; Sun, X.-L.; Daoud, D.; Lalancette, R. A.; Michniak-Kohn, B.; Pietrangelo, A.
Effect of residue structure on the thermal and thermoresponsive properties of γ-substituted poly(N-acryloyl-2-pyrrolidones)
Polym. Chem., 2015, 6, 5993
1520720 CIFC21 H31 Cl3 O2C 1 2 122.6971; 11.6034; 19.6097
90; 124.027; 90
4280.19Wang, Li-Jun; Xiong, Juan; Liu, Shu-Ting; Pan, Li-Long; Yang, Guo-Xun; Hu, Jin-Feng
ent-Abietane-Type and Related Seco-/Nor-diterpenoids from the Rare Chloranthaceae Plant Chloranthus sessilifolius and Their Antineuroinflammatory Activities.
Journal of natural products, 2015, 78, 1635-1646
1520721 CIFC20 H32 O3P 1 21 16.1311; 17.3576; 8.5062
90; 98.395; 90
895.54Wang, Li-Jun; Xiong, Juan; Liu, Shu-Ting; Pan, Li-Long; Yang, Guo-Xun; Hu, Jin-Feng
ent-Abietane-Type and Related Seco-/Nor-diterpenoids from the Rare Chloranthaceae Plant Chloranthus sessilifolius and Their Antineuroinflammatory Activities.
Journal of natural products, 2015, 78, 1635-1646
1520722 CIFC20 H30 O4P 21 21 217.0352; 9.6018; 26.5701
90; 90; 90
1794.83Wang, Li-Jun; Xiong, Juan; Liu, Shu-Ting; Pan, Li-Long; Yang, Guo-Xun; Hu, Jin-Feng
ent-Abietane-Type and Related Seco-/Nor-diterpenoids from the Rare Chloranthaceae Plant Chloranthus sessilifolius and Their Antineuroinflammatory Activities.
Journal of natural products, 2015, 78, 1635-1646
1520723 CIFC22 H29 N3 O5P 1 21/c 113.212; 9.1505; 18.16
90; 105.195; 90
2118.7Braun, Doris E.; Koztecki, Lien H.; McMahon, Jennifer A.; Price, Sarah L.; Reutzel-Edens, Susan M
Navigating the Waters of Unconventional Crystalline Hydrates.
Molecular pharmaceutics, 2015, 12, 3069-3088
1520724 CIFC22 H28.46 N3 O4.73C 1 2/c 126.498; 9.6469; 20.342
90; 128.706; 90
4057.8Braun, Doris E.; Koztecki, Lien H.; McMahon, Jennifer A.; Price, Sarah L.; Reutzel-Edens, Susan M
Navigating the Waters of Unconventional Crystalline Hydrates.
Molecular pharmaceutics, 2015, 12, 3069-3088
1520725 CIFC22 H28.9 N3 O4.95C 1 2/c 126.663; 9.634; 20.863
90; 128.322; 90
4204Braun, Doris E.; Koztecki, Lien H.; McMahon, Jennifer A.; Price, Sarah L.; Reutzel-Edens, Susan M
Navigating the Waters of Unconventional Crystalline Hydrates.
Molecular pharmaceutics, 2015, 12, 3069-3088
1520726 CIFC44 H42 F6 N6 O7 S2P b c a21.512; 10.424; 40.881
90; 90; 90
9167Zhu, Chuan-Le; Yang, Li-Jun; Li, Shen; Zheng, Yan; Ma, Jun-An
Brine-Stabilized 2,2,2-Trifluorodiazoethane and Its Application in the Synthesis of CF3-Substituted Cyclopropane α-Amino Acids.
Organic letters, 2015, 17, 3442-3445
1520727 CIFC28 H23 F3 N2 O3P -18.882; 10.743; 14.629
87; 76.43; 65.66
1234.8Zhu, Chuan-Le; Yang, Li-Jun; Li, Shen; Zheng, Yan; Ma, Jun-An
Brine-Stabilized 2,2,2-Trifluorodiazoethane and Its Application in the Synthesis of CF3-Substituted Cyclopropane α-Amino Acids.
Organic letters, 2015, 17, 3442-3445
1520728 CIFC25 H34 N2 O9 SiP b c a10.3059; 20.6482; 25.5756
90; 90; 90
5442.4Cheng, Qing-Qing; Qian, Yu; Zavalij, Peter Y.; Doyle, Michael P.
Lewis Acid/Rhodium-Catalyzed Formal [3 + 3]-Cycloaddition of Enoldiazoacetates with Donor-Acceptor Cyclopropanes.
Organic letters, 2015, 17, 3568-3571
1520729 CIFC25 H31 N O3 S2P 1 21 16.6067; 19.709; 9.7407
90; 109.22; 90
1197.65Fernández-Valparís, Javier; Romo, Juan Manuel; Romea, Pedro; Urpí, Fèlix; Kowalski, Hubert; Font-Bardia, Mercè
Stereoselective Alkylation of (S)-N-Acyl-4-isopropyl-1,3-thiazolidine-2-thiones Catalyzed by (Me3P)2NiCl2.
Organic letters, 2015, 17, 3540-3543
1520734 CIFC15 H24 N2 O3P 21 21 217.9518; 12.143; 14.869
90; 90; 90
1435.7Pan, Qi-Ming; Li, Yu-Huan; Hua, Jing; Huang, Fu-Ping; Wang, Heng-Shan; Liang, Dong
Antiviral Matrine-Type Alkaloids from the Rhizomes of Sophora tonkinensis.
Journal of natural products, 2015, 78, 1683-1688
1520735 CIFC15 H22 N2 O3P 21 21 219.052; 10.577; 14.128
90; 90; 90
1352.7Pan, Qi-Ming; Li, Yu-Huan; Hua, Jing; Huang, Fu-Ping; Wang, Heng-Shan; Liang, Dong
Antiviral Matrine-Type Alkaloids from the Rhizomes of Sophora tonkinensis.
Journal of natural products, 2015, 78, 1683-1688
1520736 CIFC16 H16 N2 O SP 21 21 217.2412; 10.1066; 19.681
90; 90; 90
1440.33Mary Sheeba, Mani; Preethi, Sankaranarayanan; Nijamudheen, A.; Muthu Tamizh, Manoharan; Datta, Ayan; Farrugia, Louis J.; Karvembu, Ramasamy
Half-sandwich Ru(η6-C6H6) complexes with chiral aroylthioureas for enhanced asymmetric transfer hydrogenation of ketones ‒ experimental and theoretical studies
Catal. Sci. Technol., 2015, 5, 4790
1520737 CIFC14 H14 N2 O S2P 21 21 217.1805; 9.8395; 19.6096
90; 90; 90
1385.47Mary Sheeba, Mani; Preethi, Sankaranarayanan; Nijamudheen, A.; Muthu Tamizh, Manoharan; Datta, Ayan; Farrugia, Louis J.; Karvembu, Ramasamy
Half-sandwich Ru(η6-C6H6) complexes with chiral aroylthioureas for enhanced asymmetric transfer hydrogenation of ketones ‒ experimental and theoretical studies
Catal. Sci. Technol., 2015, 5, 4790
1520738 CIFC24 H25 Cl2 N3 O Ru SP 21 21 2110.0568; 14.9314; 16.7695
90; 90; 90
2518.1Mary Sheeba, Mani; Preethi, Sankaranarayanan; Nijamudheen, A.; Muthu Tamizh, Manoharan; Datta, Ayan; Farrugia, Louis J.; Karvembu, Ramasamy
Half-sandwich Ru(η6-C6H6) complexes with chiral aroylthioureas for enhanced asymmetric transfer hydrogenation of ketones ‒ experimental and theoretical studies
Catal. Sci. Technol., 2015, 5, 4790
1520739 CIFC20 H20 Cl2 N2 O Ru S2P 21 21 216.6174; 17.1016; 19.4048
90; 90; 90
2196Mary Sheeba, Mani; Preethi, Sankaranarayanan; Nijamudheen, A.; Muthu Tamizh, Manoharan; Datta, Ayan; Farrugia, Louis J.; Karvembu, Ramasamy
Half-sandwich Ru(η6-C6H6) complexes with chiral aroylthioureas for enhanced asymmetric transfer hydrogenation of ketones ‒ experimental and theoretical studies
Catal. Sci. Technol., 2015, 5, 4790
1520740 CIFC20 H20 Cl2 N2 O2 Ru SP 21 21 216.503; 10.2867; 31.8305
90; 90; 90
2129.28Mary Sheeba, Mani; Preethi, Sankaranarayanan; Nijamudheen, A.; Muthu Tamizh, Manoharan; Datta, Ayan; Farrugia, Louis J.; Karvembu, Ramasamy
Half-sandwich Ru(η6-C6H6) complexes with chiral aroylthioureas for enhanced asymmetric transfer hydrogenation of ketones ‒ experimental and theoretical studies
Catal. Sci. Technol., 2015, 5, 4790
1520741 CIFC39 H69 Ga N2 Si3P -110.5026; 11.3327; 19.4036
85.025; 85.154; 71.124
2173.1Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520742 CIFC43 H80 Ga Li N2 Si4P 1 21/m 111.519; 20.858; 11.942
90; 117.73; 90
2539.7Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520743 CIFC47 H84 Ga Li N2 O2 Si3P 1 21/n 111.5267; 18.7832; 24.68
90; 90.988; 90
5342.6Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520744 CIFC43 H77 Ga N2 O Si3P -111.3181; 13.8704; 17.8645
69.483; 71.891; 67.251
2371.9Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520745 CIFC40 H71 Ga N2 Si3P 1 21/c 121.8907; 11.0318; 20.6366
90; 117.951; 90
4402.3Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520746 CIFC35 H58 N2 Si2 ZnC 1 2/c 110.6838; 19.4876; 18.4437
90; 102.692; 90
3746.18Uzelac, Marina; Hernán-Gómez, Alberto; Armstrong, David R.; Kennedy, Alan R.; Hevia, Eva
Rational synthesis of normal, abnormal and anionic NHC‒gallium alkyl complexes: structural, stability and isomerization insights
Chem. Sci., 2015, 6, 5719
1520747 CIFC42 H69 Al N2 Rh SiP 1 21/n 110.8994; 20.7161; 18.9857
90; 92.16; 90
4283.79Ekkert, Olga; White, Andrew J. P.; Toms, Harold; Crimmin, Mark R.
Addition of aluminium, zinc and magnesium hydrides to rhodium(iii)
Chem. Sci., 2015, 6, 5617
1520748 CIFC45 H73 N2 Rh Si ZnP -110.3195; 11.6531; 19.8109
77.86; 75.973; 73.269
2188Ekkert, Olga; White, Andrew J. P.; Toms, Harold; Crimmin, Mark R.
Addition of aluminium, zinc and magnesium hydrides to rhodium(iii)
Chem. Sci., 2015, 6, 5617
1520749 CIFC45 H73 Mg N2 Rh SiP -110.3775; 11.6602; 19.854
77.684; 75.691; 73.192
2202.2Ekkert, Olga; White, Andrew J. P.; Toms, Harold; Crimmin, Mark R.
Addition of aluminium, zinc and magnesium hydrides to rhodium(iii)
Chem. Sci., 2015, 6, 5617
1520750 CIFC72 H98 Al2 N4 Rh2C 1 2/c 117.4233; 16.5193; 23.4839
90; 104.958; 90
6530.1Ekkert, Olga; White, Andrew J. P.; Toms, Harold; Crimmin, Mark R.
Addition of aluminium, zinc and magnesium hydrides to rhodium(iii)
Chem. Sci., 2015, 6, 5617
1520751 CIFC22 H16 N2P 1 21/c 111.9993; 4.2453; 29.803
90; 100.261; 90
1493.9Suh, Sung-Eun; Barros, Stephanie A.; Chenoweth, David M.
Triple Aryne-Tetrazine Reaction Enabling Rapid Access to a New Class of Polyaromatic Heterocycles.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 5128-5132
1520752 CIFC20 H12 Cu2 N2 O10R -3 m :H18.7387; 18.7387; 37.4863
90; 90; 120
11399.4Li, Bin; Wen, Hui-Min; Wang, Hailong; Wu, Hui; Yildirim, Taner; Zhou, Wei; Chen, Banglin
Porous metal‒organic frameworks with Lewis basic nitrogen sites for high-capacity methane storage
Energy Environ. Sci., 2015, 8, 2504
1520753 CIFC13 H13 Cl N2 O2 SP 1 21/c 115.767; 5.759; 15.721
90; 112.32; 90
1320.5Lu, Lei; Ma, Juan; Qu, Panpan; Li, Feng
Effective Recognition of Different Types of Amino Groups: From Aminobenzenesulfonamides to Amino-(N-alkyl)benzenesulfonamides via Iridium-Catalyzed N-Alkylation with Alcohols.
Organic letters, 2015, 17, 2350-2353
1520754 CIFC23 H21 N O3 S2P -17.667; 8.7269; 17.0497
88.1161; 89.15; 62.1966
1008.54Miura, Tomoya; Funakoshi, Yuuta; Fujimoto, Yoshikazu; Nakahashi, Junki; Murakami, Masahiro
Facile synthesis of 2,5-disubstituted thiazoles from terminal alkynes, sulfonyl azides, and thionoesters.
Organic letters, 2015, 17, 2454-2457
1520755 CIFC270 H372 B6 N8 O30C 1 2/c 152.579; 21.835; 29.598
90; 117.54; 90
30130Danjo, Hiroshi; Kidena, Yuki; Kawahata, Masatoshi; Sato, Hiroyasu; Katagiri, Kosuke; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Multilayered inclusion nanocycles of anionic spiroborates.
Organic letters, 2015, 17, 2466-2469
1520756 CIFC28 H44 O4 Si2P 21 21 217.702; 13.1321; 27.4999
90; 90; 90
2781.4Shi, Hang; Tan, Ceheng; Zhang, Weibin; Zhang, Zichun; Long, Rong; Luo, Tuoping; Yang, Zhen
Synthetic Progress toward Azadirachtins. 1. Enantio- and Diastereoselective Synthesis of the Left-Wing Fragment of 11-epi-Azadirachtin I.
Organic letters, 2015, 17, 2342-2345
1520757 CIFC24 H20 O3P 1 21/c 117.7328; 8.7774; 13.0228
90; 110.419; 90
1899.61Li, Mingliang; Yang, Yudong; Zhou, Danni; Wan, Danyang; You, Jingsong
Nickel-Catalyzed Addition-Type Alkenylation of Unactivated, Aliphatic C-H Bonds with Alkynes: A Concise Route to Polysubstituted γ-Butyrolactones.
Organic letters, 2015, 17, 2546-2549
1520758 CIFC22 H33 N O9P -19.9044; 11.8847; 11.9608
60.57; 81.21; 75.803
1187.9Xu, Sanjia; Ciufolini, Marco A.
Formal Synthesis of (±)-Tetrodotoxin via the Oxidative Amidation of a Phenol: On the Structure of the Sato Lactone.
Organic letters, 2015, 17, 2424-2427
1520759 CIFC19 H27 N O10P -110.5221; 10.6666; 10.7161
74.105; 73.746; 61.845
1003.6Xu, Sanjia; Ciufolini, Marco A.
Formal Synthesis of (±)-Tetrodotoxin via the Oxidative Amidation of a Phenol: On the Structure of the Sato Lactone.
Organic letters, 2015, 17, 2424-2427
1520760 CIFC22 H36 O3P 21 21 218.1087; 11.9482; 20.232
90; 90; 90
1960.2Cheng, Shou-Ling; Jiang, Xiao-Ling; Shi, Yong; Tian, Wei-Sheng
Concise synthesis of the core structures of saundersiosides.
Organic letters, 2015, 17, 2346-2349
1520761 CIFC26 H40 O5P 21 21 217.3909; 12.9276; 25.254
90; 90; 90
2412.9Cheng, Shou-Ling; Jiang, Xiao-Ling; Shi, Yong; Tian, Wei-Sheng
Concise synthesis of the core structures of saundersiosides.
Organic letters, 2015, 17, 2346-2349
1520762 CIFC18 H23 N O4P 21 21 215.2667; 15.2534; 20.3019
90; 90; 90
1630.95Lin, Cheng-Wei; Hong, Bor-Cherng; Chang, Wan-Chen; Lee, Gene-Hsiang
A New Approach to Nitrones through Cascade Reaction of Nitro Compounds Enabled by Visible Light Photoredox Catalysis.
Organic letters, 2015, 17, 2314-2317
1520763 CIFC20 H30 Mo6 N4 Na4 O48 P4P -19.024; 19.4282; 21.1568
103.992; 95.5616; 103.407
3454.8Oms, Olivier; Benali, Tarik; Marrot, Jérome; Mialane, Pierre; Puget, Marin; Serier-Brault, Hélène; Deniard, Philippe; Dessapt, Rémi; Dolbecq, Anne
Fully Oxidized and Mixed-Valent Polyoxomolybdates Structured by Bisphosphonates with Pendant Pyridine Groups: Synthesis, Structure and Photochromic Properties
Inorganics, 2015, 3, 279
1520764 CIFC20 H30 K3.5 Mo6 N4 Na0.5 O45.5 P4P -117.9501; 19.4745; 19.8487
76.188; 69.59; 76.669
6231.6Oms, Olivier; Benali, Tarik; Marrot, Jérome; Mialane, Pierre; Puget, Marin; Serier-Brault, Hélène; Deniard, Philippe; Dessapt, Rémi; Dolbecq, Anne
Fully Oxidized and Mixed-Valent Polyoxomolybdates Structured by Bisphosphonates with Pendant Pyridine Groups: Synthesis, Structure and Photochromic Properties
Inorganics, 2015, 3, 279
1520765 CIFC32 H102.5 Mo8 N14 O53.25 P4P -117.6023; 22.134; 28.323
97.443; 95.464; 107.43
10334.2Oms, Olivier; Benali, Tarik; Marrot, Jérome; Mialane, Pierre; Puget, Marin; Serier-Brault, Hélène; Deniard, Philippe; Dessapt, Rémi; Dolbecq, Anne
Fully Oxidized and Mixed-Valent Polyoxomolybdates Structured by Bisphosphonates with Pendant Pyridine Groups: Synthesis, Structure and Photochromic Properties
Inorganics, 2015, 3, 279
1520766 CIFC2 H499 As8 Cs8.5 Na34.5 O538 W81 Y8P -121.7759; 32.0368; 33.0799
94.172; 107.537; 90.561
21934.4Ibrahim, Masooma; Bassil, Bassem; Kortz, Ulrich
Synthesis and Characterization of 8-Yttrium(III)-Containing 81-Tungsto-8-Arsenate(III), [Y8(CH3COO)(H2O)18(As2W19O68)4(W2O6)2(WO4)]43−
Inorganics, 2015, 3, 267
1520954 CIFC48 H64 Cl In N2 O2P -111.7715; 12.7462; 15.4167
105.421; 96.436; 103.43
2131.3Aluthge, D. C.; Ahn, J. M.; Mehrkhodavandi, P.
Overcoming aggregation in indium salen catalysts for isoselective lactide polymerization
Chem. Sci., 2015, 6, 5284
1520955 CIFC73 H103.5 In2 N8.5 O6P 21 21 2115.0752; 22.4148; 23.2893
90; 90; 90
7869.6Aluthge, D. C.; Ahn, J. M.; Mehrkhodavandi, P.
Overcoming aggregation in indium salen catalysts for isoselective lactide polymerization
Chem. Sci., 2015, 6, 5284
1520956 CIFC34 H46 Cl In N4 O2C 1 2 136.78; 8.3688; 24.188
90; 115.26; 90
6733.3Aluthge, D. C.; Ahn, J. M.; Mehrkhodavandi, P.
Overcoming aggregation in indium salen catalysts for isoselective lactide polymerization
Chem. Sci., 2015, 6, 5284
1520957 CIFC42 H58 In N3 O3P 21 21 219.192; 16.465; 25.858
90; 90; 90
3913.5Aluthge, D. C.; Ahn, J. M.; Mehrkhodavandi, P.
Overcoming aggregation in indium salen catalysts for isoselective lactide polymerization
Chem. Sci., 2015, 6, 5284
1520958 CIFC64 H58 In N3 O3 Si2P 21 21 2112.019; 20.066; 23.278
90; 90; 90
5614Aluthge, D. C.; Ahn, J. M.; Mehrkhodavandi, P.
Overcoming aggregation in indium salen catalysts for isoselective lactide polymerization
Chem. Sci., 2015, 6, 5284
1520959 CIFC25 H40 O2P 1 21 114.07; 10.406; 14.8885
90; 103.249; 90
2121.84Challinor, Victoria L.; Johnston, Ryne C.; Bernhardt, Paul V.; Lehmann, Reginald P.; Krenske, Elizabeth H.; De Voss, James J.
Biosynthetic insights provided by unusual sesterterpenes from the medicinal herb Aletris farinosa
Chem. Sci., 2015, 6, 5740
1520960 CIFC34 H30 Br N2 O5 P PdP 1 21 19.566; 10.649; 17.115
90; 95.18; 90
1736.4Xie, Lan-Gui; Bagutski, Viktor; Audisio, Davide; Wolf, Larry M.; Schmidts, Volker; Hofmann, Kathrin; Wirtz, Cornelia; Thiel, Walter; Thiele, Christina M.; Maulide, Nuno
Dynamic behaviour of monohaptoallylpalladium species: internal coordination as a driving force in allylic alkylation chemistry
Chem. Sci., 2015, 6, 5734
1520961 CIFC45 H27 B Cl8 F8 Ir N4P 1 21/n 19.2828; 22.6451; 24.351
90; 97.192; 90
5078.5Monti, Filippo; Baschieri, Andrea; Matteucci, Elia; Mazzanti, Andrea; Sambri, Letizia; Barbieri, Andrea; Armaroli, Nicola
A chelating diisocyanide ligand for cyclometalated Ir(iii) complexes with strong and tunable luminescence.
Faraday discussions, 2015, 185, 233-248
1521275 CIFC24 H43 Ir O2 P2P -18.5336; 11.7835; 13.3762
100.381; 95.958; 103.944
1268.7Rimoldi, M.; Fodor, D.; van Bokhoven, J. A.; Mezzetti, A.
Catalytic hydrogenation of liquid alkenes with a silica-grafted hydride pincer iridium(iii) complex: support for a heterogeneous mechanism
Catal. Sci. Technol., 2015, 5, 4575
1521276 CIFC25 H45 Ir O2 P2P 1 21/c 116.2181; 10.735; 15.8712
90; 107.894; 90
2629.5Rimoldi, M.; Fodor, D.; van Bokhoven, J. A.; Mezzetti, A.
Catalytic hydrogenation of liquid alkenes with a silica-grafted hydride pincer iridium(iii) complex: support for a heterogeneous mechanism
Catal. Sci. Technol., 2015, 5, 4575
1521277 CIFC20 H27 Br N4 OP 1 21 18.9698; 18.4284; 12.3981
90; 98.31; 90
2027.88Zaretsky, Serge; Hickey, Jennifer L.; Tan, Joanne; Pichugin, Dmitry; St. Denis, Megan A.; Ler, Spencer; Chung, Benjamin K. W.; Scully, Conor C. G.; Yudin, Andrei K.
Mechanistic investigation of aziridine aldehyde-driven peptide macrocyclization: the imidoanhydride pathway
Chem. Sci., 2015, 6, 5446
1521278 CIFC33 H53 N7 O7P 1 21 110.0804; 9.9982; 19.7575
90; 103.299; 90
1937.88Zaretsky, Serge; Hickey, Jennifer L.; Tan, Joanne; Pichugin, Dmitry; St. Denis, Megan A.; Ler, Spencer; Chung, Benjamin K. W.; Scully, Conor C. G.; Yudin, Andrei K.
Mechanistic investigation of aziridine aldehyde-driven peptide macrocyclization: the imidoanhydride pathway
Chem. Sci., 2015, 6, 5446
1521279 CIFC43 H72 Cl7 N P2 Pt RuP -19.6223; 14.2389; 18.6464
85.8029; 78.4958; 76.9593
2437.81Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521280 CIFC73 H96 Cl5 N P4 Pd RuP -111.5671; 13.5147; 24.091
76.202; 88.744; 72.724
3487.5Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521281 CIFC81 H144 Cl11 Ir O2 P4 Ru2C 1 2/c 113.811; 40.893; 16.343
90; 97.877; 90
9143Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521282 CIFC51 H92 Cl3 Ir P2 RuP -110.9458; 15.8362; 16.7533
111.788; 96.293; 99.958
2607.5Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521283 CIFC63 H88 As Cl7 O2 P2 Pt RuP -111.307; 13.305; 24.398
75.582; 88.059; 71.085
3358.5Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521284 CIFC46 H80 Cl5 P2 Rh RuP -110.935; 12.995; 18.693
78.174; 75.183; 75.241
2455.3Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521285 CIFC40 H74 Cl6 O P2 Pt Ru SP -110.432; 12.713; 19.025
77.214; 80.085; 82.926
2414.3Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521286 CIFC61 H83 Ag Cl8 F3 N3 O3 P2 Ru SP -113.297; 14.55; 18.906
111.639; 93.007; 92.517
3387.4Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521287 CIFC81.47 H144.4 Cl8.53 O3.16 P4 Rh2 Ru2C 1 2/c 132.65; 13.4; 23.89
90; 109.79; 90
9835Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521288 CIFC55 H79 Ag Cl8 F3 N3 O3 P2 Ru SP -114.248; 15.814; 16.607
70.503; 74.933; 68.534
3241.9Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521289 CIFC76 H134 Au B Cl10 F4 P4 Ru2P 1 2/c 119.988; 16.619; 27.233
90; 100.779; 90
8887Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1521290 CIFC37 H66 Au Cl3 P2 RuP 1 21/c 113.392; 17.683; 20.172
90; 121.735; 90
4062.7Reinholdt, Anders; Vibenholt, Johan E.; Morsing, Thorbjørn J.; Schau-Magnussen, Magnus; Reeler, Nini E. A.; Bendix, Jesper
Carbide complexes as π-acceptor ligands
Chem. Sci., 2015, 6, 5815
1523614 CIFC16 H13 N O4C 1 2/c 124.4884; 7.9625; 18.5286
90; 131.954; 90
2686.8Verma, Akhilesh K.; Danodia, Abhinandan K.; Saunthwal, Rakesh K.; Patel, Monika; Choudhary, Deepak
Palladium-Catalyzed Triple Successive C-H Functionalization: Direct Synthesis of Functionalized Carbazoles from Indoles.
Organic letters, 2015, 17, 3658-3661
1523944 CIFC32 H30 N2 O4 S4P -111.2966; 12.1022; 12.7036
85.244; 70.619; 77.661
1600.36Yadagiri, Dongari; Anbarasan, Pazhamalai
Tandem 1,2-sulfur migration and (aza)-Diels‒Alder reaction of β-thio-α-diazoimines: rhodium catalyzed synthesis of (fused)-polyhydropyridines, and cyclohexenes
Chem. Sci., 2015, 6, 5847
1523945 CIFC24 H40 N4 O4 SiP n a 2118.1083; 17.6737; 7.671
90; 90; 90
2455.03Kaßner, L.; Nagel, K.; Grützner, R.-E.; Korb, M.; Rüffer, T.; Lang, H.; Spange, S.
Polyamide 6/silica hybrid materials by a coupled polymerization reaction
Polym. Chem., 2015, 6, 6297
1523946 CIFC24 H40 N4 O4 SiI -4 2 d13.9688; 13.9688; 13.3347
90; 90; 90
2601.96Kaßner, L.; Nagel, K.; Grützner, R.-E.; Korb, M.; Rüffer, T.; Lang, H.; Spange, S.
Polyamide 6/silica hybrid materials by a coupled polymerization reaction
Polym. Chem., 2015, 6, 6297
1529061 CIFC37 H22 B F9P -110.1241; 10.1353; 17.3058
84.1092; 73.833; 63.9157
1531.42Zhang, Zuolun; Edkins, Robert M.; Haehnel, Martin; Wehner, Marius; Eichhorn, Antonius; Mailänder, Lisa; Meier, Michael; Brand, Johannes; Brede, Franziska; Müller-Buschbaum, Klaus; Braunschweig, Holger; Marder, Todd B.
Taming the beast: fluoromesityl groups induce a dramatic stability enhancement in boroles
Chem. Sci., 2015, 6, 5922
1529062 CIFC28 H18 B F9P -19.7736; 16.1049; 16.4046
76.766; 74.775; 75.51
2375.1Zhang, Zuolun; Edkins, Robert M.; Haehnel, Martin; Wehner, Marius; Eichhorn, Antonius; Mailänder, Lisa; Meier, Michael; Brand, Johannes; Brede, Franziska; Müller-Buschbaum, Klaus; Braunschweig, Holger; Marder, Todd B.
Taming the beast: fluoromesityl groups induce a dramatic stability enhancement in boroles
Chem. Sci., 2015, 6, 5922
1529063 CIFC28 H20 B F9 OP 1 21/n 18.6666; 35.693; 15.69
90; 91.689; 90
4851.4Zhang, Zuolun; Edkins, Robert M.; Haehnel, Martin; Wehner, Marius; Eichhorn, Antonius; Mailänder, Lisa; Meier, Michael; Brand, Johannes; Brede, Franziska; Müller-Buschbaum, Klaus; Braunschweig, Holger; Marder, Todd B.
Taming the beast: fluoromesityl groups induce a dramatic stability enhancement in boroles
Chem. Sci., 2015, 6, 5922
1529064 CIFC37 H56 N8 O9P 1 21 19.2715; 36.7577; 11.3129
90; 90.098; 90
3855.4Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Dibonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis
Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability
Chem. Sci., 2015, 6, 5473
1529065 CIFC40 H68 N8 O13P 1 21 113.3658; 9.4864; 17.7634
90; 104.204; 90
2183.42Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Dibonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis
Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability
Chem. Sci., 2015, 6, 5473
1529066 CIFC36 H52 N8 O9I 1 2 116.9971; 9.2681; 25.8496
90; 99.408; 90
4017.3Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Dibonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis
Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability
Chem. Sci., 2015, 6, 5473
1529067 CIFC39 H64 N8 O12P 1 21 117.7309; 9.6245; 26.236
90; 107.755; 90
4263.9Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Dibonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis
Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability
Chem. Sci., 2015, 6, 5473
1529068 CIFC39 H64 N8 O12P 1 21 19.769; 13.318; 17.543
90; 103.191; 90
2222.2Bartoloni, Marco; Jin, Xian; Marcaida, Maria José; Banha, João; Dibonaventura, Ivan; Bongoni, Swathi; Bartho, Kathrin; Gräbner, Olivia; Sefkow, Michael; Darbre, Tamis; Reymond, Jean-Louis
Bridged bicyclic peptides as potential drug scaffolds: synthesis, structure, protein binding and stability
Chem. Sci., 2015, 6, 5473
1529074 CIFC18 H18 F2 N O4 VP 1 21/n 117.7691; 7.9596; 25.4492
90; 107.241; 90
3437.67Choing, Stephanie N.; Francis, Aaron J.; Clendenning, Graham; Schuurman, Michael S.; Sommer, Roger D.; Tamblyn, Isaac; Weare, Walter W.; Cuk, Tanja
Long-Lived LMCT in a d0Vanadium(V) Complex by Internal Conversion to a State of 3dxyCharacter
The Journal of Physical Chemistry C, 2015, 119, 17029
1529075 CIFC28.52 H21.52 F6 N0.48 O2 S2P 1 21/c 118.2529; 6.5741; 21.2658
90; 100.998; 90
2504.95Ohshima, Satoko; Morimoto, Masakazu; Irie, Masahiro
Light-driven bending of diarylethene mixed crystals
Chem. Sci., 2015, 6, 5746
1529076 CIFC27 H20 F6 N2 O2 S2P -115.141; 18.267; 19.761
72.453; 86.674; 77.582
5089Ohshima, Satoko; Morimoto, Masakazu; Irie, Masahiro
Light-driven bending of diarylethene mixed crystals
Chem. Sci., 2015, 6, 5746
1529077 CIFC113.3 H88.95 Cl2 Cu2 F24 N15.65 O14 S2P 32 2 129.93; 29.93; 28.878
90; 90; 120
22403Mortezaei, Shahab; Catarineu, Noelle R.; Duan, Xueyou; Hu, Chunhua; Canary, James W.
Redox-configurable ambidextrous catalysis: structural and mechanistic insight
Chem. Sci., 2015, 6, 5904
1529078 CIFC65.36 H70.72 N4 O2.68C 1 2/c 134.794; 5.836; 28.131
90; 97.862; 90
5659Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529079 CIFC66 H67 N4 O2C 1 2/c 134.89; 5.8074; 28.103
90; 98.31; 90
5634.4Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529080 CIFC68 H71 N4 O4.5C 1 2/c 134.814; 5.8498; 27.956
90; 98.517; 90
5630.6Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529081 CIFC63 H69 N4 O3C 1 2/c 134.994; 5.7712; 28.005
90; 97.696; 90
5604.9Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529082 CIFC63 H69 N7 O6C 1 2/c 134.875; 5.794; 28.028
90; 98.453; 90
5602Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529083 CIFC68 H68 N4 O2C 1 2/c 135.119; 5.8515; 28.129
90; 96.944; 90
5738Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529084 CIFC68 H70 N4P -15.8032; 17.6171; 28.095
82.852; 89.95; 81.848
2820.8Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529085 CIFC70 H76 N4C 1 2 134.833; 5.8219; 28.205
90; 98.49; 90
5657.1Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529086 CIFC74 H72 N4P -15.8111; 17.553; 28.328
82.08; 89.417; 83.086
2841.1Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529087 CIFC70 H74 N6C 1 2 135.689; 5.9481; 28.84
90; 97.562; 90
6069Sanna, Elena; Escudero-Adán, Eduardo C.; Bauzá, Antonio; Ballester, Pablo; Frontera, Antonio; Rotger, Carmen; Costa, Antonio
A crystalline sponge based on dispersive forces suitable for X-ray structure determination of included molecular guests
Chem. Sci., 2015, 6, 5466
1529088 CIFC133 H99 Cu5.5 N17 O31R -3 :H29.5994; 29.5994; 52.255
90; 90; 120
39648Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529089 CIFC168 H156 Cu3 F0 N12 O27 S0C 1 2/c 157.029; 34.131; 24.4704
90; 95.496; 90
47412Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529090 CIFC128 H126 Br4 Cu2 N6 O17 S4P 1 21/n 111.0753; 32.119; 47.079
90; 92.659; 90
16729Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529091 CIFC108 H102 Cu2 F12 N10 O36 S4P -114.4856; 18.0721; 30.4166
96.787; 93.193; 102.088
7704.9Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529092 CIFC47 H44.5 B Cu F4 N5.5 O11P b c a9.459; 29.785; 34.465
90; 90; 90
9710Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529093 CIFC149 H187 B4 Cu2 F16 N19 O34.5P 1 21/c 128.9123; 20.7706; 29.7284
90; 101.224; 90
17511.2Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529094 CIFC93 H105 Br3 Cu2 N6 O16.5 S4.5P -115.4223; 19.5085; 28.1607
100.656; 105.671; 102.75
7682Thorp-Greenwood, Flora L.; Ronson, Tanya K.; Hardie, Michaele J.
Copper coordination polymers from cavitand ligands: hierarchical spaces from cage and capsule motifs, and other topologies
Chem. Sci., 2015, 6, 5779
1529193 CIFC23 H20 Br N O2P -19.823; 10.177; 11.186
92.48; 113.89; 100.8
995.5Sha, Qiang; Arman, Hadi; Doyle, Michael P.
Three-Component Cascade Reactions with 2,3-Diketoesters: A Novel Metal-Free Synthesis of 5-Vinyl-pyrrole and 4-Hydroxy-indole Derivatives.
Organic letters, 2015, 17, 3876-3879
1529194 CIFC94 H120 N6 O2 Y2P 1 21/n 113.16; 16.367; 19.701
90; 103.837; 90
4120Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529195 CIFC98 H128 N6 O2 Y2P 1 21/n 113.324; 16.849; 19.59
90; 104.35; 90
4261Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529196 CIFC98 H128 N6 O4 Y2P 1 21/n 113.2137; 17.8164; 18.8346
90; 102.372; 90
4331.1Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529197 CIFC70 H100 N6 O2 Y2C 1 2/c 116.313; 20.362; 20.231
90; 92.019; 90
6716Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529198 CIFC94 H120 N6 O2 Y2P 1 21/n 115.639; 17.514; 16.24
90; 104.711; 90
4302Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529199 CIFC72 H104 N6 O4 Y2P 1 21/n 113.492; 13.673; 19.028
90; 101.334; 90
3442Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529200 CIFC47 H62 N3 O2 YP 1 21/n 112.902; 21.925; 16.088
90; 106.222; 90
4370Shibata, Yu; Nagae, Haruki; Sumiya, Shiki; Rochat, Raphaël; Tsurugi, Hayato; Mashima, Kazushi
2,2′-Bipyridyl formation from 2-arylpyridines through bimetallic diyttrium intermediate
Chem. Sci., 2015, 6, 5394
1529201 CIFC71.5 H54 Al Cl5 N4 O3P 1 21/c 115.72; 14.2236; 28.919
90; 96.12; 90
6429.3Gao, Bo; Li, Dongni; Li, Xiang; Duan, Ranlong; Pang, Xuan; Cui, Yuan; Duan, Qian; Chen, Xuesi
Preparation of biocompatible, biodegradable and sustainable polylactides catalyzed by aluminum complexes bearing unsymmetrical dinaphthalene-imine derivatives via ring-opening polymerization of lactides
Catal. Sci. Technol., 2015, 5, 4644
1529202 CIFC68 H50 Al Cl3 N4 O2P 1 21/n 114.265; 20.847; 18.412
90; 97.691; 90
5426.2Gao, Bo; Li, Dongni; Li, Xiang; Duan, Ranlong; Pang, Xuan; Cui, Yuan; Duan, Qian; Chen, Xuesi
Preparation of biocompatible, biodegradable and sustainable polylactides catalyzed by aluminum complexes bearing unsymmetrical dinaphthalene-imine derivatives via ring-opening polymerization of lactides
Catal. Sci. Technol., 2015, 5, 4644
1529203 CIFC43.5 H73 N6 O P Si6 UP -111.5703; 11.7055; 21.152
86.747; 83.81; 75.03
2750.1Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529204 CIFC40 H69 N6 O P Si6 ThP -111.4301; 21.3302; 24.614
99.881; 90.073; 95.606
5882.8Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529205 CIFC40 H69 N7 O Si6 UC 1 2/c 115.5201; 17.9868; 37.3806
90; 97.783; 90
10338.9Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529206 CIFC43.5 H73 N7 O Si6 ThP -111.2966; 23.057; 23.27
66.405; 87.39; 77.614
5419.5Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529207 CIFC43.5 H73 N7 S Si6 UP -111.581; 11.6278; 21.115
86.775; 83.982; 75.259
2733.3Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529208 CIFC43.5 H73 N7 S Si6 ThP -111.6047; 11.6602; 21.204
86.479; 83.836; 75.464
2759.5Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529209 CIFC52.5 H91.5 N6 Ni O P Si6 ThP -114.8598; 19.6824; 24.2681
105.87; 101.321; 96.5472
6587.8Camp, Clément; Settineri, Nicholas; Lefèvre, Julia; Jupp, Andrew R.; Goicoechea, José M.; Maron, Laurent; Arnold, John
Uranium and thorium complexes of the phosphaethynolate ion
Chem. Sci., 2015, 6, 6379
1529210 CIFC114 H143 Cl N14 O5P 1 21/n 110.9481; 39.559; 24.446
90; 92.404; 90
10578Galán, Albano; Valderrey, Virginia; Ballester, Pablo
Ordered co-encapsulation of chloride with polar neutral guests in a tetraurea calix[4]pyrrole dimeric capsule
Chem. Sci., 2015, 6, 6325
1529211 CIFC16 H11 N O2P 1 21/c 115.281; 3.8302; 24.754
90; 125.705; 90
1176.5Karad, Somnath Narayan; Chung, Wei-Kang; Liu, Rai-Shung
Gold-catalyzed formal [4π + 2π]-cycloadditions of propiolate derivatives with unactivated nitriles
Chem. Sci., 2015, 6, 5964
1529212 CIFC16 H12 O3P 1 21/n 16.0914; 8.5177; 23.947
90; 90.598; 90
1242.4Karad, Somnath Narayan; Chung, Wei-Kang; Liu, Rai-Shung
Gold-catalyzed formal [4π + 2π]-cycloadditions of propiolate derivatives with unactivated nitriles
Chem. Sci., 2015, 6, 5964
1529213 CIFC18 H16 O3P 1 21 17.946; 9.4371; 9.6309
90; 100.506; 90
710.09Karad, Somnath Narayan; Chung, Wei-Kang; Liu, Rai-Shung
Gold-catalyzed formal [4π + 2π]-cycloadditions of propiolate derivatives with unactivated nitriles
Chem. Sci., 2015, 6, 5964
1529214 CIFC92 H76 Dy N11 OP 1 21/c 117.5705; 22.6256; 24.6091
90; 100.073; 90
9632.4Cao, Wei; Gao, Chen; Zhang, Yi-Quan; Qi, Dongdong; Liu, Tao; Wang, Kang; Duan, Chunying; Gao, Song; Jiang, Jianzhuang
Rational enhancement of the energy barrier of bis(tetrapyrrole) dysprosium SMMs via replacing atom of porphyrin core
Chem. Sci., 2015, 6, 5947
1529215 CIFC189 H157 Cl15 Dy2 N22 S2C 1 2/c 131.8037; 17.264; 32.0054
90; 102.045; 90
17186Cao, Wei; Gao, Chen; Zhang, Yi-Quan; Qi, Dongdong; Liu, Tao; Wang, Kang; Duan, Chunying; Gao, Song; Jiang, Jianzhuang
Rational enhancement of the energy barrier of bis(tetrapyrrole) dysprosium SMMs via replacing atom of porphyrin core
Chem. Sci., 2015, 6, 5947
1529216 CIFC26 H21 Cl N2 O2P 21 21 219.5286; 10.2653; 21.7873
90; 90; 90
2131.1Li, Bao-Sheng; Wang, Yuhuang; Jin, Zhichao; Chi, Yonggui Robin
Cycloaddition of cyclobutenone and azomethine imine enabled by chiral isothiourea organic catalysts
Chem. Sci., 2015, 6, 6008
1529231 CIF
HKL
C8 H11 K N2 O2 SP 21 21 214.2541; 14.739; 16.635
90; 90; 90
1043Golovnev, Nikolay; Molokeev, Maxim; Vereshchagin, Sergey; Sterkhova, Irina; Atuchin, Victor
The cis-trans isomer transformation, spectroscopic and thermal properties of Li, Na, K 1,3-diethyl-2-thiobarbiturate complexes
Polyhedron, 2015, 85, 493
1529232 CIF
HKL
C8 H11 N2 Na O2 SP 1 21/n 110.5339; 7.6036; 14.186
90; 108.964; 90
1074.6Golovnev, Nikolay; Molokeev, Maxim; Vereshchagin, Sergey; Sterkhova, Irina; Atuchin, Victor
The cis-trans isomer transformation, spectroscopic and thermal properties of Li, Na, K 1,3-diethyl-2-thiobarbiturate complexes
Polyhedron, 2015, 85, 493
1529233 CIF
HKL
C8 H11 Li N2 O2 SP 1 21/n 110.6778; 7.2687; 13.2021
90; 108.841; 90
969.8Golovnev, Nikolay; Molokeev, Maxim; Vereshchagin, Sergey; Sterkhova, Irina; Atuchin, Victor
The cis-trans isomer transformation, spectroscopic and thermal properties of Li, Na, K 1,3-diethyl-2-thiobarbiturate complexes
Polyhedron, 2015, 85, 493
1529234 CIF
HKL
C10 H17 N4 Nd O10 S2P 1 21/n 18.5939; 22.9953; 10.1832
90; 112.838; 90
1854.64Golovnev, Nikolay; Molokeev, Maxim; Vereshchagin, Sergey; Atuchin, Victor
Synthesis and thermal transformation of a neodymium(III) complex [Nd(HTBA)2(C2H3O2)(H2O)2].2H2O to noncentrosymmetric oxosulfate Nd2O2SO4
Journal of Coordination Chemistry, 2015, 68, 1865
1529235 CIF
HKL
Nd2 O6 SI 2 2 24.11991; 4.22332; 13.349
90; 90; 90
232.27Golovnev, Nikolay; Molokeev, Maxim; Vereshchagin, Sergey; Atuchin, Victor
Synthesis and thermal transformation of a neodymium(III) complex [Nd(HTBA)2(C2H3O2)(H2O)2].2H2O to noncentrosymmetric oxosulfate Nd2O2SO4
Journal of Coordination Chemistry, 2015, 68, 1865
1529237 CIF
HKL
C16 H22 N4 O4 Pb S2R -3 :H12.9503; 12.9503; 32.0771
90; 90; 120
4658.9Golovnev, Nikolay; Molokeev, Maxim; Golovneva, Irina
The crystal structure of lead(II) 1,3-diethyl-2-thiobarbiturate
Russian Journal of Coordination Chemistry, 2015, 41, 300
1529239 CIF
HKL
C8 H11 Cs N2 O2 SP 21 21 214.5236; 14.739; 16.937
90; 90; 90
1129.2Molokeev, Maxim; Golovnev, Nikolay; Vereshchagin, Sergey; Atuchin, Victor
Crystal structure, spectroscopic and thermal properties of the 1,3-diethyl-2-thiobarbiturate of Rb+, Cs+, Tl+ and NH4+ complexes
Polyhedron, 2015, 98, 113
1529240 CIF
HKL
C8 H15 N3 O2 SP -18.472; 8.853; 8.964
98.436; 116.059; 109.916
531.8Molokeev, Maxim; Golovnev, Nikolay; Vereshchagin, Sergey; Atuchin, Victor
Crystal structure, spectroscopic and thermal properties of the 1,3-diethyl-2-thiobarbiturate of Rb+, Cs+, Tl+ and NH4+ complexes
Polyhedron, 2015, 98, 113
1529241 CIF
HKL
C8 H11 N2 O2 Rb SP 21 21 214.373; 14.789; 16.923
90; 90; 90
1094.4Molokeev, Maxim; Golovnev, Nikolay; Vereshchagin, Sergey; Atuchin, Victor
Crystal structure, spectroscopic and thermal properties of the 1,3-diethyl-2-thiobarbiturate of Rb+, Cs+, Tl+ and NH4+ complexes
Polyhedron, 2015, 98, 113
1529242 CIF
HKL
C8 H11 N2 O2 S TlP 21 21 214.3767; 14.7003; 16.6064
90; 90; 90
1068.44Molokeev, Maxim; Golovnev, Nikolay; Vereshchagin, Sergey; Atuchin, Victor
Crystal structure, spectroscopic and thermal properties of the 1,3-diethyl-2-thiobarbiturate of Rb+, Cs+, Tl+ and NH4+ complexes
Polyhedron, 2015, 98, 113
1529249 CIFC13 H18 N2 O4P 1 21/n 19.4119; 7.6136; 18.3824
90; 104.166; 90
1277.2Diaba, Faïza; Montiel, Juan A.; Serban, Georgeta; Bonjoch, Josep
Synthesis of Normorphans through an Efficient Intramolecular Carbamoylation of Ketones.
Organic letters, 2015, 17, 3860-3863
1529250 CIFC16 H16 Cl N O2P n a 217.9657; 14.5166; 12.0126
90; 90; 90
1389.08Diaba, Faïza; Montiel, Juan A.; Serban, Georgeta; Bonjoch, Josep
Synthesis of Normorphans through an Efficient Intramolecular Carbamoylation of Ketones.
Organic letters, 2015, 17, 3860-3863
1529251 CIFC42 H3 B F32 N3 PP -110.7013; 11.2094; 17.8097
90.007; 104.509; 98.16
2045.87Winkelhaus, Daniel; Holthausen, Michael H.; Dobrovetsky, Roman; Stephan, Douglas W.
Phosphine and carbene azido-cations: [(L)N3]+and [(L)2N3]+
Chem. Sci., 2015, 6, 6367
1529252 CIFC60 H30 B F20 N3 P2P 1 21/n 112.8405; 18.5144; 22.501
90; 90.649; 90
5348.9Winkelhaus, Daniel; Holthausen, Michael H.; Dobrovetsky, Roman; Stephan, Douglas W.
Phosphine and carbene azido-cations: [(L)N3]+and [(L)2N3]+
Chem. Sci., 2015, 6, 6367
1529253 CIFC48 H54 B F20 N3 P2P -112.7734; 14.9217; 15.1042
107.504; 95.932; 111.054
2489Winkelhaus, Daniel; Holthausen, Michael H.; Dobrovetsky, Roman; Stephan, Douglas W.
Phosphine and carbene azido-cations: [(L)N3]+and [(L)2N3]+
Chem. Sci., 2015, 6, 6367
1529254 CIFC42 H50 B Cl0 F2 N7P -111.7044; 16.5009; 18.3335
86.77; 76.082; 83.169
3411Winkelhaus, Daniel; Holthausen, Michael H.; Dobrovetsky, Roman; Stephan, Douglas W.
Phosphine and carbene azido-cations: [(L)N3]+and [(L)2N3]+
Chem. Sci., 2015, 6, 6367
1529255 CIFC42 H15 B F20 N3 PP 1 21/n 112.226; 23.2442; 14.116
90; 107.089; 90
3834.42Winkelhaus, Daniel; Holthausen, Michael H.; Dobrovetsky, Roman; Stephan, Douglas W.
Phosphine and carbene azido-cations: [(L)N3]+and [(L)2N3]+
Chem. Sci., 2015, 6, 6367
1529256 CIFC27 H42 O11P 21 21 2110.5266; 14.2874; 18.9078
90; 90; 90
2843.69Jin, An; Wu, Wen-Ming; Yu, Heng-Yi; Zhou, Ming; Liu, Ye; Tian, Tian; Ruan, Han-Li
Bisabolane-Type Sesquiterpenoids from the Whole Plant of Parasenecio rubescens.
Journal of natural products, 2015, 78, 2057-2066
1529257 CIFC19 H20 N2 O5 SP 1 21 111.1369; 12.7954; 13.7775
90; 105.869; 90
1888.49Feng, Huan-Xi; Tan, Rui; Liu, Yan-Kai
An Efficient One-Pot Approach to the Construction of Chiral Nitrogen-Containing Heterocycles under Mild Conditions.
Organic letters, 2015, 17, 3794-3797
1529258 CIFC19.5 H15 N4 O0.5P 1 21/c 111.4678; 19.447; 15.154
90; 112.202; 90
3129He, Liang; Li, Yi; Tan, Cai-Ping; Ye, Rui-Rong; Chen, Mu-He; Cao, Jian-Jun; Ji, Liang-Nian; Mao, Zong-Wan
Cyclometalated iridium(iii) complexes as lysosome-targeted photodynamic anticancer and real-time tracking agents
Chem. Sci., 2015, 6, 5409
1529259 CIFC44 H36 F10 Ir N6 O2 PP -18.5758; 14.436; 17.199
79.43; 89.672; 84.686
2084He, Liang; Li, Yi; Tan, Cai-Ping; Ye, Rui-Rong; Chen, Mu-He; Cao, Jian-Jun; Ji, Liang-Nian; Mao, Zong-Wan
Cyclometalated iridium(iii) complexes as lysosome-targeted photodynamic anticancer and real-time tracking agents
Chem. Sci., 2015, 6, 5409
1529260 CIFC17 H18 O3P -16.2616; 9.355; 11.752
87.526; 88.241; 86.453
686.17Dange, Nitin S.; Stepherson, Jacob R.; Ayala, Caitlan E.; Fronczek, Frank R.; Kartika, Rendy
Cooperative benzylic‒oxyallylic stabilized cations: regioselective construction of α-quaternary centers in ketone-derived compounds
Chem. Sci., 2015, 6, 6312
1529261 CIFC20 H19 N OR -3 :H25.0795; 25.0795; 13.9752
90; 90; 120
7612.5Dange, Nitin S.; Stepherson, Jacob R.; Ayala, Caitlan E.; Fronczek, Frank R.; Kartika, Rendy
Cooperative benzylic‒oxyallylic stabilized cations: regioselective construction of α-quaternary centers in ketone-derived compounds
Chem. Sci., 2015, 6, 6312
1529262 CIFC22 H23 N O2P 1 21/c 114.0542; 15.9871; 7.7187
90; 91.974; 90
1733.25Dange, Nitin S.; Stepherson, Jacob R.; Ayala, Caitlan E.; Fronczek, Frank R.; Kartika, Rendy
Cooperative benzylic‒oxyallylic stabilized cations: regioselective construction of α-quaternary centers in ketone-derived compounds
Chem. Sci., 2015, 6, 6312
1529263 CIFC23 H25 N O2P b c a7.5352; 16.1007; 30.3669
90; 90; 90
3684.2Dange, Nitin S.; Stepherson, Jacob R.; Ayala, Caitlan E.; Fronczek, Frank R.; Kartika, Rendy
Cooperative benzylic‒oxyallylic stabilized cations: regioselective construction of α-quaternary centers in ketone-derived compounds
Chem. Sci., 2015, 6, 6312
1529264 CIFC23 H23 N O3P 21 21 217.2261; 13.4245; 18.999
90; 90; 90
1843.03Dange, Nitin S.; Stepherson, Jacob R.; Ayala, Caitlan E.; Fronczek, Frank R.; Kartika, Rendy
Cooperative benzylic‒oxyallylic stabilized cations: regioselective construction of α-quaternary centers in ketone-derived compounds
Chem. Sci., 2015, 6, 6312
1529265 CIFC21 H23 N OP -112.0196; 12.4522; 14.0202
94.894; 114.29; 113.544
1673.4Dange, Nitin S.; Stepherson, Jacob R.; Ayala, Caitlan E.; Fronczek, Frank R.; Kartika, Rendy
Cooperative benzylic‒oxyallylic stabilized cations: regioselective construction of α-quaternary centers in ketone-derived compounds
Chem. Sci., 2015, 6, 6312
1529271 CIF
HKL
B4 Mn5.64 Ni6.36 O20P b a m9.1757; 12.3163; 2.9978
90; 90; 90
338.78Bezmaternykh, Leonard; Kolesnikova, Evgeniya; Eremin, Evgeniy; Seryotkin, Yuriy; Molokeev, Maxim; Volkov, Nikita
Spin-lattice coupling and peculiarities of magnetic behavior of ferrimagnetic ludwigites Mn0.5(2+)M1.5(2+)Mn(3+)BO5 (M=Cu, Ni)
Solid State Phenomena, 2015, 233, 133
1529272 CIF
HKL
F6.82 N3 SnP m -3 m6.092385; 6.092385; 6.092385
90; 90; 90
226.132Flerov, Igor; Molokeev, Maxim; Laptash, Natalia; Udovenko, Anatoly; Pogoreltsev, Evgeniy; Melnikova, Svetlana; Misyul, Sergey
Structural transformation between two cubic phases of (NH4)3SnF7
Journal of Fluorine Chemistry, 2015, 179, 86
1529273 CIF
HKL
F7 H12 N3 SnP a -312.0866; 12.0866; 12.0866
90; 90; 90
1765.68Flerov, Igor; Molokeev, Maxim; Laptash, Natalia; Udovenko, Anatoly; Pogoreltsev, Evgeniy; Melnikova, Svetlana; Misyul, Sergey
Structural transformation between two cubic phases of (NH4)3SnF7
Journal of Fluorine Chemistry, 2015, 179, 86
1529274 CIF
HKL
Ca Gd2 O16 W4C 1 2/c 17.33924; 11.4246; 5.22523
90; 134.368; 90
313.2Lim, Chang Sung; Aleksandrovsky, Aleksandr; Molokeev, Maxim; Oreshonkov, Alexandr; Atuchin, Victor
Microwave sol-gel synthesis and upconversion photoluminescence properties of CaGd2(WO4)4_Er3+Yb3+ phosphors with incommensurately modulated structure
Journal of Solid State Chemistry, 2015, 228, 160
1529275 CIF
HKL
Ca Er0.2 Gd1.8 O16 W4C 1 2/c 17.32393; 11.41202; 5.21863
90; 134.279; 90
312.28Lim, Chang Sung; Aleksandrovsky, Aleksandr; Molokeev, Maxim; Oreshonkov, Alexandr; Atuchin, Victor
Microwave sol-gel synthesis and upconversion photoluminescence properties of CaGd2(WO4)4:Er3+/Yb3+ phosphors with incommensurately modulated structure
Journal of Solid State Chemistry, 2015, 228, 160
1529276 CIF
HKL
Ca Er0.1 Gd1.7 O16 W4 Yb0.2C 1 2/c 17.29238; 11.39539; 5.20988
90; 134.098; 90
310.91Lim, Chang Sung; Aleksandrovsky, Aleksandr; Molokeev, Maxim; Oreshonkov, Alexandr; Atuchin, Victor
Microwave sol-gel synthesis and upconversion photoluminescence properties of CaGd2(WO4)4:Er3+/Yb3+ phosphors with incommensurately modulated structure
Journal of Solid State Chemistry, 2015, 228, 160
1529277 CIF
HKL
Ca Er0.05 Gd1.5 O16 W4 Yb0.45C 1 2/c 17.31297; 11.38508; 5.20846
90; 134.325; 90
310.23Lim, Chang Sung; Aleksandrovsky, Aleksandr; Molokeev, Maxim; Oreshonkov, Alexandr; Atuchin, Victor
Microwave sol-gel synthesis and upconversion photoluminescence properties of CaGd2(WO4)4_Er3+Yb3+ phosphors with incommensurately modulated structure
Journal of Solid State Chemistry, 2015, 228, 160
1529278 CIFC10 H10 Br2 O6P -16.911; 7.727; 12.082
101.66; 97.22; 106.59
593.91Itoh, Takahito; Nomura, Shinji; Nakasho, Hirofumi; Uno, Takahiro; Kubo, Masataka; Tohnai, Norimitsu; Miyata, Mikiji
Halogen Bond Effect for Single-Crystal-to-Single-Crystal Transformation: Topochemical Polymerization of Substituted Quinodimethane
Macromolecules, 2015, 48, 5450
1529279 CIFC10 H10 Br2 O4P -16.795; 8.051; 11.928
98.28; 103.43; 106.3
593.7Itoh, Takahito; Nomura, Shinji; Nakasho, Hirofumi; Uno, Takahiro; Kubo, Masataka; Tohnai, Norimitsu; Miyata, Mikiji
Halogen Bond Effect for Single-Crystal-to-Single-Crystal Transformation: Topochemical Polymerization of Substituted Quinodimethane
Macromolecules, 2015, 48, 5450
1529280 CIFC17 H13 NP 1 21/c 18.8383; 21.101; 6.6024
90; 91.311; 90
1231Mandal, Sumana; Mahato, Sujit; Jana, Chandan K.
Direct β-C(sp(3))-H Functionalization of Aliphatic Amines to α,β-Unsaturated Imines, Aldehydes, and Chromenes.
Organic letters, 2015, 17, 3762-3765
1529281 CIFC24 H21 N O4 SP 1 21/c 117.7457; 5.8725; 20.1502
90; 103.189; 90
2044.5Kuppusamy, Ramajayam; Gandeepan, Parthasarathy; Cheng, Chien-Hong
Rh(III)-Catalyzed [4 + 1] Annulations of 2-Hydroxy- and 2-Aminobenzaldehydes with Allenes: A Simple Method toward 3-Coumaranones and 3-Indolinones.
Organic letters, 2015, 17, 3846-3849
1529282 CIFC17 H13 Br O2P n a 2129.2958; 6.1415; 15.5413
90; 90; 90
2796.2Kuppusamy, Ramajayam; Gandeepan, Parthasarathy; Cheng, Chien-Hong
Rh(III)-Catalyzed [4 + 1] Annulations of 2-Hydroxy- and 2-Aminobenzaldehydes with Allenes: A Simple Method toward 3-Coumaranones and 3-Indolinones.
Organic letters, 2015, 17, 3846-3849
1529283 CIFC18 H27 N O4P 21 21 2110.1466; 10.1835; 16.6612
90; 90; 90
1721.57Lin, Kuo-Wei; Ananthan, Bakthavachalam; Tseng, Sheng-Fang; Yan, Tu-Hsin
Exceedingly Concise and Elegant Synthesis of (+)-Paniculatine, (-)-Magellanine, and (+)-Magellaninone.
Organic letters, 2015, 17, 3938-3940
1529284 CIFC17 H27 N O2P 1 21 18.2578; 7.6701; 12.4589
90; 99.389; 90
778.55Lin, Kuo-Wei; Ananthan, Bakthavachalam; Tseng, Sheng-Fang; Yan, Tu-Hsin
Exceedingly Concise and Elegant Synthesis of (+)-Paniculatine, (-)-Magellanine, and (+)-Magellaninone.
Organic letters, 2015, 17, 3938-3940
1529285 CIFC18 H25 N O4P 1 21 18.5383; 7.6057; 12.8523
90; 104.589; 90
807.71Lin, Kuo-Wei; Ananthan, Bakthavachalam; Tseng, Sheng-Fang; Yan, Tu-Hsin
Exceedingly Concise and Elegant Synthesis of (+)-Paniculatine, (-)-Magellanine, and (+)-Magellaninone.
Organic letters, 2015, 17, 3938-3940
1529286 CIFC60 H64 O6 P2P -111.135; 11.644; 12.132
97.161; 111.866; 112.432
1282.5Yamamura, Masaki; Hongo, Daigo; Nabeshima, Tatsuya
Twofold fused concave hosts containing two phosphorus atoms: modules for the sandwich-type encapsulation of fullerenes in variable cavities
Chem. Sci., 2015, 6, 6373
1529287 CIFC50 H52 Cl12 O6 P2P 1 21/c 112.0579; 17.329; 27.445
90; 91.263; 90
5733.3Yamamura, Masaki; Hongo, Daigo; Nabeshima, Tatsuya
Twofold fused concave hosts containing two phosphorus atoms: modules for the sandwich-type encapsulation of fullerenes in variable cavities
Chem. Sci., 2015, 6, 6373
1529288 CIFC152 H96 O12 P4P 1 21/c 124.148; 23.858; 22.983
90; 117.759; 90
11717Yamamura, Masaki; Hongo, Daigo; Nabeshima, Tatsuya
Twofold fused concave hosts containing two phosphorus atoms: modules for the sandwich-type encapsulation of fullerenes in variable cavities
Chem. Sci., 2015, 6, 6373
1529289 CIFC152 H96 O12 P4C 1 2/m 134.54; 42.038; 17.4446
90; 100.248; 90
24925Yamamura, Masaki; Hongo, Daigo; Nabeshima, Tatsuya
Twofold fused concave hosts containing two phosphorus atoms: modules for the sandwich-type encapsulation of fullerenes in variable cavities
Chem. Sci., 2015, 6, 6373
1529290 CIFC156 H100 Cl12 O12 P4C 1 2/c 125.827; 22.684; 22.259
90; 99.466; 90
12863Yamamura, Masaki; Hongo, Daigo; Nabeshima, Tatsuya
Twofold fused concave hosts containing two phosphorus atoms: modules for the sandwich-type encapsulation of fullerenes in variable cavities
Chem. Sci., 2015, 6, 6373
1529291 CIFC164 H98 Cl6 O12 P4P 21 21 221.98; 17.101; 17.472
90; 90; 90
6567Yamamura, Masaki; Hongo, Daigo; Nabeshima, Tatsuya
Twofold fused concave hosts containing two phosphorus atoms: modules for the sandwich-type encapsulation of fullerenes in variable cavities
Chem. Sci., 2015, 6, 6373
1529292 CIFC166 H100 Cl12 O12 P4C 1 2/c 134.079; 13.764; 27.024
90; 103.463; 90
12328Yamamura, Masaki; Hongo, Daigo; Nabeshima, Tatsuya
Twofold fused concave hosts containing two phosphorus atoms: modules for the sandwich-type encapsulation of fullerenes in variable cavities
Chem. Sci., 2015, 6, 6373
1529293 CIFC21 H22 N2 O2P 21 21 218.8494; 10.974; 17.557
90; 90; 90
1705Komine, Keita; Nomura, Yusuke; Ishihara, Jun; Hatakeyama, Susumi
Total Synthesis of (-)-N-Methylwelwitindolinone C Isothiocyanate Based on a Pd-Catalyzed Tandem Enolate Coupling Strategy.
Organic letters, 2015, 17, 3918-3921
1529294 CIFC22 H20 N2 OP -110.3796; 12.9633; 14.3864
71.474; 71.763; 68.137
1661.2Komine, Keita; Nomura, Yusuke; Ishihara, Jun; Hatakeyama, Susumi
Total Synthesis of (-)-N-Methylwelwitindolinone C Isothiocyanate Based on a Pd-Catalyzed Tandem Enolate Coupling Strategy.
Organic letters, 2015, 17, 3918-3921
1529295 CIFC39 H58 Cl Cr N2 O5P 1 21/c 114.615; 16.834; 16.342
90; 112.456; 90
3716Devaine-Pressing, Katalin; Dawe, Louise N.; Kozak, Christopher M.
Cyclohexene oxide/carbon dioxide copolymerization by chromium(iii) amino-bis(phenolato) complexes and MALDI-TOF MS analysis of the polycarbonates
Polym. Chem., 2015, 6, 6305
1529296 CIFC38.5 H51 Cl4 Cr N4 O4P -18.751; 11.96; 20.098
95.039; 97.965; 92.325
2072.2Devaine-Pressing, Katalin; Dawe, Louise N.; Kozak, Christopher M.
Cyclohexene oxide/carbon dioxide copolymerization by chromium(iii) amino-bis(phenolato) complexes and MALDI-TOF MS analysis of the polycarbonates
Polym. Chem., 2015, 6, 6305
1529297 CIFC38 H54 Cl Cr N2 O6P c a 2117.119; 11.491; 37.818
90; 90; 90
7439Devaine-Pressing, Katalin; Dawe, Louise N.; Kozak, Christopher M.
Cyclohexene oxide/carbon dioxide copolymerization by chromium(iii) amino-bis(phenolato) complexes and MALDI-TOF MS analysis of the polycarbonates
Polym. Chem., 2015, 6, 6305
1529298 CIFC40 H44 N4 O6P 1 21 19.9993; 12.9855; 13.4171
90; 110.184; 90
1635.17Zhang, Wei; Huang, Xiao-Jun; Zhang, Sheng-Yuan; Zhang, Dong-Mei; Jiang, Ren-Wang; Hu, Jian-Yang; Zhang, Xiao-Qi; Wang, Lei; Ye, Wen-Cai
Geleganidines A-C, Unusual Monoterpenoid Indole Alkaloids from Gelsemium elegans.
Journal of natural products, 2015, 78, 2036-2044
1529299 CIFC43 H68 N6 O9P 1 21 18.3147; 19.2037; 14.1567
90; 102.128; 90
2210Cayuela, Angelina; Kennedy, Stuart R.; Soriano, M. Laura; Jones, Christopher D.; Valcárcel, Miguel; Steed, Jonathan W.
Fluorescent carbon dot‒molecular salt hydrogels
Chem. Sci., 2015, 6, 6139
1529300 CIFC13 H14 N3 O2P 1 21/c 18.5132; 21.0477; 7.2003
90; 113.595; 90
1182.31Weiss, Ryan J.; Gordts, Philip L. S. M.; Le, Dzung; Xu, Ding; Esko, Jeffrey D.; Tor, Yitzhak
Small molecule antagonists of cell-surface heparan sulfate and heparin‒protein interactions
Chem. Sci., 2015, 6, 5984
1529301 CIFC13 H18 N3 O3P -16.2877; 8.8655; 12.0399
102.993; 91.548; 92.63
652.79Weiss, Ryan J.; Gordts, Philip L. S. M.; Le, Dzung; Xu, Ding; Esko, Jeffrey D.; Tor, Yitzhak
Small molecule antagonists of cell-surface heparan sulfate and heparin‒protein interactions
Chem. Sci., 2015, 6, 5984
1529302 CIFC24 H29 Cl2 N6 O5P 1 21/m 15.0339; 37.994; 7.136
90; 110.533; 90
1278.1Weiss, Ryan J.; Gordts, Philip L. S. M.; Le, Dzung; Xu, Ding; Esko, Jeffrey D.; Tor, Yitzhak
Small molecule antagonists of cell-surface heparan sulfate and heparin‒protein interactions
Chem. Sci., 2015, 6, 5984
1529303 CIFC26 H26 F7.5 N6 Na0.5 O9C 1 2/m 114.0292; 22.3313; 9.5059
90; 92.95; 90
2974.2Weiss, Ryan J.; Gordts, Philip L. S. M.; Le, Dzung; Xu, Ding; Esko, Jeffrey D.; Tor, Yitzhak
Small molecule antagonists of cell-surface heparan sulfate and heparin‒protein interactions
Chem. Sci., 2015, 6, 5984
1529304 CIFC9 H12 O3P 1 21/c 19.0223; 35.5424; 9.3818
90; 118.65; 90
2640.2Feghali, Elias; Carrot, Géraldine; Thuéry, Pierre; Genre, Caroline; Cantat, Thibault
Convergent reductive depolymerization of wood lignin to isolated phenol derivatives by metal-free catalytic hydrosilylation
Energy Environ. Sci., 2015, 8, 2734
1529305 CIFC9 H12 O2P c a 2118.8855; 7.9784; 11.2136
90; 90; 90
1689.62Feghali, Elias; Carrot, Géraldine; Thuéry, Pierre; Genre, Caroline; Cantat, Thibault
Convergent reductive depolymerization of wood lignin to isolated phenol derivatives by metal-free catalytic hydrosilylation
Energy Environ. Sci., 2015, 8, 2734
1529306 CIFC15 H20 O4P 1 21 17.9409; 6.3235; 13.5701
90; 97.834; 90
675.05Hyldgaard, Mette G.; Purup, Stig; Bond, Andrew D.; Fretté, Xavier C; Qu, Haiyan; Jensen, Katrine T.; Christensen, Lars P.
Guaianolides and a seco-Eudesmane from the Resinous Exudates of Cushion Bush (Leucophyta brownii) and Evaluation of Their Cytostatic and Anti-inflammatory Activity.
Journal of natural products, 2015, 78, 1877-1885
1529307 CIFC29 H36 O7 SiP 1 21/c 114.1631; 11.4869; 16.4977
90; 94.808; 90
2674.57Sakata, Juri; Ando, Yoshio; Ohmori, Ken; Suzuki, Keisuke
Synthetic Study on Naphthospironone A: Construction of Benzobicyclo[3.2.1]octene Skeleton with Oxaspirocycle.
Organic letters, 2015, 17, 3746-3749
1529308 CIFC106 H120 Cl6 N8 PtP 1 21/c 120.8774; 15.8099; 30.488
90; 99.1261; 90
9935.8Jiang, Hua-Wei; Tanaka, Takayuki; Osuka, Atsuhiro
Singly and doubly β-to-β platinum-bridged porphyrin dimers and their reductive eliminations
Chem. Sci., 2015, 6, 6102
1529309 CIFC111 H123 Cl9 N8 O4 Pt Zn2P -114.8426; 20.11; 21.2677
63.3696; 78.2695; 71.6398
5371.33Jiang, Hua-Wei; Tanaka, Takayuki; Osuka, Atsuhiro
Singly and doubly β-to-β platinum-bridged porphyrin dimers and their reductive eliminations
Chem. Sci., 2015, 6, 6102
1529310 CIFC147.31 H169.64 Cl21.9 N8 Ni2 Pt2P -119.4832; 20.2466; 21.267
86.76; 81.4; 67.434
7659.8Jiang, Hua-Wei; Tanaka, Takayuki; Osuka, Atsuhiro
Singly and doubly β-to-β platinum-bridged porphyrin dimers and their reductive eliminations
Chem. Sci., 2015, 6, 6102
1529311 CIFC164.8 H174 Cl12 N8 Ni2 O P2 PtC 1 2/c 164.086; 12.967; 40.547
90; 102.6; 90
32883Jiang, Hua-Wei; Tanaka, Takayuki; Osuka, Atsuhiro
Singly and doubly β-to-β platinum-bridged porphyrin dimers and their reductive eliminations
Chem. Sci., 2015, 6, 6102
1529312 CIFC107 H113 Cl3 N10 Zn2C 1 2/c 131.53; 8.731; 36.552
90; 113.582; 90
9222Jiang, Hua-Wei; Tanaka, Takayuki; Osuka, Atsuhiro
Singly and doubly β-to-β platinum-bridged porphyrin dimers and their reductive eliminations
Chem. Sci., 2015, 6, 6102
1529313 CIFC27 H29 Br N O6 PP 110.2391; 11.4922; 24.9637
91.304; 98.318; 114.935
2624.1Horwitz, Matthew A.; Tanaka, Naoya; Yokosaka, Takuya; Uraguchi, Daisuke; Johnson, Jeffrey S.; Ooi, Takashi
Enantioselective reductive multicomponent coupling reactions between isatins and aldehydes.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 6086-6090
1529314 CIFC52 H66 Co2 F12 N8 O5P 1 21/n 110.072; 38.683; 14.706
90; 98.28; 90
5670Villanueva, Omar; Weldy, Nina Mace; Blakey, Simon B.; MacBeth, Cora E.
Cobalt catalyzed sp3C‒H amination utilizing aryl azides
Chem. Sci., 2015, 6, 6672
1529315 CIFC44 H52 Co2 K2 N6 O4F d d d10.8136; 27.533; 29.5266
90; 90; 90
8791Villanueva, Omar; Weldy, Nina Mace; Blakey, Simon B.; MacBeth, Cora E.
Cobalt catalyzed sp3C‒H amination utilizing aryl azides
Chem. Sci., 2015, 6, 6672
1529316 CIFC70 H79 Co2 N9 O4P 32 2 114.064; 14.064; 27.143
90; 90; 120
4649.5Villanueva, Omar; Weldy, Nina Mace; Blakey, Simon B.; MacBeth, Cora E.
Cobalt catalyzed sp3C‒H amination utilizing aryl azides
Chem. Sci., 2015, 6, 6672
1529317 CIFC16 H14 I N5P 1 21 18.499; 8.394; 11.73
90; 104.19; 90
811.292Scheuermann, Thomas H.; Stroud, Daniel; Sleet, Christopher E.; Bayeh, Liela; Shokri, Cameron; Wang, Hanzhi; Caldwell, Charles G.; Longgood, Jamie; MacMillan, John B.; Bruick, Richard K.; Gardner, Kevin H.; Tambar, Uttam K.
Isoform-Selective and Stereoselective Inhibition of Hypoxia Inducible Factor-2.
Journal of medicinal chemistry, 2015, 58, 5930-5941
1529318 CIFC19 H18 O8P 1 21/c 113.6047; 7.4884; 17.5684
90; 101.622; 90
1753.13Liu, Yayue; Yang, Qin; Xia, Guoping; Huang, Hongbo; Li, Hanxiang; Ma, Lin; Lu, Yongjun; He, Lei; Xia, Xuekui; She, Zhigang
Polyketides with α-Glucosidase Inhibitory Activity from a Mangrove Endophytic Fungus, Penicillium sp. HN29-3B1.
Journal of natural products, 2015, 78, 1816-1822
1529319 CIF
HKL
Fe2 Ge4 Li Na O12C 1 2/c 110.03328; 8.81362; 5.529646
90; 108.921; 90
462.561T.V. Drokina; G.A. Petrakovskii; M.S. Molokeev; S.V. Misyul; V.S. Bondarev; D.A. Velikanov; M. Frontzek; J. Schefer
Crystal and magnetic structures, phase transitions in quasi-one-dimensional pyroxenes Na0.5Li0.5FeGe2O6
Journal of Magnetism and Magnetic Materials, 2015, 385, 243-249
1529320 CIF
HKL
Fe2 Ge4 Li Na O12P 1 21/c 19.9692; 8.85448; 5.47516
90; 108.494; 90
458.34T.V. Drokina; G.A. Petrakovskii; M.S. Molokeev; S.V. Misyul; V.S. Bondarev; D.A. Velikanov; M. Frontzek; J. Schefer
Crystal and magnetic structures, phase transitions in quasi-one-dimensional pyroxenes Na0.5Li0.5FeGe2O6
Journal of Magnetism and Magnetic Materials, 2015, 385, 243-249
1529321 CIFC56 H68 N4 O13F 4 3 236.2659; 36.2659; 36.2659
90; 90; 90
47697.5Barker, Emily C.; Goh, Ching Yong; Jones, Franca; Mocerino, Mauro; Skelton, Brian W.; Becker, Thomas; Ogden, Mark I.
Investigating hydrogel formation using in situ variable-temperature scanning probe microscopy
Chem. Sci., 2015, 6, 6133
1529322 CIFC24 H27 N O3P -111.3191; 11.464; 18.1291
93.847; 101.554; 114.578
2065.9Tan, Wei Wen; Yoshikai, Naohiko
Copper-catalyzed condensation of imines and α-diazo-β-dicarbonyl compounds: modular and regiocontrolled synthesis of multisubstituted pyrroles
Chem. Sci., 2015, 6, 6448
1529323 CIFC27 H23 N O3P 1 21/c 19.9721; 14.3477; 15.3171
90; 106.912; 90
2096.7Tan, Wei Wen; Yoshikai, Naohiko
Copper-catalyzed condensation of imines and α-diazo-β-dicarbonyl compounds: modular and regiocontrolled synthesis of multisubstituted pyrroles
Chem. Sci., 2015, 6, 6448
1529324 CIFC25 H19 Bi F9 N5 O9 S3P -19.3667; 13.6119; 13.6823
77.1774; 87.8299; 79.1523
1670.6Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Patrick, Brian O.; McDonald, Robert; Ferguson, Michael J.
Bipyridine complexes of E3+(E = P, As, Sb, Bi): strong Lewis acids, sources of E(OTf)3and synthons for EIand EVcations
Chem. Sci., 2015, 6, 6545
1529325 CIFC41 H51 F9 N5 O9 P S3P -111.6535; 14.5562; 14.588
88.2712; 80.7875; 88.0482
2440.47Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Patrick, Brian O.; McDonald, Robert; Ferguson, Michael J.
Bipyridine complexes of E3+(E = P, As, Sb, Bi): strong Lewis acids, sources of E(OTf)3and synthons for EIand EVcations
Chem. Sci., 2015, 6, 6545
1529326 CIFC44.67 H56.5 As F9 N6.83 O9 S3P -115.0217; 18.4434; 31.1243
93.909; 101.339; 99.3536
8297.5Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Patrick, Brian O.; McDonald, Robert; Ferguson, Michael J.
Bipyridine complexes of E3+(E = P, As, Sb, Bi): strong Lewis acids, sources of E(OTf)3and synthons for EIand EVcations
Chem. Sci., 2015, 6, 6545
1529327 CIFC41 H51 F9 N5 O9 S3 SbP 1 21/n 114.0078; 17.6534; 22.0396
90; 108.34; 90
5173.3Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Patrick, Brian O.; McDonald, Robert; Ferguson, Michael J.
Bipyridine complexes of E3+(E = P, As, Sb, Bi): strong Lewis acids, sources of E(OTf)3and synthons for EIand EVcations
Chem. Sci., 2015, 6, 6545
1529328 CIFC27 H34.5 F9 N7.5 O9 P S3P -113.2699; 15.788; 20.4958
76.0415; 87.922; 73.566
3994.6Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Patrick, Brian O.; McDonald, Robert; Ferguson, Michael J.
Bipyridine complexes of E3+(E = P, As, Sb, Bi): strong Lewis acids, sources of E(OTf)3and synthons for EIand EVcations
Chem. Sci., 2015, 6, 6545
1529329 CIFC28 H36 As F9 N8 O9 S3P -112.3457; 13.3802; 14.5721
81.4461; 66.6056; 72.0828
2101.1Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Patrick, Brian O.; McDonald, Robert; Ferguson, Michael J.
Bipyridine complexes of E3+(E = P, As, Sb, Bi): strong Lewis acids, sources of E(OTf)3and synthons for EIand EVcations
Chem. Sci., 2015, 6, 6545
1529330 CIFC27 H22 F9 N6 O9 P S3C 1 2/c 128.5371; 13.8414; 21.8775
90; 124.553; 90
7117.1Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Patrick, Brian O.; McDonald, Robert; Ferguson, Michael J.
Bipyridine complexes of E3+(E = P, As, Sb, Bi): strong Lewis acids, sources of E(OTf)3and synthons for EIand EVcations
Chem. Sci., 2015, 6, 6545
1529344 CIFC13 H18 Br O6 P SP 1 21/c 112.3376; 19.514; 7.6624
90; 102.727; 90
1799.4Rodrigues, Alessandro; Olivato, Paulo R.; Zukerman-Schpector, Julio; Maganhi, Stella H.; Reis, Adriana K. C. A.; Tiekink, Edward R. T.
Molecular Structures of Isomeric Ortho, Meta, and Para Bromo-Substituted α-Methylsulfonyl-α-diethoxyphosphoryl Acetophenones by X-ray and DFT Molecular Orbital Calculations.
The journal of physical chemistry. A, 2015, 119, 8714-8723
1529345 CIFC41 H59 B Ir N O2 P2P -114.2754; 16.7152; 18.3801
66.601; 89.641; 87.421
4020.7Lee, Chun-I; DeMott, Jessica C.; Pell, Christopher J.; Christopher, Alyson; Zhou, Jia; Bhuvanesh, Nattamai; Ozerov, Oleg V.
Ligand survey results in identification of PNP pincer complexes of iridium as long-lived and chemoselective catalysts for dehydrogenative borylation of terminal alkynes
Chem. Sci., 2015, 6, 6572
1529346 CIFC38 H64 B2 Ir N O4 P2P 1 21/c 115.139; 11.8769; 23.409
90; 95.654; 90
4188.6Lee, Chun-I; DeMott, Jessica C.; Pell, Christopher J.; Christopher, Alyson; Zhou, Jia; Bhuvanesh, Nattamai; Ozerov, Oleg V.
Ligand survey results in identification of PNP pincer complexes of iridium as long-lived and chemoselective catalysts for dehydrogenative borylation of terminal alkynes
Chem. Sci., 2015, 6, 6572
1529347 CIFC47 H61 B F4 Ir N O2 P2P 1 21/c 114.781; 26.065; 12.544
90; 107.16; 90
4618Lee, Chun-I; DeMott, Jessica C.; Pell, Christopher J.; Christopher, Alyson; Zhou, Jia; Bhuvanesh, Nattamai; Ozerov, Oleg V.
Ligand survey results in identification of PNP pincer complexes of iridium as long-lived and chemoselective catalysts for dehydrogenative borylation of terminal alkynes
Chem. Sci., 2015, 6, 6572
1529348 CIFC32 H53 B Ir N O2 P2P 1 21/c 114.792; 17.546; 14.1242
90; 110.435; 90
3435.1Lee, Chun-I; DeMott, Jessica C.; Pell, Christopher J.; Christopher, Alyson; Zhou, Jia; Bhuvanesh, Nattamai; Ozerov, Oleg V.
Ligand survey results in identification of PNP pincer complexes of iridium as long-lived and chemoselective catalysts for dehydrogenative borylation of terminal alkynes
Chem. Sci., 2015, 6, 6572
1529349 CIFC36 H62 Cl2 Cu2 O6 P2 S2P 1 21 110.6416; 13.3076; 17.3445
90; 92.328; 90
2454.2Wang, Ding; Cao, Peng; Wang, Bing; Jia, Tao; Lou, Yazhou; Wang, Min; Liao, Jian
Copper(I)-Catalyzed Asymmetric Pinacolboryl Addition of N-Boc-imines Using a Chiral Sulfoxide-Phosphine Ligand.
Organic letters, 2015, 17, 2420-2423
1529350 CIFC16 H10 Br F3 N2 O2 SI 1 2/a 111.4371; 13.3473; 22.4306
90; 101.301; 90
3357.74Lee, Eunsook; Ryu, Taekyu; Shin, Eunji; Son, Jeong-Yu; Choi, Wonseok; Lee, Phil Ho
Synthesis of 2-bromoimidazoles from alkynes, N-sulfonylazides, and bromocyanides.
Organic letters, 2015, 17, 2470-2473
1529351 CIFC4 H48 K0.28 N16 Ni2 O4 Rb7.72 Si18C 1 2/c 130.669; 9.919; 19.894
90; 110.18; 90
5680Gärtner, Stefanie; Hamberger, Markus; Korber, Nikolaus
The First Chelate-Free Crystal Structure of a Silicide Transition Metal Complex [K0.28Rb7.72Si9Ni(CO)2]2·16NH3
Crystals, 2015, 5, 275
1529352 CIFC20 H9 N3 O9 S4P 1 21/n 18.0275; 7.8676; 34.961
90; 90.106; 90
2208Salmerón-Valverde, Amparo; Bernès, Sylvain
Two Closely Related Organic Charge-Transfer Complexes Based on Tetrathiafulvalene and 9H-fluorenone Derivatives. Competition between Hydrogen Bonding and Stacking Interactions
Crystals, 2015, 5, 283
1529353 CIFC21 H11 N3 O9 S4P 1 21/n 119.078; 7.2068; 19.443
90; 117.833; 90
2364Salmerón-Valverde, Amparo; Bernès, Sylvain
Two Closely Related Organic Charge-Transfer Complexes Based on Tetrathiafulvalene and 9H-fluorenone Derivatives. Competition between Hydrogen Bonding and Stacking Interactions
Crystals, 2015, 5, 283
1529354 CIFC14 H22 O2 SeP 1 2/c 18.7358; 9.1761; 19.689
90; 116.096; 90
1417.4Prasad, Poonam Rajesh; Singh, Harkesh B.; Butcher, Ray J.
Synthesis, Structure and Antioxidant Activity of Cyclohexene-Fused Selenuranes and Related Derivatives.
Molecules (Basel, Switzerland), 2015, 20, 12670-12685
1529355 CIFC14 H16 O4 TeP b c a15.7046; 8.83038; 19.1603
90; 90; 90
2657.1Prasad, Poonam Rajesh; Singh, Harkesh B.; Butcher, Ray J.
Synthesis, Structure and Antioxidant Activity of Cyclohexene-Fused Selenuranes and Related Derivatives.
Molecules (Basel, Switzerland), 2015, 20, 12670-12685
1529356 CIFC14 H16 O4 SeC 1 2/c 115.034; 8.5925; 10.4102
90; 112.358; 90
1243.69Prasad, Poonam Rajesh; Singh, Harkesh B.; Butcher, Ray J.
Synthesis, Structure and Antioxidant Activity of Cyclohexene-Fused Selenuranes and Related Derivatives.
Molecules (Basel, Switzerland), 2015, 20, 12670-12685
1529357 CIFC6 H14 Mn N8 O8P -15.2482; 6.533; 10.6128
90.532; 102.774; 109.139
333.93Liu, Bing; Fernandes, José A; Tomé, João P C; Paz, Filipe A Almeida; Cunha-Silva, Luís
Multidimensional Transition Metal Complexes Based on 3-Amino-1H-1,2,4-triazole-5-carboxylic Acid: From Discrete Mononuclear Complexes to Layered Materials.
Molecules (Basel, Switzerland), 2015, 20, 12341-12363
1529358 CIFC6 H8 N8 O5 ZnP b c n9.537; 6.865; 17.12
90; 90; 90
1120.9Liu, Bing; Fernandes, José A; Tomé, João P C; Paz, Filipe A Almeida; Cunha-Silva, Luís
Multidimensional Transition Metal Complexes Based on 3-Amino-1H-1,2,4-triazole-5-carboxylic Acid: From Discrete Mononuclear Complexes to Layered Materials.
Molecules (Basel, Switzerland), 2015, 20, 12341-12363
1529359 CIFC3 H6 Mn N4 O4P 1 21/c 18.1472; 9.9846; 9.3679
90; 113.994; 90
696.2Liu, Bing; Fernandes, José A; Tomé, João P C; Paz, Filipe A Almeida; Cunha-Silva, Luís
Multidimensional Transition Metal Complexes Based on 3-Amino-1H-1,2,4-triazole-5-carboxylic Acid: From Discrete Mononuclear Complexes to Layered Materials.
Molecules (Basel, Switzerland), 2015, 20, 12341-12363
1529360 CIFC6 H8 Cd N8 O5P 1 21/n 18.9893; 8.9785; 13.9642
90; 108.117; 90
1071.2Liu, Bing; Fernandes, José A; Tomé, João P C; Paz, Filipe A Almeida; Cunha-Silva, Luís
Multidimensional Transition Metal Complexes Based on 3-Amino-1H-1,2,4-triazole-5-carboxylic Acid: From Discrete Mononuclear Complexes to Layered Materials.
Molecules (Basel, Switzerland), 2015, 20, 12341-12363
1529361 CIFC12 H26 Fe2 N16 O16P n n a27.111; 12.697; 7.7352
90; 90; 90
2662.7Liu, Bing; Fernandes, José A; Tomé, João P C; Paz, Filipe A Almeida; Cunha-Silva, Luís
Multidimensional Transition Metal Complexes Based on 3-Amino-1H-1,2,4-triazole-5-carboxylic Acid: From Discrete Mononuclear Complexes to Layered Materials.
Molecules (Basel, Switzerland), 2015, 20, 12341-12363
1529362 CIFC32 H22 N6P 1 21/c 115.6612; 9.6881; 16.3377
90; 96.112; 90
2464.8Constantinides, Christos P.; Zissimou, Georgia A.; Berezin, Andrey A.; Ioannou, Theodosia A.; Manoli, Maria; Tsokkou, Demetra; Theodorou, Eleni; Hayes, Sophia C.; Koutentis, Panayiotis A.
Tetraphenylhexaazaanthracenes: 16π Weakly Antiaromatic Species with Singlet Ground States.
Organic letters, 2015, 17, 4026-4029
1529363 CIFC34 H26 Cl2 N6P -18.8511; 9.8863; 16.5742
107.267; 92.876; 90.368
1382.87Constantinides, Christos P.; Zissimou, Georgia A.; Berezin, Andrey A.; Ioannou, Theodosia A.; Manoli, Maria; Tsokkou, Demetra; Theodorou, Eleni; Hayes, Sophia C.; Koutentis, Panayiotis A.
Tetraphenylhexaazaanthracenes: 16π Weakly Antiaromatic Species with Singlet Ground States.
Organic letters, 2015, 17, 4026-4029
1529364 CIFC24 H41 F8 N2 Ni O3 PP 1 21/c 115.5474; 9.9548; 19.6379
90; 92.862; 90
3035.6Andrella, Nicholas O.; Sicard, Alexandre J.; Gorelsky, Serge I.; Korobkov, Ilia; Baker, R. Tom
A T-shaped Ni[κ2-(CF2)4‒] NHC complex: unusual Csp3‒F and M‒CFbond functionalization reactions
Chem. Sci., 2015, 6, 6392
1529365 CIFC31 H38 F8 N2 NiP 21 21 2110.8851; 15.544; 18.9208
90; 90; 90
3201.4Andrella, Nicholas O.; Sicard, Alexandre J.; Gorelsky, Serge I.; Korobkov, Ilia; Baker, R. Tom
A T-shaped Ni[κ2-(CF2)4‒] NHC complex: unusual Csp3‒F and M‒CFbond functionalization reactions
Chem. Sci., 2015, 6, 6392
1529366 CIFC35 H45 F10 N2 Ni O3 SP 1 21/c 110.2361; 16.5042; 22.6115
90; 90.96; 90
3819.4Andrella, Nicholas O.; Sicard, Alexandre J.; Gorelsky, Serge I.; Korobkov, Ilia; Baker, R. Tom
A T-shaped Ni[κ2-(CF2)4‒] NHC complex: unusual Csp3‒F and M‒CFbond functionalization reactions
Chem. Sci., 2015, 6, 6392
1529367 CIFC33 H41 F7 N2 Ni O2P 1 21/c 19.7181; 18.216; 19.2228
90; 92.18; 90
3400.5Andrella, Nicholas O.; Sicard, Alexandre J.; Gorelsky, Serge I.; Korobkov, Ilia; Baker, R. Tom
A T-shaped Ni[κ2-(CF2)4‒] NHC complex: unusual Csp3‒F and M‒CFbond functionalization reactions
Chem. Sci., 2015, 6, 6392
1529368 CIFC37 H46 F8 N2 Ni OP 1 21/c 116.5255; 10.6186; 20.8839
90; 101.931; 90
3585.5Andrella, Nicholas O.; Sicard, Alexandre J.; Gorelsky, Serge I.; Korobkov, Ilia; Baker, R. Tom
A T-shaped Ni[κ2-(CF2)4‒] NHC complex: unusual Csp3‒F and M‒CFbond functionalization reactions
Chem. Sci., 2015, 6, 6392
1529370 CIFC22 H18 F3 N O4 SP 1 21/c 115.9; 21.601; 19.802
90; 110.332; 90
6377.4Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun
Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes.
Organic letters, 2015, 17, 3944-3947
1529371 CIFC28 H24 F3 N O5 SP -112.978; 13.576; 16.636
84.126; 79.909; 65.828
2631.2Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun
Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes.
Organic letters, 2015, 17, 3944-3947
1529372 CIFC28 H24 F3 N O4 SP 1 21/n 115.6589; 9.9834; 16.2519
90; 92.274; 90
2538.6Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun
Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes.
Organic letters, 2015, 17, 3944-3947
1529373 CIFC24 H24 F3 N O4 SP -110.562; 11.1083; 11.2554
85.47; 66.868; 84.789
1208Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun
Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes.
Organic letters, 2015, 17, 3944-3947
1529374 CIFC22 H20 N2 O2 SP 1 21/c 111.5958; 12.0999; 14.031
90; 97.891; 90
1950Zeng, Ting-Ting; Xuan, Jun; Ding, Wei; Wang, Kuan; Lu, Liang-Qiu; Xiao, Wen-Jing
[3 + 2] Cycloaddition/Oxidative Aromatization Sequence via Photoredox Catalysis: One-Pot Synthesis of Oxazoles from 2H-Azirines and Aldehydes.
Organic letters, 2015, 17, 4070-4073
1529375 CIFC104 N6 O82 P2 Ti4 W20P 1 21/n 123.1112; 15.2701; 27.7104
90; 108.738; 90
9260.94Takahashi, Eri; Kamata, Keigo; Kikukawa, Yuji; Sato, Sota; Suzuki, Kosuke; Yamaguchi, Kazuya; Mizuno, Noritaka
Synthesis and oxidation catalysis of a Ti-substituted phosphotungstate, and identification of the active oxygen species
Catal. Sci. Technol., 2015, 5, 4778
1529376 CIFO80 P2 Ti4 W20P -120.57; 34.716; 54.711
88.88; 85.12; 79.8
38312Takahashi, Eri; Kamata, Keigo; Kikukawa, Yuji; Sato, Sota; Suzuki, Kosuke; Yamaguchi, Kazuya; Mizuno, Noritaka
Synthesis and oxidation catalysis of a Ti-substituted phosphotungstate, and identification of the active oxygen species
Catal. Sci. Technol., 2015, 5, 4778
1529377 CIFC23 H19 N OP -19.4895; 9.9809; 18.7212
88.615; 83.84; 89.586
1762.4Zhang, Chunyan; Liu, Jianhua; Xia, Chungu
Palladium‒N-heterocyclic carbene (NHC)-catalyzed synthesis of 2-ynamides via oxidative aminocarbonylation of alkynes with amines
Catal. Sci. Technol., 2015, 5, 4750
1529378 CIFC87 H75 N4 O4P -111.962; 15.81; 19.746
97.277; 99.848; 100.275
3572Katoono, Ryo; Kawai, Shunsuke; Fujiwara, Kenshu; Suzuki, Takanori
Controllability of dynamic double helices: quantitative analysis of the inversion of a screw-sense preference upon complexation
Chem. Sci., 2015, 6, 6592
1529381 CIFC114 H172 Cl K Li0 N47 O38C 1 2/c 129.3719; 14.1615; 33.703
90; 101.172; 90
13753.1Lu, Xiaoyong; Isaacs, Lyle
Synthesis and Recognition Properties of Enantiomerically Pure Acyclic Cucurbit[n]uril-Type Molecular Containers.
Organic letters, 2015, 17, 4038-4041
1529389 CIFC68 H60 Ce Li4 N12F d d d :211.4483; 43.06; 24.522
90; 90; 90
12088.5Levin, Jessica R.; Dorfner, Walter L.; Carroll, Patrick J.; Schelter, Eric J.
Control of cerium oxidation state through metal complex secondary structures
Chem. Sci., 2015, 6, 6925
1529390 CIFC88 H80 Ce N16 Na4P -113.9504; 16.2467; 19.0053
83.136; 83.696; 84.993
4238.8Levin, Jessica R.; Dorfner, Walter L.; Carroll, Patrick J.; Schelter, Eric J.
Control of cerium oxidation state through metal complex secondary structures
Chem. Sci., 2015, 6, 6925
1529391 CIFC83 H75 Ce K5 N15P -115.2003; 15.4668; 18.0353
93.849; 101.333; 107.292
3933.7Levin, Jessica R.; Dorfner, Walter L.; Carroll, Patrick J.; Schelter, Eric J.
Control of cerium oxidation state through metal complex secondary structures
Chem. Sci., 2015, 6, 6925
1529392 CIFC32 H36 N2 O2P n a 2130.3531; 5.0918; 16.0639
90; 90; 90
2482.71Takagi, K.; Kato, R.; Yamamoto, S.; Masu, H.
Amide-bridged ladder poly(p-phenylene): synthesis by direct arylation and π-stacked assembly
Polym. Chem., 2015, 6, 6792
1529393 CIFC25 H24 Cl N O5P 21 21 216.9051; 18.0332; 18.2794
90; 90; 90
2276.2Liu, Qiong-Jie; Yan, Wen-Guang; Wang, Lijia; Zhang, X. Peter; Tang, Yong
One-Pot Catalytic Asymmetric Synthesis of Tetrahydrocarbazoles.
Organic letters, 2015, 17, 4014-4017
1529394 CIFC96 H130 N4 O6 Si4 Y2P -110.7741; 13.3826; 16.275
82.3193; 83.5313; 77.923
2265.39Altenbuchner, P. T.; Adams, F.; Kronast, A.; Herdtweck, E.; Pöthig, A.; Rieger, B.
Stereospecific catalytic precision polymerization of 2-vinylpyridine via rare earth metal-mediated group transfer polymerization with 2-methoxyethylamino-bis(phenolate)-yttrium complexes
Polym. Chem., 2015, 6, 6796
1529395 CIFC9 H13 I O4C 1 2 117.7416; 5.1188; 12.1148
90; 92.9213; 90
1098.78Lan, Ping; White, Lauren E.; Taher, Ehab S.; Guest, Prudence E.; Banwell, Martin G.; Willis, Anthony C.
Chemoenzymatic Synthesis of (+)-Asperpentyn and the Enantiomer of the Structure Assigned to Aspergillusol A.
Journal of natural products, 2015, 78, 1963-1968
1529396 CIFC26 H18 N2 O11P 1 21 121.6418; 6.1229; 21.6668
90; 116.016; 90
2580.2Lan, Ping; White, Lauren E.; Taher, Ehab S.; Guest, Prudence E.; Banwell, Martin G.; Willis, Anthony C.
Chemoenzymatic Synthesis of (+)-Asperpentyn and the Enantiomer of the Structure Assigned to Aspergillusol A.
Journal of natural products, 2015, 78, 1963-1968
1529397 CIFC11 H14 Cl I O4P 21 21 215.5023; 8.005; 31.0282
90; 90; 90
1366.67Lan, Ping; White, Lauren E.; Taher, Ehab S.; Guest, Prudence E.; Banwell, Martin G.; Willis, Anthony C.
Chemoenzymatic Synthesis of (+)-Asperpentyn and the Enantiomer of the Structure Assigned to Aspergillusol A.
Journal of natural products, 2015, 78, 1963-1968
1529398 CIFC25 H23 N O6C 1 2/c 131.5153; 8.7548; 18.0436
90; 123.435; 90
4154.5Huang, Jing-Kai; Yang Lauderdale, Tsai-Ling; Shia, Kak-Shan
Studies on Antibiotics Active against Resistant Bacteria. Total Synthesis of MRSA-Active Tetarimycin A and Its Analogues.
Organic letters, 2015, 17, 4248-4251
1529399 CIFC55 H35 B F2 N2P 1 21/c 116.4511; 17.491; 13.5624
90; 98.856; 90
3856Chua, Ming Hui; Huang, Kuo-Wei; Xu, Jianwei; Wu, Jishan
Unusual Intramolecular Hydrogen Transfer in 3,5-Di(triphenylethylenyl) BODIPY Synthesis and 1,2-Migratory Shift in Subsequent Scholl Type Reaction.
Organic letters, 2015, 17, 4168-4171
1529400 CIFC55 H36 B F7 N2P 1 21/c 113.1321; 10.7218; 30.2961
90; 96.85; 90
4235.23Chua, Ming Hui; Huang, Kuo-Wei; Xu, Jianwei; Wu, Jishan
Unusual Intramolecular Hydrogen Transfer in 3,5-Di(triphenylethylenyl) BODIPY Synthesis and 1,2-Migratory Shift in Subsequent Scholl Type Reaction.
Organic letters, 2015, 17, 4168-4171
1529401 CIFC55 H41 B F2 N2C 1 2/c 121.491; 13.7296; 29.3488
90; 106.144; 90
8318.3Chua, Ming Hui; Huang, Kuo-Wei; Xu, Jianwei; Wu, Jishan
Unusual Intramolecular Hydrogen Transfer in 3,5-Di(triphenylethylenyl) BODIPY Synthesis and 1,2-Migratory Shift in Subsequent Scholl Type Reaction.
Organic letters, 2015, 17, 4168-4171
1529402 CIFC19 H20 Br N OP 1 21 15.225; 13.44; 11.8487
90; 90.133; 90
832.06Dziechciejewski, Wojciech J.; Weber, Regina; Sowada, Oliver; Boysen, Mike M. K.
Cycloalkene Carbonitriles in Rhodium-Catalyzed 1,4-Addition and Formal Synthesis of Vabicaserin.
Organic letters, 2015, 17, 4132-4135
1529403 CIFC57 H79 Br2 N4 Si2C 1 2/c 138.86; 15.6626; 22.7308
90; 125.774; 90
11224.8Arz, Marius I.; Geiß, Daniel; Straßmann, Martin; Schnakenburg, Gregor; Filippou, Alexander C.
Silicon(i) chemistry: the NHC-stabilised silicon(i) halides Si2X2(Idipp)2(X = Br, I) and the disilicon(i)-iodido cation [Si2(I)(Idipp)2]+
Chem. Sci., 2015, 6, 6515
1529404 CIFC57 H79 I2 N4 Si2C 1 2/c 138.872; 15.6801; 22.7851
90; 125.507; 90
11305.4Arz, Marius I.; Geiß, Daniel; Straßmann, Martin; Schnakenburg, Gregor; Filippou, Alexander C.
Silicon(i) chemistry: the NHC-stabilised silicon(i) halides Si2X2(Idipp)2(X = Br, I) and the disilicon(i)-iodido cation [Si2(I)(Idipp)2]+
Chem. Sci., 2015, 6, 6515
1529405 CIFC84 H77 B F21 I N4 Si2P 1 21/n 119.9019; 20.2022; 20.2072
90; 99.189; 90
8020.3Arz, Marius I.; Geiß, Daniel; Straßmann, Martin; Schnakenburg, Gregor; Filippou, Alexander C.
Silicon(i) chemistry: the NHC-stabilised silicon(i) halides Si2X2(Idipp)2(X = Br, I) and the disilicon(i)-iodido cation [Si2(I)(Idipp)2]+
Chem. Sci., 2015, 6, 6515
1529406 CIFC21 H46 Br N O2P 1 21/c 122.8075; 7.3222; 14.4685
90; 94.765; 90
2407.9Dai, Caili; Wu, Xuepeng; Li, Weitao; You, Qin; Zhao, Mingwei; Du, Mingyong; Liu, Yifei; Li, Yuyang
The role of hydroxyethyl groups in the construction of wormlike micelles in the system of quaternary ammonium surfactant and sodium salicylate.
Soft matter, 2015, 11, 7817-7826
1529407 CIFC166 H146 B4 Cr2 N12P -115.3682; 15.9908; 17.5923
72.813; 69.832; 68.859
3712.1DeGayner, Jordan A.; Jeon, Ie-Rang; Harris, T. David
A series of tetraazalene radical-bridged M2(M = CrIII, MnII, FeII, CoII) complexes with strong magnetic exchange coupling
Chem. Sci., 2015, 6, 6639
1529408 CIFC134 H90 B2 F48 Mn2 N12P -115.0589; 15.8311; 18.4096
75.382; 67.031; 68.819
3736DeGayner, Jordan A.; Jeon, Ie-Rang; Harris, T. David
A series of tetraazalene radical-bridged M2(M = CrIII, MnII, FeII, CoII) complexes with strong magnetic exchange coupling
Chem. Sci., 2015, 6, 6639
1529409 CIFC140 H102 B2 F48 Fe2 N12 O1.5P -115.1719; 15.9218; 18.3985
75.334; 66.781; 68.243
3763.5DeGayner, Jordan A.; Jeon, Ie-Rang; Harris, T. David
A series of tetraazalene radical-bridged M2(M = CrIII, MnII, FeII, CoII) complexes with strong magnetic exchange coupling
Chem. Sci., 2015, 6, 6639
1529410 CIFC134 H76 B2 Co2 F48 N12P -114.8476; 15.9017; 18.21
75.56; 67.648; 68.82
3676.39DeGayner, Jordan A.; Jeon, Ie-Rang; Harris, T. David
A series of tetraazalene radical-bridged M2(M = CrIII, MnII, FeII, CoII) complexes with strong magnetic exchange coupling
Chem. Sci., 2015, 6, 6639
1529411 CIFC292 H264 B6 Cr4 N28P -115.17; 15.9112; 30.3415
90.924; 97.35; 115.288
6546.9DeGayner, Jordan A.; Jeon, Ie-Rang; Harris, T. David
A series of tetraazalene radical-bridged M2(M = CrIII, MnII, FeII, CoII) complexes with strong magnetic exchange coupling
Chem. Sci., 2015, 6, 6639
1529415 CIFC21 H23 Cl O3 SP -19.0302; 10.7298; 13.2534
93.47; 92.319; 93.973
1277.4Chen, Zhen-Zhen; Liu, Shuai; Hao, Wen-Juan; Xu, Ge; Wu, Shuo; Miao, Jiao-Na; Jiang, Bo; Wang, Shu-Liang; Tu, Shu-Jiang; Li, Guigen
Catalytic arylsulfonyl radical-triggered 1,5-enyne-bicyclizations and hydrosulfonylation of α,β-conjugates.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 6654-6658
1529420 CIFC21 H23 Cl F2 N2 OC 1 c 113.1195; 25.1207; 6.0786
90; 103.299; 90
1949.6Chen, Qiao; Zhou, Jiawei; Wang, Yanan; Wang, Chao; Liu, Xihong; Xu, Zhaoqing; Lin, Li; Wang, Rui
Transition-Metal-Free Dehydrosilylative Difluoroamidation of Tetrahydroisoquinolines under Mild Conditions.
Organic letters, 2015, 17, 4212-4215
1529421 CIFC13 H18 O4P 1 21 15.917; 7.864; 13.651
90; 101.24; 90
623Rybak, Taras; Hall, Dennis G.
Stereoselective and Regiodivergent Allylic Suzuki-Miyaura Cross-Coupling of 2-Ethoxydihydropyranyl Boronates: Synthesis and Confirmation of Absolute Stereochemistry of Diospongin B.
Organic letters, 2015, 17, 4156-4159
1529422 CIFC13 H18 O3P 1 21/n 19.7101; 10.6909; 23.0359
90; 92.6548; 90
2388.78Rybak, Taras; Hall, Dennis G.
Stereoselective and Regiodivergent Allylic Suzuki-Miyaura Cross-Coupling of 2-Ethoxydihydropyranyl Boronates: Synthesis and Confirmation of Absolute Stereochemistry of Diospongin B.
Organic letters, 2015, 17, 4156-4159
1529423 CIFC42 H33 Cl2 Ir N2 O5P 1 21/n 118.021; 10.891; 18.559
90; 103.69; 90
3539Zhou, Tao; Li, Liubo; Li, Bin; Song, Haibin; Wang, Baiquan
Ir(III)-Catalyzed Oxidative Coupling of NH Isoquinolones with Benzoquinone.
Organic letters, 2015, 17, 4204-4207
1529424 CIFC28 H18 Cl2 N2 O5P -110.069; 10.87; 12.021
71.67; 82.11; 82.87
1232.5Zhou, Tao; Li, Liubo; Li, Bin; Song, Haibin; Wang, Baiquan
Ir(III)-Catalyzed Oxidative Coupling of NH Isoquinolones with Benzoquinone.
Organic letters, 2015, 17, 4204-4207
1529425 CIFC131 H158 N8 O15 P6 Pt3P 63/m23.8013; 23.8013; 13.6022
90; 90; 120
6673.3Loughrey, Jonathan J.; Patmore, Nathan J.; Baldansuren, Amgalanbaatar; Fielding, Alistair J.; McInnes, Eric J. L.; Hardie, Michaele J.; Sproules, Stephen; Halcrow, Malcolm A.
Platinum(ii) complexes of mixed-valent radicals derived from cyclotricatechylene, a macrocyclic tris-dioxolene
Chem. Sci., 2015, 6, 6935
1529426 CIFC104.7 H101.78 N1.3 O9.84 P6 Pt3P 1 21 114.86; 23.898; 15.103
90; 98.87; 90
5299.3Loughrey, Jonathan J.; Patmore, Nathan J.; Baldansuren, Amgalanbaatar; Fielding, Alistair J.; McInnes, Eric J. L.; Hardie, Michaele J.; Sproules, Stephen; Halcrow, Malcolm A.
Platinum(ii) complexes of mixed-valent radicals derived from cyclotricatechylene, a macrocyclic tris-dioxolene
Chem. Sci., 2015, 6, 6935
1529427 CIFC52.59 H37.19 Cl1.19 N6 O4F d d d23.5964; 37.347; 40.0789
90; 90; 90
35319.7Windle, Christopher D.; George, Michael W.; Perutz, Robin N.; Summers, Peter A.; Sun, Xue Zhong; Whitwood, Adrian C.
Comparison of rhenium‒porphyrin dyads for CO2photoreduction: photocatalytic studies and charge separation dynamics studied by time-resolved IR spectroscopy
Chem. Sci., 2015, 6, 6847
1529428 CIFC67.5 H49 Cl5 F6 N8 O4 P Re ZnP -112.9474; 15.8804; 17.3277
98.752; 92.264; 106.821
3357.4Windle, Christopher D.; George, Michael W.; Perutz, Robin N.; Summers, Peter A.; Sun, Xue Zhong; Whitwood, Adrian C.
Comparison of rhenium‒porphyrin dyads for CO2photoreduction: photocatalytic studies and charge separation dynamics studied by time-resolved IR spectroscopy
Chem. Sci., 2015, 6, 6847
1529429 CIFC15 H17 F3 O3P 21 21 218.511; 11.945; 14.173
90; 90; 90
1440.9Yang, Zhong-Jin; Ge, Wei-Zhi; Li, Qiu-Ying; Lu, Yaxin; Gong, Jian-Miao; Kuang, Bei-Jia; Xi, Xiaonan; Wu, Haiting; Zhang, Quan; Chen, Yue
Syntheses and Biological Evaluation of Costunolide, Parthenolide, and Their Fluorinated Analogues.
Journal of medicinal chemistry, 2015, 58, 7007-7020
1529442 CIFC305 Al334 N38 Na296 O3692 Si1106I m -3 m45.0711; 45.0711; 45.0711
90; 90; 90
91557.6Guo, Peng; Shin, Jiho; Greenaway, Alex G.; Min, Jung Gi; Su, Jie; Choi, Hyun June; Liu, Leifeng; Cox, Paul A.; Hong, Suk Bong; Wright, Paul A.; Zou, Xiaodong
A zeolite family with expanding structural complexity and embedded isoreticular structures
Nature, 2015, 524, 74-78
1529443 CIFAl325 Na285 O3726 Si1115I m -3 m44.9242; 44.9242; 44.9242
90; 90; 90
90665Guo, Peng; Shin, Jiho; Greenaway, Alex G.; Min, Jung Gi; Su, Jie; Choi, Hyun June; Liu, Leifeng; Cox, Paul A.; Hong, Suk Bong; Wright, Paul A.; Zou, Xiaodong
A zeolite family with expanding structural complexity and embedded isoreticular structures
Nature, 2015, 524, 74-78
1529444 CIFC448 Al638 N56 Na162 O5843 Si2002 Sr210I m -3 m55.0437; 55.0437; 55.0437
90; 90; 90
166772Guo, Peng; Shin, Jiho; Greenaway, Alex G.; Min, Jung Gi; Su, Jie; Choi, Hyun June; Liu, Leifeng; Cox, Paul A.; Hong, Suk Bong; Wright, Paul A.; Zou, Xiaodong
A zeolite family with expanding structural complexity and embedded isoreticular structures
Nature, 2015, 524, 74-78
1529445 CIFC448 Al638 N56 Na560 O5866 Si2002 Sr11I m -3 m55.0664; 55.0664; 55.0664
90; 90; 90
166978Guo, Peng; Shin, Jiho; Greenaway, Alex G.; Min, Jung Gi; Su, Jie; Choi, Hyun June; Liu, Leifeng; Cox, Paul A.; Hong, Suk Bong; Wright, Paul A.; Zou, Xiaodong
A zeolite family with expanding structural complexity and embedded isoreticular structures
Nature, 2015, 524, 74-78
1529446 CIFC24 H32 O4P 1 21 17.04536; 13.74167; 11.14078
90; 93.7268; 90
1076.31Wu, Ping; Yao, Lei; Xu, Liangxiong; Xue, Jinghua; Wei, Xiaoyi
Bisacremines A-D, Dimeric Acremines Produced by a Soil-Derived Acremonium persicinum Strain.
Journal of natural products, 2015, 78, 2161-2166
1529447 CIFC35 H40 O9P 21 21 219.1983; 18.6272; 18.7098
90; 90; 90
3205.71Ning, Ruonan; Lei, Yun; Liu, Shuangzhu; Wang, Huan; Zhang, Rujun; Wang, Wei; Zhu, Yingdong; Zhang, Haiyan; Zhao, Weimin
Natural β-Dihydroagarofuran-Type Sesquiterpenoids as Cognition-Enhancing and Neuroprotective Agents from Medicinal Plants of the Genus Celastrus.
Journal of natural products, 2015, 78, 2175-2186
1529448 CIFC15 H18 Cl N O2P -111.1941; 11.9877; 12.3151
117.921; 101.02; 90.422
1424.3Deng, Yongming; Jing, Changcheng; Zavalij, Peter Y.; Doyle, Michael P.
Hg(OTf)2 Catalyzed Intramolecular 1,4-Addition of Donor-Acceptor Cyclopropenes to Arenes.
Organic letters, 2015, 17, 4312-4315
1529449 CIFC14 H10 Br NP 1 21/n 19.7442; 13.1654; 17.8252
90; 93.934; 90
2281.3Messaoud, Mohamed Yacine Ameur; Bentabed-Ababsa, Ghenia; Hedidi, Madani; Derdour, Aïcha; Chevallier, Floris; Halauko, Yury S.; Ivashkevich, Oleg A.; Matulis, Vadim E.; Picot, Laurent; Thiéry, Valérie; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence
Deproto-metallation of N-arylated pyrroles and indoles using a mixed lithium-zinc base and regioselectivity-computed CH acidity relationship.
Beilstein journal of organic chemistry, 2015, 11, 1475-1485
1529450 CIFC14 H10 I NC 1 c 17.08; 20.666; 8.2442
90; 100.632; 90
1185.54Messaoud, Mohamed Yacine Ameur; Bentabed-Ababsa, Ghenia; Hedidi, Madani; Derdour, Aïcha; Chevallier, Floris; Halauko, Yury S.; Ivashkevich, Oleg A.; Matulis, Vadim E.; Picot, Laurent; Thiéry, Valérie; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence
Deproto-metallation of N-arylated pyrroles and indoles using a mixed lithium-zinc base and regioselectivity-computed CH acidity relationship.
Beilstein journal of organic chemistry, 2015, 11, 1475-1485
1529451 CIFC11 H10 I N OP 1 21/n 19.9461; 6.9825; 15.2049
90; 92.314; 90
1055.1Messaoud, Mohamed Yacine Ameur; Bentabed-Ababsa, Ghenia; Hedidi, Madani; Derdour, Aïcha; Chevallier, Floris; Halauko, Yury S.; Ivashkevich, Oleg A.; Matulis, Vadim E.; Picot, Laurent; Thiéry, Valérie; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence
Deproto-metallation of N-arylated pyrroles and indoles using a mixed lithium-zinc base and regioselectivity-computed CH acidity relationship.
Beilstein journal of organic chemistry, 2015, 11, 1475-1485
1529452 CIFC10 H7 Br I NP 1 21/n 110.0665; 5.9895; 17.5155
90; 103.942; 90
1024.96Messaoud, Mohamed Yacine Ameur; Bentabed-Ababsa, Ghenia; Hedidi, Madani; Derdour, Aïcha; Chevallier, Floris; Halauko, Yury S.; Ivashkevich, Oleg A.; Matulis, Vadim E.; Picot, Laurent; Thiéry, Valérie; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence
Deproto-metallation of N-arylated pyrroles and indoles using a mixed lithium-zinc base and regioselectivity-computed CH acidity relationship.
Beilstein journal of organic chemistry, 2015, 11, 1475-1485
1529453 CIFC14 H13 N3 OP 1 21/n 111.4222; 5.4888; 19.7338
90; 100.562; 90
1216.23Messaoud, Mohamed Yacine Ameur; Bentabed-Ababsa, Ghenia; Hedidi, Madani; Derdour, Aïcha; Chevallier, Floris; Halauko, Yury S.; Ivashkevich, Oleg A.; Matulis, Vadim E.; Picot, Laurent; Thiéry, Valérie; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence
Deproto-metallation of N-arylated pyrroles and indoles using a mixed lithium-zinc base and regioselectivity-computed CH acidity relationship.
Beilstein journal of organic chemistry, 2015, 11, 1475-1485
1529454 CIFC34 H38 N3 O7 PP 21 21 219.9296; 13.1794; 24.2673
90; 90; 90
3175.8Otsuka, M.; Maeno, Y.; Fukami, T.; Inoue, M.; Tagami, T.; Ozeki, T.
Developmental considerations for ethanolates with regard to stability and physicochemical characterization of efonidipine hydrochloride ethanolate
CrystEngComm, 2015, 17, 7430
1529455 CIFC36 H45 Cl N3 O8 PP -111.4763; 11.9281; 15.1054
87.156; 78.155; 64.918
1831.3Otsuka, M.; Maeno, Y.; Fukami, T.; Inoue, M.; Tagami, T.; Ozeki, T.
Developmental considerations for ethanolates with regard to stability and physicochemical characterization of efonidipine hydrochloride ethanolate
CrystEngComm, 2015, 17, 7430
1529456 CIFC14 H13 N O5 PbP -4 21 c19.0391; 19.0391; 8.0073
90; 90; 90
2902.54Knichal, Jane V.; Gee, William J.; Burrows, Andrew D.; Raithby, Paul R.; Wilson, Chick C.
A new small molecule gelator and 3D framework ligator of lead(ii)
CrystEngComm, 2015, 17, 8139
1529457 CIFC22 H26 O6P 1 21 111.4215; 32.7681; 11.5118
90; 116.753; 90
3847.22Lu, Yuanyuan; Xue, Yongbo; Liu, Junjun; Yao, Guangmin; Li, Dongyan; Sun, Bin; Zhang, Jinwen; Liu, Yanfei; Qi, Changxing; Xiang, Ming; Luo, Zengwei; Du, Guang; Zhang, Yonghui
(±)-Acortatarinowins A-F, Norlignan, Neolignan, and Lignan Enantiomers from Acorus tatarinowii.
Journal of natural products, 2015, 78, 2205-2214
1529458 CIFC29 H32 O5P b c a24.274; 16.262; 12.626
90; 90; 90
4984Rouger, Caroline; Derbré, Séverine; Charreau, Béatrice; Pabois, Angélique; Cauchy, Thomas; Litaudon, Marc; Awang, Khalijah; Richomme, Pascal
Lepidotol A from Mesua lepidota Inhibits Inflammatory and Immune Mediators in Human Endothelial Cells.
Journal of natural products, 2015, 78, 2187-2197
1529460 CIFBa3 O8 P2R -3 m :H5.6019; 5.6019; 20.9878
90; 90; 120
570.39Haipeng Ji; Zhaohui Huang; Zhiguo Xia; Maxim S. Molokeev; Victor V. Atuchin; Minghao Fang; Yangai Liu
Discovery of New Solid Solution Phosphors via Cation Substitution-Dependent Phase Transition in M3(PO4)2:Eu2+ (M = Ca/Sr/Ba) Quasi-Binary Sets
The Journal of Physical Chemistry C, 2015, 119, 2038-2045
1529461 CIFBa0.81 O4 P Sr0.69R -3 m :H5.54011; 5.54011; 20.6573
90; 90; 120
549.09Haipeng Ji; Zhaohui Huang; Zhiguo Xia; Maxim S. Molokeev; Victor V. Atuchin; Minghao Fang; Yangai Liu
Discovery of New Solid Solution Phosphors via Cation Substitution-Dependent Phase Transition in M3(PO4)2:Eu2+ (M = Ca/Sr/Ba) Quasi-Binary Sets
The Journal of Physical Chemistry C, 2015, 119, 2038-2045
1529462 CIFBa1.16 O12 P3 Sr3.34R -3 m :H5.46471; 5.46471; 20.22347
90; 90; 120
523.023Haipeng Ji; Zhaohui Huang; Zhiguo Xia; Maxim S. Molokeev; Victor V. Atuchin; Minghao Fang; Yangai Liu
Discovery of New Solid Solution Phosphors via Cation Substitution-Dependent Phase Transition in M3(PO4)2:Eu2+ (M = Ca/Sr/Ba) Quasi-Binary Sets
The Journal of Physical Chemistry C, 2015, 119, 2038-2045
1529463 CIF
HKL
O8 P2 Sr3R -3 m :H5.387993; 5.387993; 19.78604
90; 90; 120
497.443Haipeng Ji; Zhaohui Huang; Zhiguo Xia; Maxim S. Molokeev; Victor V. Atuchin; Minghao Fang; Yangai Liu
Discovery of New Solid Solution Phosphors via Cation Substitution-Dependent Phase Transition in M3(PO4)2:Eu2+ (M = Ca/Sr/Ba) Quasi-Binary Sets
The Journal of Physical Chemistry C, 2015, 119, 2038-2045
1529464 CIF
HKL
Ca0.5 O4 P Sr1.05R 3 c :H10.66855; 10.66855; 38.9832
90; 90; 120
3842.54Haipeng Ji; Zhaohui Huang; Zhiguo Xia; Maxim S. Molokeev; Victor V. Atuchin; Minghao Fang; Yangai Liu
Discovery of New Solid Solution Phosphors via Cation Substitution-Dependent Phase Transition in M3(PO4)2:Eu2+ (M = Ca/Sr/Ba) Quasi-Binary Sets
The Journal of Physical Chemistry C, 2015, 119, 2038-2045
1529465 CIF
HKL
Ca O4 P Sr0.43R 3 c :H10.56198; 10.56198; 38.0712
90; 90; 120
3678.1Haipeng Ji; Zhaohui Huang; Zhiguo Xia; Maxim S. Molokeev; Victor V. Atuchin; Minghao Fang; Yangai Liu
Discovery of New Solid Solution Phosphors via Cation Substitution-Dependent Phase Transition in M3(PO4)2:Eu2+ (M = Ca/Sr/Ba) Quasi-Binary Sets
The Journal of Physical Chemistry C, 2015, 119, 2038-2045
1529466 CIF
HKL
Ca11 O28 P7R 3 c :H10.4414; 10.4414; 37.4208
90; 90; 120
3533.14Haipeng Ji; Zhaohui Huang; Zhiguo Xia; Maxim S. Molokeev; Victor V. Atuchin; Minghao Fang; Yangai Liu
Discovery of New Solid Solution Phosphors via Cation Substitution-Dependent Phase Transition in M3(PO4)2:Eu2+ (M = Ca/Sr/Ba) Quasi-Binary Sets
The Journal of Physical Chemistry C, 2015, 119, 2038-2045
1529467 CIFC18 H15 N3P 1 21/c 115.885; 7.4464; 25.627
90; 104.762; 90
2931.3Fu, Hualong; Cui, Mengchao; Zhao, Liu; Tu, Peiyu; Zhou, Kaixiang; Dai, Jiapei; Liu, Boli
Highly Sensitive Near-Infrared Fluorophores for in Vivo Detection of Amyloid-β Plaques in Alzheimer's Disease.
Journal of medicinal chemistry, 2015, 58, 6972-6983
1529468 CIFC20 H17 N3P 1 21/c 117.171; 7.611; 25.394
90; 95.737; 90
3302.1Fu, Hualong; Cui, Mengchao; Zhao, Liu; Tu, Peiyu; Zhou, Kaixiang; Dai, Jiapei; Liu, Boli
Highly Sensitive Near-Infrared Fluorophores for in Vivo Detection of Amyloid-β Plaques in Alzheimer's Disease.
Journal of medicinal chemistry, 2015, 58, 6972-6983
1529469 CIFC22 H35 N O3P 21 21 216.212; 12.231; 28.133
90; 90; 90
2137.5Zhang, Dewu; Tao, Xiaoyu; Chen, Ridao; Liu, Jimei; Li, Li; Fang, Xiaomei; Yu, Liyan; Dai, Jungui
Pericoannosin A, a Polyketide Synthase-Nonribosomal Peptide Synthetase Hybrid Metabolite with New Carbon Skeleton from the Endophytic Fungus Periconia sp.
Organic letters, 2015, 17, 4304-4307
1529470 CIFC22 H33 N O3.5P 21 21 2112.515; 14.907; 45.898
90; 90; 90
8563Zhang, Dewu; Tao, Xiaoyu; Chen, Ridao; Liu, Jimei; Li, Li; Fang, Xiaomei; Yu, Liyan; Dai, Jungui
Pericoannosin A, a Polyketide Synthase-Nonribosomal Peptide Synthetase Hybrid Metabolite with New Carbon Skeleton from the Endophytic Fungus Periconia sp.
Organic letters, 2015, 17, 4304-4307
1529471 CIFC56.5 H50 B2 F15 Mg N3 O3P -111.7916; 13.46; 18.239
86.434; 88.133; 69.802
2711.3Lampland, Nicole L.; Pindwal, Aradhana; Neal, Steven R.; Schlauderaff, Shealyn; Ellern, Arkady; Sadow, Aaron D.
Magnesium-catalyzed hydrosilylation of α,β-unsaturated esters
Chem. Sci., 2015, 6, 6901
1529472 CIFC6 H6 Cd3 N8 O6F d d 212.808; 24.306; 7.7275
90; 90; 90
2406Wu, Mei-Feng; Shen, Ting-Ting; He, Shuai; Wu, Ke-Qin; Wang, Shuai-Hua; Liu, Zhi-Fa; Zheng, Fa-Kun; Guo, Guo-Cong
An unprecedented organic‒inorganic hybrid material with an I3O3framework based on cadmium hydroxide and in situ generated 1H-tetrazolate-5-acetic acid
CrystEngComm, 2015, 17, 7473
1529473 CIFC28 H29 N5 O4P -17.7823; 10.8987; 15.2414
72.781; 83.016; 85.094
1224Samanta, Ritwik; Kumar, B. Sathish; Panda, Pradeepta K.
Calix[4]pyrroles with Shortest Possible Strap: Exclusively Selective toward Fluoride Ion.
Organic letters, 2015, 17, 4140-4143
1529474 CIFC15 H21 I OC 1 2 122.448; 6.0248; 11.443
90; 97.517; 90
1534.3Shen, Zhigao; Pan, Xixian; Lai, Yisheng; Hu, Jiadong; Wan, Xiaolong; Li, Xiaoge; Zhang, Hui; Xie, Weiqing
Chiral ion-pair organocatalyst promotes highly enantioselective 3-exo iodo-cycloetherification of allyl alcohols
Chem. Sci., 2015, 6, 6986
1529475 CIFC19 H19 I N4 O4P 1 21 110.31; 7.955; 11.875
90; 90.15; 90
973.9Shen, Zhigao; Pan, Xixian; Lai, Yisheng; Hu, Jiadong; Wan, Xiaolong; Li, Xiaoge; Zhang, Hui; Xie, Weiqing
Chiral ion-pair organocatalyst promotes highly enantioselective 3-exo iodo-cycloetherification of allyl alcohols
Chem. Sci., 2015, 6, 6986
1529476 CIFC22 H18 Br2 O4P 3 c 140.346; 40.346; 17.984
90; 90; 120
25352White, Nicholas G.; MacLachlan, Mark J.
Anion-templated hexagonal nanotubes
Chem. Sci., 2015, 6, 6245
1529477 CIFC54 H90 Br2 N2 O4P 3 c 140.346; 40.346; 17.984
90; 90; 120
25352White, Nicholas G.; MacLachlan, Mark J.
Anion-templated hexagonal nanotubes
Chem. Sci., 2015, 6, 6245
1529478 CIFC54 H88 Br2 N2 O6R 3 c :H39.973; 39.973; 18.0631
90; 90; 120
24995White, Nicholas G.; MacLachlan, Mark J.
Anion-templated hexagonal nanotubes
Chem. Sci., 2015, 6, 6245
1529479 CIFC54 H88 Br2 N2 O6R 3 c :H39.896; 39.896; 18.0796
90; 90; 120
24922White, Nicholas G.; MacLachlan, Mark J.
Anion-templated hexagonal nanotubes
Chem. Sci., 2015, 6, 6245
1529480 CIF
HKL
Ca12 Ga8 Ge12 O48I a -3 d12.25619; 12.25619; 12.25619
90; 90; 90
1841.05Chengyin Liu; Zhiguo Xia; Maxim S. Molokeev; Quanlin Liu
Synthesis, Crystal Structure, and Enhanced Luminescence of Garnet-Type Ca3Ga2Ge3O12:Cr3+ by Codoping Bi3+
Journal of the American Ceramic Society, 2015, 98, 1870-1876
1529481 CIF
HKL
Er0.24 Gd6.96 O48 W12 Yb0.8C 1 2/c 17.65407; 11.41403; 11.39088
90; 109.744; 90
936.65Mengyan Yin; Yangai Liu; Lefu Mei; Maxim S. Molokeev; Zhaohui Huang; Minghao Fang
Preparation, crystal structure and up-conversion luminescence of Er3+, Yb3+ co-doped Gd2(WO4)3
RSC Advances, 2015, 5, 73077-73082
1529487 CIF
HKL
Bi2 Cs4 Mo6 Na2 O24R 3 c :H10.652543; 10.652543; 40.96937
90; 90; 120
4026.21A.A. Savina; V.V. Atuchin; S.F. Solodovnikov; Z.A. Solodovnikova; A.S. Krylov; E.A. Maximovskiy; M.S. Molokeev; A.S. Oreshonkov; A.M. Pugachev; E.G. Khaikina
Synthesis, structural and spectroscopic properties of acentric triple molybdate Cs2NaBi(MoO4)3
Journal of Solid State Chemistry, 2015, 225, 53-58
1529489 CIF
HKL
B La5 O13 Si2P 63/m9.55299; 9.55299; 7.21426
90; 90; 120
570.17Zhiguo Xia; Maxim S. Molokeev; Won Bin Im; Sanjith Unithrattil; Quanlin Liu
Crystal Structure and Photoluminescence Evolution of La5(Si2+xB1-x)(O13-xNx):Ce3+ Solid Solution Phosphors
The Journal of Physical Chemistry C, 2015, 119, 9488-9495
1529490 CIF
HKL
La5 N O12 Si3P 63/m9.71207; 9.71207; 7.18946
90; 90; 120
587.29Zhiguo Xia; Maxim S. Molokeev; Won Bin Im; Sanjith Unithrattil; Quanlin Liu
Crystal Structure and Photoluminescence Evolution of La5(Si2+xB1-x)(O13-xNx):Ce3+ Solid Solution Phosphors
The Journal of Physical Chemistry C, 2015, 119, 9488-9495
1529491 CIF
HKL
F2 La7.22 O24 Si6 Sr2.78P 63/m9.85486; 9.85486; 7.30224
90; 90; 120
614.17Qingfeng Guo; Libing Liao; Maxim S. Molokeev; Lefu Mei; Haikun Liu
Color Tunable Emission and Energy Transfer of Ce3+ and Tb3+ co-doped Novel La6Sr4(SiO4)6F2 Phosphors with apatite structure
Materials Research Bulletin, 2015, 72, 245-251
1529492 CIF
HKL
Al4 Mg2 O18 Si5P 6/m c c9.78698; 9.78698; 9.33739
90; 90; 120
774.56Jun Zhou; Zhiguo Xia; Mingyue Chen; Maxim S. Molokeev; Quanlin Liu
New Insight into Phase Formation of MxMg2Al4+xSi5-xO18:Eu2+ Solid Solution Phosphors and Its Luminescence Properties
Scientific Reports, 2015, 5, 12149-12153
1529493 CIF
HKL
Al8.33 K0.34 Mg4 O36 Si9.67P 6/m c c9.79306; 9.79306; 9.33885
90; 90; 120
775.64Jun Zhou; Zhiguo Xia; Mingyue Chen; Maxim S. Molokeev; Quanlin Liu
New Insight into Phase Formation of MxMg2Al4+xSi5-xO18:Eu2+ Solid Solution Phosphors and Its Luminescence Properties
Scientific Reports, 2015, 5, 12149-12153
1529494 CIF
HKL
Al8.51 K0.52 Mg4 O36 Si9.49P 6/m c c9.79423; 9.79423; 9.34129
90; 90; 120
776.03Jun Zhou; Zhiguo Xia; Mingyue Chen; Maxim S. Molokeev; Quanlin Liu
New Insight into Phase Formation of MxMg2Al4+xSi5-xO18:Eu2+ Solid Solution Phosphors and Its Luminescence Properties
Scientific Reports, 2015, 5, 12149-12153
1529495 CIF
HKL
Al9 K Mg4 O36 Si9P 6/m c c9.79964; 9.79964; 9.36376
90; 90; 120
778.76Jun Zhou; Zhiguo Xia; Mingyue Chen; Maxim S. Molokeev; Quanlin Liu
New Insight into Phase Formation of MxMg2Al4+xSi5-xO18:Eu2+ Solid Solution Phosphors and Its Luminescence Properties
Scientific Reports, 2015, 5, 12149-12153
1529496 CIF
HKL
Al9.02 Mg4 O36 Rb0.99 Si8.98P 6/m c c9.79552; 9.79552; 9.37418
90; 90; 120
778.97Jun Zhou; Zhiguo Xia; Mingyue Chen; Maxim S. Molokeev; Quanlin Liu
New Insight into Phase Formation of MxMg2Al4+xSi5-xO18:Eu2+ Solid Solution Phosphors and Its Luminescence Properties
Scientific Reports, 2015, 5, 12149-12153
1529497 CIF
HKL
Al8.51 Mg4 O36 Rb0.52 Si9.49P 6/m c c9.79723; 9.79723; 9.34351
90; 90; 120
776.69Jun Zhou; Zhiguo Xia; Mingyue Chen; Maxim S. Molokeev; Quanlin Liu
New Insight into Phase Formation of MxMg2Al4+xSi5-xO18:Eu2+ Solid Solution Phosphors and Its Luminescence Properties
Scientific Reports, 2015, 5, 12149-12153
1529498 CIF
HKL
Al9 Mg4 O36 Rb Si9P 6/m c c9.79795; 9.79795; 9.3637
90; 90; 120
778.48Jun Zhou; Zhiguo Xia; Mingyue Chen; Maxim S. Molokeev; Quanlin Liu
New Insight into Phase Formation of MxMg2Al4+xSi5-xO18:Eu2+ Solid Solution Phosphors and Its Luminescence Properties
Scientific Reports, 2015, 5, 12149-12153
1529499 CIF
HKL
Er0.04 In7.96 O16 Sr4P n m a9.83173; 3.266226; 11.49502
90; 90; 90
369.136Ming Guan; Hong Zheng; Lefu Mei; Maxim S. Molokeev; Jing Xie; Tao Yang; Xiaowen Wu; Saifang Huang; Zhaohui Huang
Preparation, Structure and Up-conversion Luminescence of Yb3+/Er3+ co-doped SrIn2O4 Phosphors
Journal of the American Ceramic Society, 2015, 98, 1182-1187
1529500 CIF
HKL
Er0.04 In7.56 O16 Sr4 Yb0.4P n m a9.85272; 3.274175; 11.52212
90; 90; 90
371.698Ming Guan; Hong Zheng; Lefu Mei; Maxim S. Molokeev; Jing Xie; Tao Yang; Xiaowen Wu; Saifang Huang; Zhaohui Huang
Preparation, Structure and Up-conversion Luminescence of Yb3+/Er3+ co-doped SrIn2O4 Phosphors
Journal of the American Ceramic Society, 2015, 98, 1182-1187
1529502 CIF
HKL
C14 H22 N2 O3 SP 21 21 219.7454; 11.2225; 13.9171
90; 90; 90
1522.08N.N. Golovnev; M.S. Molokeev; I.V. Sterkhova; Yu.V. Goryunov; V.V. Atuchin
New class of bicyclic compounds derived from thiobarbituric acid with representative compound 1,3-diethyl-7-hydroxy-5,5,7-trimethyl- 2-thioxo-1,2,3,5,6,7-hexahydro-4H-pyrano[2,3-d]pyrimidin-4-one. Preparation, crystal structure, mass spectrometry and IR spectroscopy.
Journal of Molecular Structure, 2015, 1102, 101-107
1529503 CIFC25 H22 Cl3 F3 N2 O2 SP -18.374; 10.228; 16.064
99.954; 98.372; 101.416
1305.1Wei, Qiang; Chen, Jia-Rong; Hu, Xiao-Qiang; Yang, Xiao-Chen; Lu, Bin; Xiao, Wen-Jing
Photocatalytic Radical Trifluoromethylation/Cyclization Cascade: Synthesis of CF3-Containing Pyrazolines and Isoxazolines.
Organic letters, 2015, 17, 4464-4467
1529504 CIFC30 H21 Br2 N3 O2 S2P 1 21/n 18.2952; 20.7323; 22.0577
90; 100.587; 90
3728.9Cho, Ching Mui; Ye, Qun; Neo, Wei Teng; Lin, Tingting; Lu, Xuehong; Xu, Jianwei
Ultrahigh electron-deficient pyrrolo-acenaphtho-pyridazine-dione based donor‒acceptor conjugated polymers for electrochromic applications
Polym. Chem., 2015, 6, 7570
1529505 CIFC30 H21 Br2 N3 O4P -113.4552; 13.6974; 14.8065
78.712; 73.88; 76.746
2526.1Cho, Ching Mui; Ye, Qun; Neo, Wei Teng; Lin, Tingting; Lu, Xuehong; Xu, Jianwei
Ultrahigh electron-deficient pyrrolo-acenaphtho-pyridazine-dione based donor‒acceptor conjugated polymers for electrochromic applications
Polym. Chem., 2015, 6, 7570
1529506 CIFC19 H16 O2C 1 2 114.321; 8.9769; 11.71
90; 91.66; 90
1504.78Lin, Che-Hung; Pursley, Dominik; Klein, Johannes E. M. N.; Teske, Johannes; Allen, Jennifer A.; Rami, Fabian; Köhn, Andreas; Plietker, Bernd
Non-decarbonylative photochemical versus thermal activation of Bu4N[Fe(CO)3(NO)] ‒ the Fe-catalyzed Cloke‒Wilson rearrangement of vinyl and arylcyclopropanes
Chem. Sci., 2015, 6, 7034
1529507 CIFC19 H16 O2P 1 21 16.3155; 7.7433; 15.0935
90; 100.579; 90
725.57Lin, Che-Hung; Pursley, Dominik; Klein, Johannes E. M. N.; Teske, Johannes; Allen, Jennifer A.; Rami, Fabian; Köhn, Andreas; Plietker, Bernd
Non-decarbonylative photochemical versus thermal activation of Bu4N[Fe(CO)3(NO)] ‒ the Fe-catalyzed Cloke‒Wilson rearrangement of vinyl and arylcyclopropanes
Chem. Sci., 2015, 6, 7034
1529508 CIFC19 H16 O2C 1 2 114.3185; 8.9738; 11.7148
90; 91.675; 90
1504.61Lin, Che-Hung; Pursley, Dominik; Klein, Johannes E. M. N.; Teske, Johannes; Allen, Jennifer A.; Rami, Fabian; Köhn, Andreas; Plietker, Bernd
Non-decarbonylative photochemical versus thermal activation of Bu4N[Fe(CO)3(NO)] ‒ the Fe-catalyzed Cloke‒Wilson rearrangement of vinyl and arylcyclopropanes
Chem. Sci., 2015, 6, 7034
1529509 CIFC19 H16 O2P 1 21 16.309; 7.753; 15.117
90; 100.736; 90
726.5Lin, Che-Hung; Pursley, Dominik; Klein, Johannes E. M. N.; Teske, Johannes; Allen, Jennifer A.; Rami, Fabian; Köhn, Andreas; Plietker, Bernd
Non-decarbonylative photochemical versus thermal activation of Bu4N[Fe(CO)3(NO)] ‒ the Fe-catalyzed Cloke‒Wilson rearrangement of vinyl and arylcyclopropanes
Chem. Sci., 2015, 6, 7034
1529510 CIFC35.33 H22.66 F34 N4 O2.33P -113.287; 14.229; 18.87
70.476; 72.879; 85.688
3212.4Kumari, Harshita; Armitage, Sarah E.; Kline, Steven R.; Damodaran, Krishna K.; Kennedy, Stuart R.; Atwood, Jerry L.; Steed, Jonathan W.
Fluorous 'ponytails' lead to strong gelators showing thermally induced structure evolution.
Soft matter, 2015, 11, 8471-8478
1529712 CIFC12 H14 O5P 21 21 217.8143; 7.9133; 18.3147
90; 90; 90
1132.52Liu, Yayue; Yang, Qin; Xia, Guoping; Huang, Hongbo; Li, Hanxiang; Ma, Lin; Lu, Yongjun; He, Lei; Xia, Xuekui; She, Zhigang
Polyketides with α-Glucosidase Inhibitory Activity from a Mangrove Endophytic Fungus, Penicillium sp. HN29-3B1.
Journal of natural products, 2015, 78, 1816-1822
1529713 CIFC45 H35 B2 F4 N5P 1 21/n 116.679; 11.552; 19.833
90; 101.57; 90
3744Kumar, Sunit; Gobeze, Habtom B.; Chatterjee, Tamal; D'Souza, Francis; Ravikanth, Mangalampalli
Directly Connected AzaBODIPY-BODIPY Dyad: Synthesis, Crystal Structure, and Ground- and Excited-State Interactions.
The journal of physical chemistry. A, 2015, 119, 8338-8348
1529846 CIFC4 H6 S3P 1 21/n 15.965; 10.206; 10.513
90; 90.678; 90
640Luo, Ming; Zhang, Xing-Hong; Darensbourg, Donald J.
An Investigation of the Pathways for Oxygen/Sulfur Scramblings during the Copolymerization of Carbon Disulfide and Oxetane
Macromolecules, 2015, 48, 5526
1529847 CIFC21 H22 N2 O2P 1 21 19.702; 7.4213; 12.862
90; 103.265; 90
901.4Komine, Keita; Nomura, Yusuke; Ishihara, Jun; Hatakeyama, Susumi
Total Synthesis of (-)-N-Methylwelwitindolinone C Isothiocyanate Based on a Pd-Catalyzed Tandem Enolate Coupling Strategy.
Organic letters, 2015, 17, 3918-3921
1529848 CIFC17 H20 O6P 1 21/c 113.5566; 9.9192; 12.1878
90; 114.983; 90
1485.55Sakata, Juri; Ando, Yoshio; Ohmori, Ken; Suzuki, Keisuke
Synthetic Study on Naphthospironone A: Construction of Benzobicyclo[3.2.1]octene Skeleton with Oxaspirocycle.
Organic letters, 2015, 17, 3746-3749
1529849 CIFC37 H54 O6 SiP 1 21/c 19.8958; 32.0974; 20.6189
90; 92.873; 90
6540.9Sakata, Juri; Ando, Yoshio; Ohmori, Ken; Suzuki, Keisuke
Synthetic Study on Naphthospironone A: Construction of Benzobicyclo[3.2.1]octene Skeleton with Oxaspirocycle.
Organic letters, 2015, 17, 3746-3749
1529850 CIFC16 H12 Br F2 N3P 1 21/c 115.027; 8.8571; 11.123
90; 96.542; 90
1470.8Okusu, Satoshi; Tokunaga, Etsuko; Shibata, Norio
Difluoromethylation of Terminal Alkynes by Fluoroform.
Organic letters, 2015, 17, 3802-3805
1529851 CIFC16 H10 Br F2 N OP 1 21/n 117.957; 6.8848; 22.81
90; 99.781; 90
2779Okusu, Satoshi; Tokunaga, Etsuko; Shibata, Norio
Difluoromethylation of Terminal Alkynes by Fluoroform.
Organic letters, 2015, 17, 3802-3805
1529852 CIFC43 H37 Br2 Cl Cu N3 O4 P2P n a 2119.3661; 14.8237; 28.5913
90; 90; 90
8207.9Ramakrishna, Kankanala; Murali, Mani; Sivasankar, Chinnappan
Chemoselective Carbene insertion into the N-H Bond over O-H Bond Using a Well-Defined Single Site (P-P)Cu(I) Catalyst.
Organic letters, 2015, 17, 3814-3817
1529853 CIFC17 H19 N O3P -15.7487; 9.5873; 13.7161
85.932; 86.522; 90.042
752.65Ramakrishna, Kankanala; Murali, Mani; Sivasankar, Chinnappan
Chemoselective Carbene insertion into the N-H Bond over O-H Bond Using a Well-Defined Single Site (P-P)Cu(I) Catalyst.
Organic letters, 2015, 17, 3814-3817
1529854 CIFC18 H16 Br N O3 SP 21 21 217.9153; 11.4655; 18.152
90; 90; 90
1647.3Xiao, Yonglong; Wang, Jinxin; Xia, Wenjing; Shu, Shuangjie; Jiao, Shenchao; Zhou, Yu; Liu, Hong
γ-Carbon Activation through N-Heterocyclic Carbene/Brønsted Acids Cooperative Catalysis: A Highly Enantioselective Route to δ-Lactams.
Organic letters, 2015, 17, 3850-3853
1529855 CIFC26 H18 N2 O SP 1 21/n 19.919; 19.032; 11.221
90; 102.942; 90
2064.5Zhu, Yuelu; Li, Cheng; Zhang, Jidong; She, Mengyao; Sun, Wei; Wan, Kerou; Wang, Yaqi; Yin, Bin; Liu, Ping; Li, Jianli
A Facile FeCl3/I2-Catalyzed Aerobic Oxidative Coupling Reaction: Synthesis of Tetrasubstituted Imidazoles from Amidines and Chalcones.
Organic letters, 2015, 17, 3872-3875
1529856 CIFC29 H21 Br N2 OP -19.724; 11.142; 12.91
98.826; 103.604; 112.844
1205.2Zhu, Yuelu; Li, Cheng; Zhang, Jidong; She, Mengyao; Sun, Wei; Wan, Kerou; Wang, Yaqi; Yin, Bin; Liu, Ping; Li, Jianli
A Facile FeCl3/I2-Catalyzed Aerobic Oxidative Coupling Reaction: Synthesis of Tetrasubstituted Imidazoles from Amidines and Chalcones.
Organic letters, 2015, 17, 3872-3875
1529857 CIFC20 H22 N2 O5 SP 21 21 216.8305; 13.7709; 21.5589
90; 90; 90
2027.88Rao, Wei-Hao; Yin, Xue-Song; Shi, Bing-Feng
Catalyst-Controlled Amino- versus Oxy-Acetoxylation of Urea-Tethered Alkenes: Efficient Synthesis of Cyclic Ureas and Isoureas.
Organic letters, 2015, 17, 3758-3761
1529858 CIFC20 H22 N2 O5 SP -15.9849; 8.35; 21.2894
90.789; 92.849; 107.436
1013.32Rao, Wei-Hao; Yin, Xue-Song; Shi, Bing-Feng
Catalyst-Controlled Amino- versus Oxy-Acetoxylation of Urea-Tethered Alkenes: Efficient Synthesis of Cyclic Ureas and Isoureas.
Organic letters, 2015, 17, 3758-3761
1529859 CIFC24 H17 Br F3 N O4P 32 2 112.075; 12.075; 26.601
90; 90; 120
3358.9Zhu, Yuanyuan; Li, Xiaoyuan; Chen, Qiao; Su, Jinhuan; Jia, Fengjing; Qiu, Shuai; Ma, Mingxia; Sun, Quantao; Yan, Wenjin; Wang, Kairong; Wang, Rui
Highly Enantioselective Cascade Reaction Catalyzed by Squaramides: the Synthesis of CF3-Containing Chromanes.
Organic letters, 2015, 17, 3826-3829
1529860 CIFC18 H13 Cl F3 N O4P 21 21 2110.916; 12.171; 27.176
90; 90; 90
3610.6Zhu, Yuanyuan; Li, Xiaoyuan; Chen, Qiao; Su, Jinhuan; Jia, Fengjing; Qiu, Shuai; Ma, Mingxia; Sun, Quantao; Yan, Wenjin; Wang, Kairong; Wang, Rui
Highly Enantioselective Cascade Reaction Catalyzed by Squaramides: the Synthesis of CF3-Containing Chromanes.
Organic letters, 2015, 17, 3826-3829
1529861 CIFC19 H15 Br F3 N O4P 21 21 218.3159; 9.4678; 23.6499
90; 90; 90
1862Zhu, Yuanyuan; Li, Xiaoyuan; Chen, Qiao; Su, Jinhuan; Jia, Fengjing; Qiu, Shuai; Ma, Mingxia; Sun, Quantao; Yan, Wenjin; Wang, Kairong; Wang, Rui
Highly Enantioselective Cascade Reaction Catalyzed by Squaramides: the Synthesis of CF3-Containing Chromanes.
Organic letters, 2015, 17, 3826-3829
1529862 CIFC25 H22 F N3 O3P 1 21/n 111.943; 12.618; 14.512
90; 90.2; 90
2186.9Miao, Jinmin; Yang, Ke; Kurek, Martin; Ge, Haibo
Palladium-Catalyzed Site-Selective Fluorination of Unactivated C(sp(3))-H Bonds.
Organic letters, 2015, 17, 3738-3741
1529863 CIFC25 H26 O2P b c a12.3364; 8.7782; 36.9717
90; 90; 90
4003.7Ackrill, Thomas D.; Sparkes, Hazel A.; Willis, Christine L.
Synthesis of Diarylheptanoid Scaffolds Inspired by Calyxins I and J.
Organic letters, 2015, 17, 3884-3887
1529864 CIFC32 H30 O2P -17.0588; 11.869; 15.6316
105.145; 101.933; 100.657
1196.58Ackrill, Thomas D.; Sparkes, Hazel A.; Willis, Christine L.
Synthesis of Diarylheptanoid Scaffolds Inspired by Calyxins I and J.
Organic letters, 2015, 17, 3884-3887
1529865 CIFC35 H36 O5P 1 21/c 114.7165; 5.7937; 33.4045
90; 101.755; 90
2788.43Ackrill, Thomas D.; Sparkes, Hazel A.; Willis, Christine L.
Synthesis of Diarylheptanoid Scaffolds Inspired by Calyxins I and J.
Organic letters, 2015, 17, 3884-3887
1529866 CIFC24 H23 N O3 SP -19.2832; 10.302; 12.39
76.387; 83.994; 64.267
1037.4Zhang, Xiaojuan; Han, Xiuling; Lu, Xiyan
Cationic Pd(II)-Catalyzed Cyclization of N-Tosyl-aniline Tethered Allenyl Aldehydes with Arylboronic Acids: Diastereo- and Enantioselective Synthesis of Tetrahydroquinoline Derivatives.
Organic letters, 2015, 17, 3910-3913
1529867 CIFC66 H60 Cl9 N6 O6 P3R -3 :H17.622; 17.622; 37.634
90; 90; 120
10121Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao
Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution.
Organic letters, 2015, 17, 3650-3653
1529868 CIFC67 H65 N6 O8 P3P -113.721; 14.84; 15.073
94.518; 91.104; 100.582
3006Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao
Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution.
Organic letters, 2015, 17, 3650-3653
1529869 CIFC67 H63 N8 O6 P3P -113.731; 14.962; 15.117
94.572; 91.24; 101.538
3031Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao
Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution.
Organic letters, 2015, 17, 3650-3653
1529870 CIFC66 H65 N6 O7 P3P -112.58; 13.197; 19.419
80.816; 80.935; 69.837
2969.2Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao
Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution.
Organic letters, 2015, 17, 3650-3653
1529871 CIFC63 H57 N6 O9 P3P 3113.914; 13.914; 28.339
90; 90; 120
4751.4Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao
Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution.
Organic letters, 2015, 17, 3650-3653
1529872 CIFC65 H63 N6 O7 P3 SP -113.123; 13.188; 19.257
73.751; 79.26; 66.588
2925.5Katagiri, Kosuke; Komagawa, Shinsuke; Uchiyama, Masanobu; Yamaguchi, Kentaro; Azumaya, Isao
Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution.
Organic letters, 2015, 17, 3650-3653
1529873 CIFC20 H24 N2 O4P 1 21 111.5233; 7.6374; 11.6452
90; 110.244; 90
961.56Reddy, B. V. Subba; Reddy, C. Ravikumar; Reddy, M. Rajashekhar; Yarlagadda, Suresh; Sridhar, B.
Substrate Directed C-H Activation for the Synthesis of Benzo[c]cinnolines through a Sequential C-C and C-N Bond Formation.
Organic letters, 2015, 17, 3730-3733
1529874 CIFC20 H18 O7P 21 21 215.968; 10.51; 25.663
90; 90; 90
1609.7Zhao, Ming; Onakpa, Monday M.; Santarsiero, Bernard D.; Huang, Xiao-Jun; Zhang, Xiao-Qi; Chen, Jia; Cheng, Jian-Jun; Longnecker, Richard; Che, Chun-Tao
Icacinlactone H and Icacintrichantholide from the Tuber of Icacina trichantha.
Organic letters, 2015, 17, 3834-3837
1529875 CIFC20 H20 O7P 21 21 26.8018; 20.5957; 12.4023
90; 90; 90
1737.41Zhao, Ming; Onakpa, Monday M.; Santarsiero, Bernard D.; Huang, Xiao-Jun; Zhang, Xiao-Qi; Chen, Jia; Cheng, Jian-Jun; Longnecker, Richard; Che, Chun-Tao
Icacinlactone H and Icacintrichantholide from the Tuber of Icacina trichantha.
Organic letters, 2015, 17, 3834-3837
1529876 CIFC23 H27 F3 O7 SP -19.578; 10.805; 12.575
102.754; 97.366; 93.699
1253Qiu, Yi-Feng; Zhu, Xin-Yu; Li, Ying-Xiu; He, Yu-Tao; Yang, Fang; Wang, Jia; Hua, Hui-Liang; Zheng, Lan; Wang, Li-Chen; Liu, Xue-Yuan; Liang, Yong-Min
AgSCF3-Mediated Trifluoromethylthiolation/Radical Cascade Cyclization of 1,6-Enynes.
Organic letters, 2015, 17, 3694-3697
1529877 CIFC22 H21 Cl F3 N O2 S2P 1 21/c 15.4961; 23.714; 17.6522
90; 96.871; 90
2284.2Qiu, Yi-Feng; Zhu, Xin-Yu; Li, Ying-Xiu; He, Yu-Tao; Yang, Fang; Wang, Jia; Hua, Hui-Liang; Zheng, Lan; Wang, Li-Chen; Liu, Xue-Yuan; Liang, Yong-Min
AgSCF3-Mediated Trifluoromethylthiolation/Radical Cascade Cyclization of 1,6-Enynes.
Organic letters, 2015, 17, 3694-3697
1529878 CIFC16 H15 F3 O3 SP 1 21/c 19.9242; 15.9342; 10.0614
90; 106.109; 90
1528.58Qiu, Yi-Feng; Zhu, Xin-Yu; Li, Ying-Xiu; He, Yu-Tao; Yang, Fang; Wang, Jia; Hua, Hui-Liang; Zheng, Lan; Wang, Li-Chen; Liu, Xue-Yuan; Liang, Yong-Min
AgSCF3-Mediated Trifluoromethylthiolation/Radical Cascade Cyclization of 1,6-Enynes.
Organic letters, 2015, 17, 3694-3697
1529879 CIFC14 H12 Br N OP 1 21/c 16.1858; 17.934; 11.7423
90; 101.212; 90
1277.8Haidzinskaya, Tatsiana; Kerchner, Hilary A.; Liu, Jixin; Watson, Mary P.
Diastereoselective, Zinc-Catalyzed Alkynylation of α-Bromo Oxocarbenium Ions.
Organic letters, 2015, 17, 3857-3859
1529880 CIFC12 H13 Br O3P 1 21/c 15.7983; 8.1321; 24.8527
90; 90.153; 90
1171.86Haidzinskaya, Tatsiana; Kerchner, Hilary A.; Liu, Jixin; Watson, Mary P.
Diastereoselective, Zinc-Catalyzed Alkynylation of α-Bromo Oxocarbenium Ions.
Organic letters, 2015, 17, 3857-3859
1529881 CIFC14 H15 N3 O2P 1 21/n 16.6041; 7.3454; 25.445
90; 90.254; 90
1234.3Komkov, Alexander V.; Komendantova, Anna S.; Menchikov, Leonid G.; Chernoburova, Elena I.; Volkova, Yulia A.; Zavarzin, Igor V.
A Straightforward Approach toward Multifunctionalized Pyridazines via Imination/Electrocyclization.
Organic letters, 2015, 17, 3734-3737
1529882 CIFC27 H19 F3 N2P 1 21/c 17.4962; 17.6328; 16.4671
90; 93.865; 90
2171.65Cheng, Guolin; Weng, Yunxiang; Yang, Xifa; Cui, Xiuling
Base-Promoted N-Pyridylation of Heteroarenes Using N-Propargyl Enaminones as Equivalents of Pyridine Scaffolds.
Organic letters, 2015, 17, 3790-3793
1529883 CIFC19 H17 N O2P 21 21 217.3862; 11.9598; 17.2782
90; 90; 90
1526.31Cheng, Guolin; Weng, Yunxiang; Yang, Xifa; Cui, Xiuling
Base-Promoted N-Pyridylation of Heteroarenes Using N-Propargyl Enaminones as Equivalents of Pyridine Scaffolds.
Organic letters, 2015, 17, 3790-3793
1529884 CIFC26 H20 N2C 1 2/c 121.3348; 10.673; 18.3612
90; 110.777; 90
3909.1Cheng, Guolin; Weng, Yunxiang; Yang, Xifa; Cui, Xiuling
Base-Promoted N-Pyridylation of Heteroarenes Using N-Propargyl Enaminones as Equivalents of Pyridine Scaffolds.
Organic letters, 2015, 17, 3790-3793
1529885 CIFC32 H22 N6P 1 21/c 113.4407; 21.762; 8.4346
90; 99.174; 90
2435.5Constantinides, Christos P.; Zissimou, Georgia A.; Berezin, Andrey A.; Ioannou, Theodosia A.; Manoli, Maria; Tsokkou, Demetra; Theodorou, Eleni; Hayes, Sophia C.; Koutentis, Panayiotis A.
Tetraphenylhexaazaanthracenes: 16π Weakly Antiaromatic Species with Singlet Ground States.
Organic letters, 2015, 17, 4026-4029
1529886 CIFC28 H24 F3 N O4 SP -110.2147; 11.39; 12.1881
68.285; 71.067; 83.51
1246.1Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun
Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes.
Organic letters, 2015, 17, 3944-3947
1529887 CIFC12 H30 N2 O8 P2P 1 21/c 113.079; 9.117; 8.934
90; 107.82; 90
1014.2Li, Yufeng; Jian, Fangfang
Molecular Structures of the Products of a Diphosphonate Ester Building Block with Lewis Bases.
Molecules (Basel, Switzerland), 2015, 20, 14435-14450
1529888 CIFC12 H18 Na2 O12 P2P n m a8.201; 28.502; 9.712
90; 90; 90
2270.1Li, Yufeng; Jian, Fangfang
Molecular Structures of the Products of a Diphosphonate Ester Building Block with Lewis Bases.
Molecules (Basel, Switzerland), 2015, 20, 14435-14450
1529889 CIFC12 H16 O6 P2C 1 2/m 113.431; 8.8309; 7.781
90; 123.98; 90
765.3Li, Yufeng; Jian, Fangfang
Molecular Structures of the Products of a Diphosphonate Ester Building Block with Lewis Bases.
Molecules (Basel, Switzerland), 2015, 20, 14435-14450
1529890 CIFC18 H40 N2 O10 P2P -19.352; 10.458; 15.736
81.56; 82.84; 63.46
1358.9Li, Yufeng; Jian, Fangfang
Molecular Structures of the Products of a Diphosphonate Ester Building Block with Lewis Bases.
Molecules (Basel, Switzerland), 2015, 20, 14435-14450
1530387 CIFC32 H59 N O4 Si2P 1 21 116.472; 18.563; 11.996
90; 92.581; 90
3664.3Fanelli, Roberto; Salah, Khoubaib Ben Haj; Inguimbert, Nicolas; Didierjean, Claude; Martinez, Jean; Cavelier, Florine
Access to α,α-Disubstituted Disilylated Amino Acids and Their Use in Solid-Phase Peptide Synthesis.
Organic letters, 2015, 17, 4498-4501
1530388 CIFC22 H22 N2 O3 SP 1 21/n 113.4257; 10.9838; 14.5635
90; 109.954; 90
2018.7Wang, Chen; Zhang, Haojie; Lang, Bo; Ren, Anni; Lu, Ping; Wang, Yanguang
Rh-Catalyzed Reactions of 3-Diazoindolin-2-imines: Synthesis of Pyridoindoles and Tetrahydrofuropyrroloindoles.
Organic letters, 2015, 17, 4412-4415
1530389 CIFC17 H16 N2 OP 1 21/n 17.6543; 11.1582; 16.8881
90; 101.198; 90
1414.9Wang, Chen; Zhang, Haojie; Lang, Bo; Ren, Anni; Lu, Ping; Wang, Yanguang
Rh-Catalyzed Reactions of 3-Diazoindolin-2-imines: Synthesis of Pyridoindoles and Tetrahydrofuropyrroloindoles.
Organic letters, 2015, 17, 4412-4415
1530390 CIFC29 H44 O4P 21 21 217.3491; 11.3041; 30.6417
90; 90; 90
2545.56Hu, Zheng-Xi; Shi, Yi-Ming; Wang, Wei-Guang; Li, Xiao-Nian; Du, Xue; Liu, Miao; Li, Yan; Xue, Yong-Bo; Zhang, Yong-Hui; Pu, Jian-Xin; Sun, Han-Dong
Kadcoccinones A-F, New Biogenetically Related Lanostane-Type Triterpenoids with Diverse Skeletons from Kadsura coccinea.
Organic letters, 2015, 17, 4616-4619
1530391 CIFC32 H48 O5P 1 21 17.3331; 10.1624; 19.3573
90; 97.23; 90
1431.07Hu, Zheng-Xi; Shi, Yi-Ming; Wang, Wei-Guang; Li, Xiao-Nian; Du, Xue; Liu, Miao; Li, Yan; Xue, Yong-Bo; Zhang, Yong-Hui; Pu, Jian-Xin; Sun, Han-Dong
Kadcoccinones A-F, New Biogenetically Related Lanostane-Type Triterpenoids with Diverse Skeletons from Kadsura coccinea.
Organic letters, 2015, 17, 4616-4619
1530392 CIFC29 H44 O4P 17.357; 11.5004; 15.8083
101.789; 102.383; 90.228
1277.24Hu, Zheng-Xi; Shi, Yi-Ming; Wang, Wei-Guang; Li, Xiao-Nian; Du, Xue; Liu, Miao; Li, Yan; Xue, Yong-Bo; Zhang, Yong-Hui; Pu, Jian-Xin; Sun, Han-Dong
Kadcoccinones A-F, New Biogenetically Related Lanostane-Type Triterpenoids with Diverse Skeletons from Kadsura coccinea.
Organic letters, 2015, 17, 4616-4619
1530393 CIFC34 H54 O6P 1 21 17.9562; 33.6801; 12.617
90; 107.429; 90
3225.7Hu, Zheng-Xi; Shi, Yi-Ming; Wang, Wei-Guang; Li, Xiao-Nian; Du, Xue; Liu, Miao; Li, Yan; Xue, Yong-Bo; Zhang, Yong-Hui; Pu, Jian-Xin; Sun, Han-Dong
Kadcoccinones A-F, New Biogenetically Related Lanostane-Type Triterpenoids with Diverse Skeletons from Kadsura coccinea.
Organic letters, 2015, 17, 4616-4619
1530394 CIFC273 H261 Cl14 N O4P 1 21/n 116.1937; 43.708; 33.799
90; 92.7924; 90
23894Golling, Florian E.; Osella, Silvio; Quernheim, Martin; Wagner, Manfred; Beljonne, David; Müllen, Klaus
π-extended [12]cycloparaphenylenes: from a hexaphenylbenzene cyclohexamer to its unexpected C2-symmetric congener
Chem. Sci., 2015, 6, 7072
1530395 CIFC46 H52 Br2P 1 21/c 112.9767; 10.3514; 15.6662
90; 105.739; 90
2025.5Golling, Florian E.; Osella, Silvio; Quernheim, Martin; Wagner, Manfred; Beljonne, David; Müllen, Klaus
π-extended [12]cycloparaphenylenes: from a hexaphenylbenzene cyclohexamer to its unexpected C2-symmetric congener
Chem. Sci., 2015, 6, 7072
1530396 CIFC14 H30 Cl4 N4 Ni O4P c a 2112.3629; 12.8888; 13.1011
90; 90; 90
2087.6Marriott, Katie E. R.; Bhaskaran, Lakshmi; Wilson, Claire; Medarde, Marisa; Ochsenbein, Stefan T.; Hill, Stephen; Murrie, Mark
Pushing the limits of magnetic anisotropy in trigonal bipyramidal Ni(ii)
Chem. Sci., 2015, 6, 6823
1530397 CIFC59 H99 Co3 Fe2 N21 O22C 1 2/c 126.362; 16.67; 19.521
90; 108.29; 90
8145Pan, F.; Gao, S.; Liu, H. Z.
A heterometallic nanosized tube {Fe[(CN)6]2[Co(LN3O2)]3}nand two of its lamellar polymorphous isomers
CrystEngComm, 2015, 17, 7490
1530398 CIFC114 H164 Co6 Fe4 N42 O31P 1 21/c 117.276; 29.697; 31.436
90; 98.5; 90
15951Pan, F.; Gao, S.; Liu, H. Z.
A heterometallic nanosized tube {Fe[(CN)6]2[Co(LN3O2)]3}nand two of its lamellar polymorphous isomers
CrystEngComm, 2015, 17, 7490
1530399 CIFC57 H75 Co3 Fe2 N21 O12P 1 21/n 110.187; 42.792; 17.083
90; 101.5; 90
7297Pan, F.; Gao, S.; Liu, H. Z.
A heterometallic nanosized tube {Fe[(CN)6]2[Co(LN3O2)]3}nand two of its lamellar polymorphous isomers
CrystEngComm, 2015, 17, 7490
1530687 CIFC26 H40 O9P 21 21 217.9069; 8.1826; 38.9732
90; 90; 90
2521.53Huang, Zheng; Zhu, Zhi-Xiang; Li, Yue-Ting; Pang, Dao-Ran; Zheng, Jiao; Zhang, Qian; Zhao, Yun-Fang; Ferreira, Daneel; Zjawiony, Jordan K.; Tu, Peng-Fei; Li, Jun
Anti-inflammatory Labdane Diterpenoids from Leonurus macranthus.
Journal of natural products, 2015, 78, 2276-2285
1530688 CIFC36 H53 N3 O4 SP 1 2 120.4743; 8.7109; 22.4995
90; 112.422; 90
3709.4Martinot, Theodore A.; Austad, Brian C.; Côté, Alexandre; Depew, Kristopher M.; Genov, Daniel; Grenier, Louis; Helble, Joseph; Lescarbeau, Andre; Nair, Somarajan; Trudeau, Martin; White, Priscilla; Yu, Lin-Chen
A Design of Experiments Approach to a Robust Final Deprotection and Reactive Crystallization of IPI-926, A Novel Hedgehog Pathway Inhibitor
Organic Process Research & Development, 2015, 19, 1693
1530689 CIFC29 H49 Cl N2 O3 SP 6121.0551; 21.0551; 13.925
90; 90; 120
5346.1Martinot, Theodore A.; Austad, Brian C.; Côté, Alexandre; Depew, Kristopher M.; Genov, Daniel; Grenier, Louis; Helble, Joseph; Lescarbeau, Andre; Nair, Somarajan; Trudeau, Martin; White, Priscilla; Yu, Lin-Chen
A Design of Experiments Approach to a Robust Final Deprotection and Reactive Crystallization of IPI-926, A Novel Hedgehog Pathway Inhibitor
Organic Process Research & Development, 2015, 19, 1693
1530690 CIFC38 H60.5 Br N2 O5.25 S2P 1 21 17.378; 14.3067; 36.57
90; 92.36; 90
3856.9Martinot, Theodore A.; Austad, Brian C.; Côté, Alexandre; Depew, Kristopher M.; Genov, Daniel; Grenier, Louis; Helble, Joseph; Lescarbeau, Andre; Nair, Somarajan; Trudeau, Martin; White, Priscilla; Yu, Lin-Chen
A Design of Experiments Approach to a Robust Final Deprotection and Reactive Crystallization of IPI-926, A Novel Hedgehog Pathway Inhibitor
Organic Process Research & Development, 2015, 19, 1693
1530691 CIFC42 H52 Cl Co N4P 1 21/c 123.591; 10.436; 15.7392
90; 101.118; 90
3802.2Meng, Yin-Shan; Mo, Zhenbo; Wang, Bing-Wu; Zhang, Yi-Quan; Deng, Liang; Gao, Song
Observation of the single-ion magnet behavior of d8ions on two-coordinate Co(i)‒NHC complexes
Chem. Sci., 2015, 6, 7156
1530692 CIFC66 H72 B Co N4C 1 2/c 129.581; 11.9267; 32.317
90; 101.11; 90
11187.9Meng, Yin-Shan; Mo, Zhenbo; Wang, Bing-Wu; Zhang, Yi-Quan; Deng, Liang; Gao, Song
Observation of the single-ion magnet behavior of d8ions on two-coordinate Co(i)‒NHC complexes
Chem. Sci., 2015, 6, 7156
1530693 CIFC78 H76 B Co F24 N4P 42/n :214.0529; 14.0529; 18.2643
90; 90; 90
3606.9Meng, Yin-Shan; Mo, Zhenbo; Wang, Bing-Wu; Zhang, Yi-Quan; Deng, Liang; Gao, Song
Observation of the single-ion magnet behavior of d8ions on two-coordinate Co(i)‒NHC complexes
Chem. Sci., 2015, 6, 7156
1530694 CIFC11 H7 Fe2 N O6 S2P -19.127; 9.176; 10.453
102.454; 105.352; 97.467
807.9Tooley, C. A.; Pazicni, S.; Berda, E. B.
Toward a tunable synthetic [FeFe] hydrogenase mimic: single-chain nanoparticles functionalized with a single diiron cluster
Polym. Chem., 2015, 6, 7646
1530695 CIFC11 H9 Fe2 N O6 S2P 1 21/n 16.8072; 18.152; 13.3181
90; 90.497; 90
1645.6Tooley, C. A.; Pazicni, S.; Berda, E. B.
Toward a tunable synthetic [FeFe] hydrogenase mimic: single-chain nanoparticles functionalized with a single diiron cluster
Polym. Chem., 2015, 6, 7646
1530696 CIFC27 H21 N1.5 O6 P1.5C 1 2 118.901; 7.5595; 17.833
90; 111.235; 90
2375Abbassi, Leïla; Chabre, Yoann M.; Kottari, Naresh; Arnold, Alexandre A.; André, Sabine; Josserand, Johan; Gabius, Hans-Joachim; Roy, René
Multifaceted glycodendrimers with programmable bioactivity through convergent, divergent, and accelerated approaches using polyfunctional cyclotriphosphazenes
Polym. Chem., 2015, 6, 7666
1531034 CIFC23 H22 N2 O5P 1 21/c 110.82123; 22.8438; 8.59627
90; 108.437; 90
2015.91Zhan, Gu; Shi, Ming-Lin; He, Qing; Du, Wei; Chen, Ying-Chun
[4 + 3] Cycloadditions with Bromo-Substituted Morita-Baylis-Hillman Adducts of Isatins and N-(ortho-Chloromethyl)aryl Amides.
Organic letters, 2015, 17, 4750-4753
1531035 CIFC93 H37 Cu F35 N14P -116.017; 18.231; 18.359
115.519; 101.669; 92.884
4680.3Zhang, Kai; Zhang, Junda; Li, Xin; Guo, Rui; Ågren, Hans; Ou, Zhongping; Ishida, Masatoshi; Furuta, Hiroyuki; Xie, Yongshu
Synthesis of a Neo-Confused Octaphyrin and the Formation of Its Mononuclear Complexes.
Organic letters, 2015, 17, 4806-4809
1531036 CIFC89 H31 F35 N12 ZnP -116.045; 18.292; 18.495
115.633; 101.728; 93.013
4730.7Zhang, Kai; Zhang, Junda; Li, Xin; Guo, Rui; Ågren, Hans; Ou, Zhongping; Ishida, Masatoshi; Furuta, Hiroyuki; Xie, Yongshu
Synthesis of a Neo-Confused Octaphyrin and the Formation of Its Mononuclear Complexes.
Organic letters, 2015, 17, 4806-4809
1531037 CIFC180 H48 O32 Zr6F m -3 m45.887; 45.887; 45.887
90; 90; 90
96620Sawano, Takahiro; Ji, Pengfei; McIsaac, Alexandra R.; Lin, Zekai; Abney, Carter W.; Lin, Wenbin
The first chiral diene-based metal‒organic frameworks for highly enantioselective carbon‒carbon bond formation reactions
Chem. Sci., 2015, 6, 7163
1531038 CIFC107 H168 Fe2 N14 P2 Si6P -111.5288; 12.5203; 21.155
73.555; 75.604; 74.65
2774Metsänen, Toni T.; Gallego, Daniel; Szilvási, Tibor; Driess, Matthias; Oestreich, Martin
Peripheral mechanism of a carbonyl hydrosilylation catalysed by an SiNSi iron pincer complex
Chem. Sci., 2015, 6, 7143
1531040 CIFC16 H16 F N2 O5 VP 1 21/c 17.9908; 17.1771; 11.9692
90; 100.208; 90
1616.87Gazi, Sarifuddin; Hung Ng, Wilson Kwok; Ganguly, Rakesh; Putra Moeljadi, Adhitya Mangala; Hirao, Hajime; Soo, Han Sen
Selective photocatalytic C‒C bond cleavage under ambient conditions with earth abundant vanadium complexes
Chem. Sci., 2015, 6, 7130
1531041 CIFC30 H44 N2 O8 V2C 1 2/c 112.1706; 11.0345; 23.8844
90; 100.883; 90
3149.9Gazi, Sarifuddin; Hung Ng, Wilson Kwok; Ganguly, Rakesh; Putra Moeljadi, Adhitya Mangala; Hirao, Hajime; Soo, Han Sen
Selective photocatalytic C‒C bond cleavage under ambient conditions with earth abundant vanadium complexes
Chem. Sci., 2015, 6, 7130
1531042 CIFC15 H22 N O4 VP n a 2114.7897; 13.1867; 7.8841
90; 90; 90
1537.62Gazi, Sarifuddin; Hung Ng, Wilson Kwok; Ganguly, Rakesh; Putra Moeljadi, Adhitya Mangala; Hirao, Hajime; Soo, Han Sen
Selective photocatalytic C‒C bond cleavage under ambient conditions with earth abundant vanadium complexes
Chem. Sci., 2015, 6, 7130
1531043 CIFC19 H16 O7P 1 21/c 114.7352; 8.7127; 14.2158
90; 114.431; 90
1661.7Ma, Yan-Yan; Zhao, Deng-Gao; Zhou, Ai-Yu; Zhang, Yu; Du, Zhiyun; Zhang, Kun
α-Glucosidase Inhibition and Antihyperglycemic Activity of Phenolics from the Flowers of Edgeworthia gardneri.
Journal of agricultural and food chemistry, 2015, 63, 8162-8169
1531044 CIFC30 H22 O4P 1 21 17.0717; 8.8439; 19.5443
90; 96.556; 90
1214.33Wang, De; Wang, Guo-Peng; Sun, Yao-Liang; Zhu, Shou-Fei; Wei, Yin; Zhou, Qi-Lin; Shi, Min
Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones
Chem. Sci., 2015, 6, 7319
1531045 CIFC38.5 H29 Cl O4C 1 2 116.8074; 10.9989; 16.649
90; 92.018; 90
3075.9Wang, De; Wang, Guo-Peng; Sun, Yao-Liang; Zhu, Shou-Fei; Wei, Yin; Zhou, Qi-Lin; Shi, Min
Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones
Chem. Sci., 2015, 6, 7319
1531046 CIFC27 H23 N O4P 1 21 18.1626; 12.2302; 11.0742
90; 101.402; 90
1083.72Wang, De; Wang, Guo-Peng; Sun, Yao-Liang; Zhu, Shou-Fei; Wei, Yin; Zhou, Qi-Lin; Shi, Min
Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones
Chem. Sci., 2015, 6, 7319
1531047 CIFC30 H21 F3 N2C 1 2/c 128.3793; 8.2635; 21.2253
90; 112.455; 90
4600.2Mukundam, Vanga; Kumar, Atul; Dhanunjayarao, Kunchala; Ravi, Arthi; Peruncheralathan, S.; Venkatasubbaiah, Krishnan
Tetraaryl pyrazole polymers: versatile synthesis, aggregation induced emission enhancement and detection of explosives
Polym. Chem., 2015, 6, 7764
1531166 CIFC28 H26 N2 O4 S2P -19.2332; 11.8033; 13.4383
78.564; 74.091; 80.538
1371.04Hou, Wenduan; Wei, Qi; Liu, Guisheng; Chen, Jing; Guo, Jing; Peng, Yungui
Asymmetric Multicomponent Sulfa-Michael/Mannich Cascade Reaction: Synthetic Access to 1,2-Diamino-3-Organosulfur Compounds and 2-Nitro Allylic Amines.
Organic letters, 2015, 17, 4870-4873
1531170 CIFC28 H26 N2 O4 S2P 21 21 217.8395; 12.02537; 26.9644
90; 90; 90
2542.01Hou, Wenduan; Wei, Qi; Liu, Guisheng; Chen, Jing; Guo, Jing; Peng, Yungui
Asymmetric Multicomponent Sulfa-Michael/Mannich Cascade Reaction: Synthetic Access to 1,2-Diamino-3-Organosulfur Compounds and 2-Nitro Allylic Amines.
Organic letters, 2015, 17, 4870-4873
1531174 CIFC28 H26 N2 O4 S2P 21 21 215.35547; 17.35361; 27.184
90; 90; 90
2526.39Hou, Wenduan; Wei, Qi; Liu, Guisheng; Chen, Jing; Guo, Jing; Peng, Yungui
Asymmetric Multicomponent Sulfa-Michael/Mannich Cascade Reaction: Synthetic Access to 1,2-Diamino-3-Organosulfur Compounds and 2-Nitro Allylic Amines.
Organic letters, 2015, 17, 4870-4873
1531311 CIFC60 H79 B N3 O2 Sc SiP -112.489; 12.502; 20.618
84.375; 75.312; 65.747
2839.1Wang, Baoli; Kang, Xiaohui; Nishiura, Masayoshi; Luo, Yi; Hou, Zhaomin
Isolation, structure and reactivity of a scandium boryl oxycarbene complex
Chem. Sci., 2015
1531312 CIFC54 H81 B N3 O2 Sc SiP 1 21/n 113.706; 12.501; 31.255
90; 97.34; 90
5311Wang, Baoli; Kang, Xiaohui; Nishiura, Masayoshi; Luo, Yi; Hou, Zhaomin
Isolation, structure and reactivity of a scandium boryl oxycarbene complex
Chem. Sci., 2015
1531313 CIFC53 H75 B N3 O4 Sc SiP -112.0903; 12.7458; 18.106
93.545; 99.571; 114.287
2481.3Wang, Baoli; Kang, Xiaohui; Nishiura, Masayoshi; Luo, Yi; Hou, Zhaomin
Isolation, structure and reactivity of a scandium boryl oxycarbene complex
Chem. Sci., 2015
1531314 CIFC59 H79 B N4 O Sc SiP -112.7148; 14.2837; 15.4973
102.293; 99.228; 91.066
2710.3Wang, Baoli; Kang, Xiaohui; Nishiura, Masayoshi; Luo, Yi; Hou, Zhaomin
Isolation, structure and reactivity of a scandium boryl oxycarbene complex
Chem. Sci., 2015
1531315 CIFC50 H71 B N3 O2 Sc SiP 1 21/c 112.8438; 20.755; 18.74
90; 108.462; 90
4738.5Wang, Baoli; Kang, Xiaohui; Nishiura, Masayoshi; Luo, Yi; Hou, Zhaomin
Isolation, structure and reactivity of a scandium boryl oxycarbene complex
Chem. Sci., 2015
1531316 CIFC24 H17 N OP 1 21/n 112.9997; 21.3361; 13.502
90; 106.398; 90
3592.6Poudel, Tej Narayan; Lee, Yong Rok
Construction of highly functionalized carbazoles via condensation of an enolate to a nitro group
Chem. Sci., 2015, 6, 7028
1531795 CIFC22 H26 O9P 1 21 16.58475; 12.3394; 13.1873
90; 101.317; 90
1050.66Wang, Yuezhou; Qi, Shuang; Zhan, Ying; Zhang, Nanwen; Wu, An-An; Gui, Fu; Guo, Kai; Yang, Yanru; Cao, Shugeng; Hu, Zhiyu; Zheng, Zhonghui; Song, Siyang; Xu, Qingyan; Shen, Yuemao; Deng, Xianming
Aspertetranones A-D, Putative Meroterpenoids from the Marine Algal-Associated Fungus Aspergillus sp. ZL0-1b14.
Journal of natural products, 2015, 78, 2405-2410
1531937 CIFC98 H96 B F24 N2 O Pd TlP -112.7422; 26.6786; 28.5026
99.098; 90.144; 90.509
9566.9Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531938 CIFC108 H102 B F24 N2 Pd TlP -112.5519; 20.2591; 21.647
105.597; 102.325; 97.308
5079.1Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531939 CIFC152 H172 Ag4 F12 N4 O12 Pt2 S4P 1 21/n 111.7798; 29.62; 20.9358
90; 90.39; 90
7304.7Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531940 CIFC81 H92 Ag F3 N2 O3 Pt SP 1 21/n 118.6061; 19.7722; 20.9507
90; 106.515; 90
7389.5Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531941 CIFC71 H94 F3 N2 O5 Pt S TlP -113.95; 16.2777; 17.6213
66.887; 70.018; 71.465
3379.6Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531942 CIFC93 H134 Ag F3 N2 O10.5 Pd SP 21 21 2115.5936; 21.315; 24.141
90; 90; 90
8023.9Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531943 CIFC79 H106 Ag F3 N5 O4 Pt SP 21 21 2115.6478; 21.2503; 24.077
90; 90; 90
8006.1Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531944 CIFC84 H98 Ag F3 N2 O3 Pd SP -114.5289; 15.663; 17.673
96.662; 109.412; 94.019
3742.1Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531945 CIFC98 H96 B F24 N2 O Pt TlP -112.7326; 26.642; 28.428
99.2; 90.224; 90.514
9518.8Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531946 CIFC94 H86 B F24 N2 Pt TlP -114.6265; 20.6542; 31.1986
76.597; 79.378; 89.566
9005.2Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531947 CIFC3 H7 Cl3 I0 N O0 PbP 43 21 210.4482; 10.4482; 14.7573
90; 90; 90
1611Wang, Guan-E; Xu, Gang; Wang, Ming-Sheng; Cai, Li-Zhen; Li, Wen-Hua; Guo, Guo-Cong
Semiconductive 3-D haloplumbate framework hybrids with high color rendering index white-light emission
Chem. Sci., 2015, 6, 7222
1531948 CIFC80 H180 Cl59 N16 O2 Pb21P 1 21/c 121.2016; 15.9211; 26.4092
90; 91.811; 90
8910Wang, Guan-E; Xu, Gang; Wang, Ming-Sheng; Cai, Li-Zhen; Li, Wen-Hua; Guo, Guo-Cong
Semiconductive 3-D haloplumbate framework hybrids with high color rendering index white-light emission
Chem. Sci., 2015, 6, 7222
1532146 CIFC24 H12 N6 O6P b c n7.235; 41.244; 21.816
90; 90; 90
6510Zhan, Tian-Guang; Zhou, Tian-You; Qi, Qiao-Yan; Wu, Jian; Li, Guang-Yu; Zhao, Xin
The construction of supramolecular polymers through anion bridging: from frustrated hydrogen-bonding networks to well-ordered linear arrays
Polym. Chem., 2015, 6, 7586
1532452 CIFC15 H34 I2 N4 Ni O4 S2P -110.141; 11.619; 11.643
86.263; 69.71; 76.551
1251.3Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y.
The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes
Chem. Sci., 2015, 6, 7079
1532453 CIFC15 H29 Co N2 O6 S2P -17.5419; 8.0477; 16.687
78.174; 82.069; 86.421
981.2Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y.
The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes
Chem. Sci., 2015, 6, 7079
1532454 CIFC15 H28 Fe N2 O6 S2P -17.486; 8.04; 16.74
78.165; 82.235; 86.603
976.6Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y.
The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes
Chem. Sci., 2015, 6, 7079
1532455 CIFC30 H56 Cu2 N4 O12 S4C 1 2/c 119.683; 12.1661; 19.517
90; 106.346; 90
4484.7Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y.
The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes
Chem. Sci., 2015, 6, 7079
1532456 CIFC11 H24 N2 O2 S2P 1 21/c 19.6252; 12.3461; 12.2335
90; 103.606; 90
1413Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y.
The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes
Chem. Sci., 2015, 6, 7079
1532457 CIFC32 H40 S3P -19.799; 11.932; 13.735
84.22; 72.85; 66.98
1412.1Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji
Synthesis and Properties of Ethene-Bridged Terthiophenes.
Organic letters, 2015, 17, 4858-4861
1532458 CIFC32 H40 S3P -110.274; 10.828; 13.62
73.61; 83.52; 85.57
1443Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji
Synthesis and Properties of Ethene-Bridged Terthiophenes.
Organic letters, 2015, 17, 4858-4861
1532459 CIFC28 H32 S3P -17.769; 12.591; 12.753
93.524; 98.169; 101.228
1206.1Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji
Synthesis and Properties of Ethene-Bridged Terthiophenes.
Organic letters, 2015, 17, 4858-4861
1532460 CIFC24 H24 S3P 1 21/c 111.959; 22.114; 7.632
90; 97.436; 90
2001Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji
Synthesis and Properties of Ethene-Bridged Terthiophenes.
Organic letters, 2015, 17, 4858-4861
1532461 CIFC16 H8 S3P 1 21/c 113.033; 3.916; 24.464
90; 103.214; 90
1215.5Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji
Synthesis and Properties of Ethene-Bridged Terthiophenes.
Organic letters, 2015, 17, 4858-4861
1532465 CIFC47.5 H62.5 F6 N1.5 O6.5 PP 1 2/c 115.9874; 18.0758; 18.1871
90; 107.85; 90
5002.8Jia, Fei; He, Zhenfeng; Yang, Liu-Pan; Pan, Zhi-Sheng; Yi, Min; Jiang, Ren-Wang; Jiang, Wei
Oxatub[4]arene: a smart macrocyclic receptor with multiple interconvertible cavities
Chem. Sci., 2015, 6, 6731
1532466 CIFC138 H129 F18 N3 O18 P3R -3 :H43.2165; 43.2165; 12.4664
90; 90; 120
20163.7Jia, Fei; He, Zhenfeng; Yang, Liu-Pan; Pan, Zhi-Sheng; Yi, Min; Jiang, Ren-Wang; Jiang, Wei
Oxatub[4]arene: a smart macrocyclic receptor with multiple interconvertible cavities
Chem. Sci., 2015, 6, 6731
1532468 CIFC82 H116 Cd2 N24 O25C 1 2/c 130.664; 17.225; 27.371
90; 105.9; 90
13904Sun, Chun-Yi; To, Wai-Pong; Wang, Xin-Long; Chan, Kaai-Tung; Su, Zhong-Min; Che, Chi-Ming
Metal‒organic framework composites with luminescent gold(iii) complexes. Strongly emissive and long-lived excited states in open air and photo-catalysis
Chem. Sci., 2015, 6, 7105
1532469 CIFC91.5 H111.5 Ge2 N2 Si2P -110.806; 18.897; 21.557
108.61; 90.43; 103.93
4032.1Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532470 CIFC104 H122 Ge2 N2 O2 Si2P 1 21/n 113.373; 21.643; 15.884
90; 102.62; 90
4486.3Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532471 CIFC46 H57 Ge N SiP -110.783; 11.465; 16.298
97.01; 91.76; 92.77
1996.1Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532472 CIFC52 H61 Ge N SiP 1 21/n 111.543; 23.7164; 16.3022
90; 97.979; 90
4419.7Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532473 CIFC49 H61 Ge N SiP 1 21/c 110.319; 18.286; 22.437
90; 91.27; 90
4232.7Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532474 CIFC50 H63 Ge N SiP 1 21 110.2741; 14.6818; 14.6417
90; 102.077; 90
2159.71Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532475 CIFC52 H67 Ge N SiP 1 21/n 19.942; 15.413; 28.793
90; 97.18; 90
4377.5Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532476 CIFC46 H57 N Si SnP -110.673; 12.534; 15.493
82.27; 85.09; 73.63
1968Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532477 CIFC52 H68 N Si SnP -110.2591; 13.6505; 17.3164
99.111; 105.293; 95.189
2287.3Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532478 CIFC53 H61 Ge N SiP 1 21/n 110.0813; 15.796; 28.096
90; 96.916; 90
4441.6Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532479 CIFC53 H61 N Si SnP 1 21/n 110.1088; 15.7379; 28.106
90; 96.853; 90
4439.5Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532480 CIFC52 H65 Ge N SiP 1 21/n 110.003; 15.4017; 28.92
90; 97.698; 90
4415.4Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532481 CIFC49 H63 Ge N SiP 1 21/n 111.374; 23.3065; 16.3439
90; 97.891; 90
4291.5Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532482 CIFC49 H62 Cl Ge N SiP -110.731; 14.446; 15.647
77.83; 78.54; 69.06
2194.2Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532483 CIFC48 H63 Ge N O SiP -110.399; 14.2109; 15.4524
90.483; 101.026; 105.118
2159.72Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532484 CIFC53 H70 N2 O Si SnP -114.604; 15.84; 20.773
88.61; 82.84; 84.99
4749.2Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532485 CIFC112 H154 Ge2 N2 O2 Si2P 1 21/n 115.0392; 12.4994; 26.2128
90; 93.127; 90
4920.17Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532486 CIFC112 H158 N2 O2 Si2 Sn2P -115.4827; 16.4448; 23.7823
72.311; 88.259; 62.908
5094.1Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532487 CIFC23 H32 O7P 21 21 219.772; 13.5369; 16.5519
90; 90; 90
2189.53Ma, Guoxu; Wu, Haifeng; Chen, Deli; Zhu, Nailiang; Zhu, Yindi; Sun, Zhonghao; Li, Pengfei; Yang, Junshan; Yuan, Jingquan; Xu, Xudong
Antimalarial and Antiproliferative Cassane Diterpenes of Caesalpinia sappan.
Journal of natural products, 2015, 78, 2364-2371
1532490 CIFC27 H30 B2 D3 N2 O2P -16.2435; 13.8921; 14.2338
100.533; 92.139; 100.164
1191.63Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei
Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene
Chem. Sci., 2015, 6, 7150
1532491 CIFC30 H34 B2 N2 O2P -112.0335; 13.357; 17.045
73.663; 81.968; 79.686
2575Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei
Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene
Chem. Sci., 2015, 6, 7150
1532492 CIFC31 H36 B2 N2 O2P 1 21/n 19.498; 9.09; 30.647
90; 94.119; 90
2639.1Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei
Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene
Chem. Sci., 2015, 6, 7150
1532493 CIFC30 H33 B2 Br N2 O2P 1 21/n 19.5066; 9.248; 30.632
90; 94.399; 90
2685.1Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei
Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene
Chem. Sci., 2015, 6, 7150
1532494 CIFC32 H39 B2 N2 O2P 1 21/n 18.8862; 21.985; 14.0495
90; 96.2349; 90
2728.5Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei
Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene
Chem. Sci., 2015, 6, 7150
1532495 CIFC33 H52 I P2 PdP b c a14.978; 16.438; 29.361
90; 90; 90
7229Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532496 CIFC65 H64 B F24 I P2 PdP 1 21/n 114.0602; 28.6171; 16.9031
90; 92.0331; 90
6796.9Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532497 CIFC33 H53 I P2 PdP 1 21/c 112.8203; 14.834; 19.174
90; 106.641; 90
3493.7Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532498 CIFC40 H60 I N P2 PdP 1 21/n 117.0891; 14.014; 18.4206
90; 100.081; 90
4343.4Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532499 CIFC39 H57 I O P2 PdP -111.8764; 14.433; 25.1741
101.297; 93.5784; 111.2
3903Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532500 CIFC68 H72 B F24 I P3 PdP 1 21 110.0901; 23.7955; 31.205
90; 90.532; 90
7492Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532501 CIFC44 H67 F3 O4 P2 Pd S2P 21 21 2114.0266; 15.2323; 21.3735
90; 90; 90
4566.6Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532502 CIFC50 H74 P2 Pd S2P 1 21/n 111.297; 11.59; 36.768
90; 92.926; 90
4808Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532507 CIFC8 H4 F S3P n m a7.784; 22.5821; 9.6099
90; 90; 90
1689.22Debnath, Sashi; Bedi, Anjan; Zade, Sanjio S.
Thienopentathiepine: a sulfur containing fused heterocycle for conjugated systems and their electrochemical polymerization
Polym. Chem., 2015, 6, 7658
1532508 CIFC16 H10 S6C 1 2/c 124.2039; 6.2548; 22.525
90; 103.733; 90
3312.6Debnath, Sashi; Bedi, Anjan; Zade, Sanjio S.
Thienopentathiepine: a sulfur containing fused heterocycle for conjugated systems and their electrochemical polymerization
Polym. Chem., 2015, 6, 7658
1532509 CIFC12 H6 S6 Se2P b c a16.5074; 8.21747; 23.5969
90; 90; 90
3200.9Debnath, Sashi; Bedi, Anjan; Zade, Sanjio S.
Thienopentathiepine: a sulfur containing fused heterocycle for conjugated systems and their electrochemical polymerization
Polym. Chem., 2015, 6, 7658
1532510 CIFC12 H6 S8P 1 21/c 18.3161; 20.227; 9.2199
90; 92.391; 90
1549.53Debnath, Sashi; Bedi, Anjan; Zade, Sanjio S.
Thienopentathiepine: a sulfur containing fused heterocycle for conjugated systems and their electrochemical polymerization
Polym. Chem., 2015, 6, 7658
1532833 CIFC21 H28 N2 O4P 21 21 218.7278; 9.6635; 46.6791
90; 90; 90
3937Chung, John Y. L.; Marcune, Benjamin; Strotman, Hallena R.; Petrova, Rositza I.; Moore, Jeffrey C.; Dormer, Peter G.
Synthesis of ((3R,6R)-6-Methylpiperidin-3-yl)methanol via Biocatalytic Transamination and Crystallization-Induced Dynamic Resolution
Organic Process Research & Development, 2015, 19, 1418
1533007 CIFC75 H88 Mo4 O8 P2 Sm2P -19.5023; 12.6103; 15.1418
97.784; 90.79; 100.069
1768.68Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533008 CIFC68 H80 Mo4 O8 P2 Yb2P -19.4563; 12.5189; 14.9787
84.903; 71.669; 76.285
1635Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533009 CIFC68 H86 Mo2 O4 P4 Sm2P -19.6185; 10.2667; 17.5096
83.519; 77.307; 78.461
1648.4Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533010 CIFC81 H105 Mo3 O6 P5 Sm3P 1 21/m 110.13; 25.686; 15.724
90; 96.36; 90
4066.2Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533011 CIFC78 H106 Mo2 O4 P6 Sm2P -111.1671; 12.7931; 14.7276
98.952; 110.227; 95.319
1925.7Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533012 CIFC78 H106 Mo2 O4 P6 Yb2P -111.1924; 12.6285; 14.6371
99.581; 110.455; 94.847
1888.44Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533373 CIFC28 H42 Au Cl3 N4 OI 41/a37.1846; 37.1846; 9.743
90; 90; 90
13471.6Ramsay, William J.; Foster, Jonathan A.; Moore, Katharine L.; Ronson, Tanya K.; Mirgalet, Raphaël J.; Jefferson, David A.; Nitschke, Jonathan R.
AuICl-bound N-heterocyclic carbene ligands form MII4(LAuCl)6integrally gilded cages
Chem. Sci., 2015, 6, 7326
1533374 CIFC30 H33 Cl F3 Ir N2 O2P 1 21/n 111.3662; 17.1523; 15.528
90; 111.111; 90
2824.1Yellol, Jyoti; Pérez, Sergio A; Buceta, Alicia; Yellol, Gorakh; Donaire, Antonio; Szumlas, Piotr; Bednarski, Patrick J.; Makhloufi, Gamall; Janiak, Christoph; Espinosa, Arturo; Ruiz, José
Novel C,N-Cyclometalated Benzimidazole Ruthenium(II) and Iridium(III) Complexes as Antitumor and Antiangiogenic Agents: A Structure-Activity Relationship Study.
Journal of medicinal chemistry, 2015, 58, 7310-7327
1533375 CIFC30 H32 Cl F3 N2 O2 RuP 1 21/c 112.5656; 17.1429; 13.9971
90; 108.785; 90
2854.5Yellol, Jyoti; Pérez, Sergio A; Buceta, Alicia; Yellol, Gorakh; Donaire, Antonio; Szumlas, Piotr; Bednarski, Patrick J.; Makhloufi, Gamall; Janiak, Christoph; Espinosa, Arturo; Ruiz, José
Novel C,N-Cyclometalated Benzimidazole Ruthenium(II) and Iridium(III) Complexes as Antitumor and Antiangiogenic Agents: A Structure-Activity Relationship Study.
Journal of medicinal chemistry, 2015, 58, 7310-7327
1533376 CIFC25.5 H28 O12.5P 21 21 2115.0788; 17.5135; 19.2065
90; 90; 90
5072.1Gan, Maoluo; Liu, Bin; Tan, Yi; Wang, Qiang; Zhou, Hongxia; He, Hongwei; Ping, Yuhui; Yang, Zhaoyong; Wang, Yiguang; Xiao, Chunling
Saccharothrixones A-D, Tetracenomycin-Type Polyketides from the Marine-Derived Actinomycete Saccharothrix sp. 10-10.
Journal of natural products, 2015, 78, 2260-2265
1534094 CIFC79 H60 Cl2 N10 O7 RuP -112.6643; 15.7605; 18.076
105.968; 97.219; 99.105
3370.1Fan, Congbin; Ye, Changqing; Wang, Xiaomei; Chen, Zhigang; Zhou, Yuyang; Liang, Zuoqin; Tao, Xutang
Synthesis and Electrochromic Properties of New Terpyridine‒Triphenylamine Hybrid Polymers
Macromolecules, 2015, 48, 6465
1534095 CIFC32 H40 N0 O8P 21 21 218.2474; 12.543; 29.019
90; 90; 90
3001.9Yang, Shanshan; Sun, Jiachen; Lu, Hong; Ma, Hong; Zhang, Yaozhou
Bioactivity-guided isolation of anticancer compounds from Euphorbia lathyris
Anal. Methods, 2015, 7, 9568
1534096 CIFC16 H16 Br N O2P 21 21 215.1904; 9.7263; 29.581
90; 90; 90
1493.3Pathipati, Stalin R.; Singh, Vipender; Eriksson, Lars; Selander, Nicklas
Lewis Acid Catalyzed Annulation of Nitrones with Oxiranes, Aziridines, and Thiiranes.
Organic letters, 2015, 17, 4506-4509
1534097 CIFC27 H21 N O4P 1 21/c 111.7836; 8.1908; 21.1196
90; 92.216; 90
2036.9Jung, Youngeun; Kim, Ikyon
Deformylative Intramolecular Hydroarylation: Synthesis of Benzo[e]pyrido[1,2-a]indoles.
Organic letters, 2015, 17, 4600-4603
1534098 CIFC26 H21 N O3P 1 21/c 111.5406; 9.3427; 18.9135
90; 96.804; 90
2024.9Jung, Youngeun; Kim, Ikyon
Deformylative Intramolecular Hydroarylation: Synthesis of Benzo[e]pyrido[1,2-a]indoles.
Organic letters, 2015, 17, 4600-4603
1534099 CIFC62 H60 Cl N4 O4 PP 1 21 113.9954; 19.389; 14.02
90; 115.309; 90
3439.3Gao, Xing; Han, Jianwei; Wang, Limin
Design of Highly Stable Iminophosphoranes as Recyclable Organocatalysts: Application to Asymmetric Chlorinations of Oxindoles.
Organic letters, 2015, 17, 4596-4599
1534100 CIFC65 H65 N4 O5 PP 1 21 112.0658; 17.7295; 13.2309
90; 104.155; 90
2744.4Gao, Xing; Han, Jianwei; Wang, Limin
Design of Highly Stable Iminophosphoranes as Recyclable Organocatalysts: Application to Asymmetric Chlorinations of Oxindoles.
Organic letters, 2015, 17, 4596-4599
1534101 CIFC24 H29 F N2 O5R 3 :H31.82; 31.82; 6.203
90; 90; 120
5439.2Bonetti, Andrea; Pellegrino, Sara; Das, Priyadip; Yuran, Sivan; Bucci, Raffaella; Ferri, Nicola; Meneghetti, Fiorella; Castellano, Carlo; Reches, Meital; Gelmi, Maria Luisa
Dipeptide Nanotubes Containing Unnatural Fluorine-Substituted β(2,3)-Diarylamino Acid and l-Alanine as Candidates for Biomedical Applications.
Organic letters, 2015, 17, 4468-4471
1534102 CIFC15 H17 N3P 1 21/c 19.507; 9.4923; 14.387
90; 90.344; 90
1298.3Hassan, Haitham; Mohammed, Shireen; Robert, Frédéric; Landais, Yannick
Total Synthesis of (±)-Eucophylline. A Free-Radical Approach to the Synthesis of the Azabicyclo[3.3.1]nonane Skeleton.
Organic letters, 2015, 17, 4518-4521
1534103 CIFC24 H21 NP 1 21/c 17.4677; 18.793; 24.102
90; 94.988; 90
3369.7Hassan, Haitham; Mohammed, Shireen; Robert, Frédéric; Landais, Yannick
Total Synthesis of (±)-Eucophylline. A Free-Radical Approach to the Synthesis of the Azabicyclo[3.3.1]nonane Skeleton.
Organic letters, 2015, 17, 4518-4521
1534104 CIFC13 H14 B Cl F2 N2I 41/a :225.108; 25.108; 8.6289
90; 90; 90
5439.8Zhou, Xin; Yu, Changjiang; Feng, Zeya; Yu, Yang; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Highly Regioselective α-Chlorination of the BODIPY Chromophore with Copper(II) Chloride.
Organic letters, 2015, 17, 4632-4635
1534105 CIFC16 H11 B Cl2 F2 N2 OC 1 2/c 115.6318; 13.1816; 15.4701
90; 96.971; 90
3164.1Zhou, Xin; Yu, Changjiang; Feng, Zeya; Yu, Yang; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Highly Regioselective α-Chlorination of the BODIPY Chromophore with Copper(II) Chloride.
Organic letters, 2015, 17, 4632-4635
1534106 CIFC12 H11 B Cl2 F2 N2P -110.1284; 11.8356; 12.656
91.216; 110.273; 107.739
1341.8Zhou, Xin; Yu, Changjiang; Feng, Zeya; Yu, Yang; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Highly Regioselective α-Chlorination of the BODIPY Chromophore with Copper(II) Chloride.
Organic letters, 2015, 17, 4632-4635
1534107 CIFC20 H13 F3 O2 SP -17.4471; 9.4405; 12.781
79.059; 79.842; 75.136
844.95Xu, Chunfa; Shen, Qilong
Lewis Acid Mediated Trifluoromethylthio Lactonization/Lactamization.
Organic letters, 2015, 17, 4561-4563
1534108 CIFC24 H21 N O4 SP 1 21/n 18.2556; 14.406; 17.938
90; 93.63; 90
2129.1Liu, Hongxu; Yang, Yanyan; Wang, Shen; Wu, Jie; Wang, Xiao-Na; Chang, Junbiao
Synthesis of 3-Substituted 2-Aminochromones via Sn(IV)-Promoted Annulation of Ynamides with 2-Methoxyaroyl Chlorides.
Organic letters, 2015, 17, 4472-4475
1534109 CIFC14 H11 N O SP -15.9946; 7.961; 12.7201
85.167; 84.614; 73.532
578.51Lemercier, Bérénice C; Pierce, Joshua G.
Synthesis of 1,4,2-Oxathiazoles via Oxidative Cyclization of Thiohydroximic Acids.
Organic letters, 2015, 17, 4542-4545
1534110 CIFC25 H22 Cl2 I N3 O4 SP 1 21 110.469; 11.122; 11.473
90; 92.129; 90
1335Tripathi, Chandra Bhushan; Mukherjee, Santanu
Catalytic Enantioselective 1,4-Iodofunctionalizations of Conjugated Dienes.
Organic letters, 2015, 17, 4424-4427
1534111 CIFC18 H16 I N OP 1 21 19.9179; 5.7432; 14.186
90; 95.817; 90
803.88Tripathi, Chandra Bhushan; Mukherjee, Santanu
Catalytic Enantioselective 1,4-Iodofunctionalizations of Conjugated Dienes.
Organic letters, 2015, 17, 4424-4427
1534112 CIFC21 H21 N O5 SP 1 21 111.3632; 11.802; 15.831
90; 109.817; 90
1997.3Qiao, Baokun; Huang, Yin-Jun; Nie, Jing; Ma, Jun-An
Highly Regio-, Diastereo-, and Enantioselective Mannich Reaction of Allylic Ketones and Cyclic Ketimines: Access to Chiral Benzosultam.
Organic letters, 2015, 17, 4608-4611
1534113 CIFC19 H18 N2 O2P 1 21/c 111.7071; 15.8544; 9.4636
90; 113.637; 90
1609.2Shao, Jiaan; Liu, Xingyu; Shu, Ke; Tang, Pai; Luo, Jing; Chen, Wenteng; Yu, Yongping
Tuning the Annulation Reactivity of Vinyl Azides and Carbazates: A Divergent Synthesis of Aza-pyrimidinones and Imidazoles.
Organic letters, 2015, 17, 4502-4505
1534114 CIFC14 H17 N3 O4P 1 21/c 16.9191; 16.135; 14.3518
90; 104.515; 90
1551.09Shao, Jiaan; Liu, Xingyu; Shu, Ke; Tang, Pai; Luo, Jing; Chen, Wenteng; Yu, Yongping
Tuning the Annulation Reactivity of Vinyl Azides and Carbazates: A Divergent Synthesis of Aza-pyrimidinones and Imidazoles.
Organic letters, 2015, 17, 4502-4505
1534115 CIFC33 H25 N3 O2P 1 21/n 116.9438; 7.2054; 21.3218
90; 95.864; 90
2589.49Peng, Jing; Ran, Guang-Yao; Du, Wei; Chen, Ying-Chun
Divergent Cyclization Reactions of Morita-Baylis-Hillman Carbonates of 2-Cyclohexenone and Isatylidene Malononitriles.
Organic letters, 2015, 17, 4490-4493
1534116 CIFC27 H20 N4 O4P 1 21/c 17.3218; 32.2827; 11.6678
90; 91.975; 90
2756.25Peng, Jing; Ran, Guang-Yao; Du, Wei; Chen, Ying-Chun
Divergent Cyclization Reactions of Morita-Baylis-Hillman Carbonates of 2-Cyclohexenone and Isatylidene Malononitriles.
Organic letters, 2015, 17, 4490-4493
1534117 CIFC21 H19 F3 N4 O2P 1 21/c 122.1268; 5.3611; 16.7753
90; 101.52; 90
1949.86Chung, Tim S.; Lopez, Steven A.; Houk, K. N.; Garcia-Garibay, Miguel A
Stereospecific Synthesis of Substituted Aziridines by a Crystal-to-Crystal Photodenitrogenation of Δ(2)-1,2,3-Triazolines.
Organic letters, 2015, 17, 4568-4571
1534118 CIFC20 H18 F3 N3 O2P c a 2116.6564; 5.4719; 39.3699
90; 90; 90
3588.3Chung, Tim S.; Lopez, Steven A.; Houk, K. N.; Garcia-Garibay, Miguel A
Stereospecific Synthesis of Substituted Aziridines by a Crystal-to-Crystal Photodenitrogenation of Δ(2)-1,2,3-Triazolines.
Organic letters, 2015, 17, 4568-4571
1534119 CIFC53 H45 N2 O8P 21 21 2111.4428; 15.4354; 24.3994
90; 90; 90
4309.5Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.
Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.
Organic letters, 2015, 17, 4440-4443
1534120 CIFC48 H52 N4 O9P 21 21 214.958; 25.526; 11.093
90; 90; 90
4235.5Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.
Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.
Organic letters, 2015, 17, 4440-4443
1534121 CIFC45 H42 I2 N4 O8C 1 2/c 135.02; 16.0741; 20.002
90; 111.769; 90
10456Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.
Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.
Organic letters, 2015, 17, 4440-4443
1534122 CIFC59 H63 N6 O8C 1 2/c 120.0623; 15.4284; 19.2848
90; 120.843; 90
5125Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.
Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.
Organic letters, 2015, 17, 4440-4443
1534123 CIFC47 H48 N4 O8P 1 21/c 113.787; 14.6; 24.867
90; 105.219; 90
4829.9Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.
Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.
Organic letters, 2015, 17, 4440-4443
1534124 CIFC49 H50 Cl6 N4 O8P -113.203; 13.977; 14.658
90.494; 100.476; 113.249
2434.2Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.
Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.
Organic letters, 2015, 17, 4440-4443
1534125 CIFC45 H44 N4 O8P -112.2439; 13.8398; 14.5323
91.544; 97.532; 110.103
2285.7Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.
Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.
Organic letters, 2015, 17, 4440-4443
1534135 CIFC40 H59 Cl2 N2 P RuP 1 21/n 112.2117; 18.0562; 18.2926
90; 103.741; 90
3918Lummiss, Justin A. M.; Higman, Carolyn S.; Fyson, Devon L.; McDonald, Robert; Fogg, Deryn E.
The divergent effects of strong NHC donation in catalysis
Chem. Sci., 2015, 6, 6739
1534136 CIFC39 H35 N OP 1 21/c 119.39657; 15.07422; 10.4257
90; 98.9955; 90
3010.86Deng, Haiqin; He, Zikai; Lam, Jacky W. Y.; Tang, Ben Zhong
Regio- and stereoselective construction of stimuli-responsive macromolecules by a sequential coupling-hydroamination polymerization route
Polym. Chem., 2015, 6, 8297
1534348 CIFC20 H32 O3C 1 2 133.5582; 7.4109; 14.7554
90; 97.8284; 90
3635.4Du, Kun; De Mieri, Maria; Neuburger, Markus; Zietsman, Pieter C.; Marston, Andrew; van Vuuren, Sandy F.; Ferreira, Daneel; Hamburger, Matthias; van der Westhuizen, Jan H.
Labdane and Clerodane Diterpenoids from Colophospermum mopane.
Journal of natural products, 2015, 78, 2494-2504
1534351 CIFC16 H30 N2 O5 SP 6511.4458; 11.4458; 27.7551
90; 90; 120
3148.95Mazzier, Daniela; Carraro, Francesco; Crisma, Marco; Rancan, Marzio; Toniolo, Claudio; Moretto, Alessandro
A terminally protected dipeptide: from crystal structure and self-assembly, through co-assembly with carbon-based materials, to a ternary catalyst for reduction chemistry in water.
Soft matter, 2015, 12, 238-245
1534352 CIFC16 H30 N2 O5 SP 21 21 215.08911; 12.09583; 32.4406
90; 90; 90
1996.95Mazzier, Daniela; Carraro, Francesco; Crisma, Marco; Rancan, Marzio; Toniolo, Claudio; Moretto, Alessandro
A terminally protected dipeptide: from crystal structure and self-assembly, through co-assembly with carbon-based materials, to a ternary catalyst for reduction chemistry in water.
Soft matter, 2015, 12, 238-245
1534401 CIFC38 H57 Cl F19 N7 O5 P3 RuP -110.036; 14.855; 18.895
73.62; 76.36; 87.09
2626Du, Jun; Zhang, Erlong; Zhao, Yao; Zheng, Wei; Zhang, Yang; Lin, Yu; Wang, Zhaoying; Luo, Qun; Wu, Kui; Wang, Fuyi
Discovery of a dual-targeting organometallic ruthenium complex with high activity inducing early stage apoptosis of cancer cells.
Metallomics : integrated biometal science, 2015, 7, 1573-1583
1538419 CIFC24.5 H27 Br2 Cl O6P 21 21 219.7566; 19.1985; 27.6028
90; 90; 90
5170.34Hans, Marcus; Charpentier, Maël; Huch, Volker; Jauch, Johann; Bruhn, Torsten; Bringmann, Gerhard; Quandt, Dietmar
Stereoisomeric Composition of Natural Myrtucommulone A.
Journal of natural products, 2015, 78, 2381-2389
1538420 CIFC48 H55 F3 O10P 1 21 16.4479; 40.961; 17.888
90; 91.687; 90
4722.4Hans, Marcus; Charpentier, Maël; Huch, Volker; Jauch, Johann; Bruhn, Torsten; Bringmann, Gerhard; Quandt, Dietmar
Stereoisomeric Composition of Natural Myrtucommulone A.
Journal of natural products, 2015, 78, 2381-2389
1539135 CIFC20 H15 Cl N2 O3P 1 21/n 116.571; 5.5448; 20.45
90; 111.604; 90
1747Li, Danyang; Yu, Ming; Zhang, Jitan; Liu, Zhanxiang; Zhang, Yuhong
Synthesis of Benzyl Esters via Functionalization of Multiple C-H Bonds by Palladium Catalysis.
Organic letters, 2015, 17, 5300-5303
1540018 CIFC24 H20 Dy2 N2 O17C 1 2/c 118.3085; 9.0788; 19.6464
90; 97.068; 90
3240.8Liu, Ke; Li, Huanhuan; Zhang, Xuejing; Shi, Wei; Cheng, Peng
Constraining and Tuning the Coordination Geometry of a Lanthanide Ion in Metal-Organic Frameworks: Approach toward a Single-Molecule Magnet.
Inorganic chemistry, 2015, 54, 10224-10231
1540019 CIFC26 H28 Dy2 N2 O19C 1 2/c 118.465; 9.2442; 19.699
90; 102.18; 90
3286.8Liu, Ke; Li, Huanhuan; Zhang, Xuejing; Shi, Wei; Cheng, Peng
Constraining and Tuning the Coordination Geometry of a Lanthanide Ion in Metal-Organic Frameworks: Approach toward a Single-Molecule Magnet.
Inorganic chemistry, 2015, 54, 10224-10231
1540020 CIFC24 H20 Dy2 N2 O17P n m a8.6326; 28.1206; 15.3462
90; 90; 90
3725.3Liu, Ke; Li, Huanhuan; Zhang, Xuejing; Shi, Wei; Cheng, Peng
Constraining and Tuning the Coordination Geometry of a Lanthanide Ion in Metal-Organic Frameworks: Approach toward a Single-Molecule Magnet.
Inorganic chemistry, 2015, 54, 10224-10231
1540021 CIFC10 H12 B F4 N O2 RuP 1 21/n 18.7303; 9.7841; 15.4342
90; 91.525; 90
1317.89Nyawade, Eunice A.; Friedrich, Holger B.; Omondi, Bernard; Mpungose, Philani
Synthesis and Characterization of New (η5-Cyclopentadienyl)dicarbonylruthenium(II) Amine Complexes: Their Application as Homogeneous Catalysts in Styrene Oxidation
Organometallics, 2015, 34, 4922
1540022 CIFC14 H14 B F4 N O2 RuP 1 21/n 110.4488; 9.7788; 31.7901
90; 99.236; 90
3206.1Nyawade, Eunice A.; Friedrich, Holger B.; Omondi, Bernard; Mpungose, Philani
Synthesis and Characterization of New (η5-Cyclopentadienyl)dicarbonylruthenium(II) Amine Complexes: Their Application as Homogeneous Catalysts in Styrene Oxidation
Organometallics, 2015, 34, 4922
1540024 CIFC42 H49 Cl2 Eu N12 O16 ZnP -113.8641; 14.5627; 15.19
96.519; 113.081; 109.85
2543.6Anastasiadis, Nikolaos C.; Polyzou, Christina D.; Kostakis, George E.; Bekiari, Vlasoula; Lan, Yanhua; Perlepes, Spyros P.; Konidaris, Konstantis F.; Powell, Annie K.
Dinuclear lanthanide(iii)/zinc(ii) complexes with methyl 2-pyridyl ketone oxime.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 19791-19795
1540025 CIFC28 H29 Dy N10 O10 ZnC 1 c 115.9387; 9.3158; 22.5168
90; 94.59; 90
3332.6Anastasiadis, Nikolaos C.; Polyzou, Christina D.; Kostakis, George E.; Bekiari, Vlasoula; Lan, Yanhua; Perlepes, Spyros P.; Konidaris, Konstantis F.; Powell, Annie K.
Dinuclear lanthanide(iii)/zinc(ii) complexes with methyl 2-pyridyl ketone oxime.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 19791-19795
1540029 CIFC28 H20 Cu O7P 1 21/n 112.3691; 13.9416; 13.8663
90; 100.45; 90
2351.5Jochyms, Quentin; Guillot, Pierre; Mignard, Emmanuel; Vincent, Jean-Marc
A fluorosurfactant and photoreducible Cu(II)-tren click catalyst: surfactant and catalytic properties at liquid/liquid interfaces.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 19700-19707
1540030 CIFC46 H58 Dy2 N14 O24P -19.931; 10.841; 14.4817
82.775; 71.167; 74.627
1421.48Kuo, Che-Jung; Holmberg, Rebecca J.; Lin, Po-Heng
Slight synthetic changes eliciting different topologies: synthesis, structure and magnetic properties of novel dinuclear and nonanuclear dysprosium complexes.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 19758-19762
1540031 CIFC80 H92 Dy9 N24 O46C 1 2/c 134.8579; 24.5497; 24.2872
90; 120.453; 90
17916.6Kuo, Che-Jung; Holmberg, Rebecca J.; Lin, Po-Heng
Slight synthetic changes eliciting different topologies: synthesis, structure and magnetic properties of novel dinuclear and nonanuclear dysprosium complexes.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 19758-19762
1540032 CIFC28.5 H63 Cl2 Cu2 N4 O19 Zn2P -110.9593; 13.8454; 17.4039
109.186; 90.177; 108.009
2355.8Heras Ojea, María José; Wilson, Claire; Coles, Simon J.; Tuna, Floriana; Murrie, Mark
Directed synthesis of {CuZn} and {CuZn} heterometallic complexes.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 19275-19281
1540033 CIFC88 H232 Cl8 Cu8 N16 O96 Zn8P 4/n26.5574; 26.5574; 13.1186
90; 90; 90
9252.5Heras Ojea, María José; Wilson, Claire; Coles, Simon J.; Tuna, Floriana; Murrie, Mark
Directed synthesis of {CuZn} and {CuZn} heterometallic complexes.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 19275-19281
1540373 CIFC135 H42 Cl3 O2C 1 2/c 120.4242; 25.5132; 32.3262
90; 105.672; 90
16218.5Abeyratne Kuragama, Peumie L.; Fronczek, Frank R.; Sygula, Andrzej
Bis-corannulene Receptors for Fullerenes Based on Klärner's Tethers: Reaching the Affinity Limits.
Organic letters, 2015, 17, 5292-5295
1540374 CIFC16 H26 N2 O6 SP 21 21 216.2372; 11.1508; 28.596
90; 90; 90
1988.8Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François
Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.
Organic letters, 2015, 17, 5408-5411
1540375 CIFC13 H21 N O6P 21 21 216.282; 9.924; 24.859
90; 90; 90
1549.8Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François
Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.
Organic letters, 2015, 17, 5408-5411
1540376 CIFC16 H27 N O8P 1 21 110.248; 9.553; 11.932
90; 99.477; 90
1152.2Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François
Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.
Organic letters, 2015, 17, 5408-5411
1540377 CIFC17 H28 N2 O6P 1 21 110.375; 17.5559; 10.8576
90; 95.023; 90
1970Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François
Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.
Organic letters, 2015, 17, 5408-5411
1540378 CIFC19 H24 N2 O6 SP 1 21 111.0948; 6.112; 15.1863
90; 92.704; 90
1028.7Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François
Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.
Organic letters, 2015, 17, 5408-5411
1540379 CIFC20 H26 N2 O6P 1 21 19.6081; 10.7346; 20.0544
90; 91.493; 90
2067.7Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François
Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.
Organic letters, 2015, 17, 5408-5411
1540380 CIFC84 H153 Ag3 Au15 O2 S14C 1 2/c 124.9951; 18.5586; 51.826
90; 90.478; 90
24040Xiang, Ji; Li, Peng; Song, Yongbo; Liu, Xia; Chong, Hanbao; Jin, Shan; Pei, Yong; Yuan, Xiaoyou; Zhu, Manzhou
X-Ray crystal structure, and optical and electrochemical properties of the Au15Ag3(SC6H11)14 nanocluster with a core-shell structure.
Nanoscale, 2015, 7, 18278-18283
1540381 CIFC21 H24 Cl Co N7 NiP 1 21/n 114.4536; 9.9877; 14.7366
90; 101.065; 90
2087.8Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C.
Configuring Bonds between First-Row Transition Metals.
Accounts of chemical research, 2015, 48, 2885-2894
1540382 CIFC41 H64 Fe N4 O0.5 P3 TiP -112.35; 19.4587; 19.7453
113.034; 95.547; 101.183
4204.9Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C.
Configuring Bonds between First-Row Transition Metals.
Accounts of chemical research, 2015, 48, 2885-2894
1540383 CIFC43 H68 N4 Ni O P3 TiP -112.5471; 14.0969; 24.6228
91.787; 98.742; 94.687
4286Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C.
Configuring Bonds between First-Row Transition Metals.
Accounts of chemical research, 2015, 48, 2885-2894
1540384 CIFC69 H91 B Co Cr N5 O P3P 1 21/c 117.8979; 14.3708; 26.8674
90; 99.446; 90
6816.8Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C.
Configuring Bonds between First-Row Transition Metals.
Accounts of chemical research, 2015, 48, 2885-2894
1540385 CIFC39 H60 B Cr F4 N4 Ni P3R -3 :H12.4121; 12.4121; 57.067
90; 90; 120
7613.9Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C.
Configuring Bonds between First-Row Transition Metals.
Accounts of chemical research, 2015, 48, 2885-2894
1540386 CIFC21 H24 Cl Co N7 NiP 1 21/n 114.4978; 10.0084; 14.7758
90; 100.944; 90
2105Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C.
Configuring Bonds between First-Row Transition Metals.
Accounts of chemical research, 2015, 48, 2885-2894
1540387 CIFC78 H196 Cu6 Li4 Mn4 N12 O104P 4/m m m36.71; 36.71; 15.414
90; 90; 90
20772Grancha, Thais; Acosta, Alvaro; Cano, Joan; Ferrando-Soria, Jesús; Seoane, Beatriz; Gascon, Jorge; Pasán, Jorge; Armentano, Donatella; Pardo, Emilio
Cation Exchange in Dynamic 3D Porous Magnets: Improvement of the Physical Properties.
Inorganic chemistry, 2015, 54, 10834-10840
1540388 CIFC78 H198 Cu6 K4 Mn4 N12 O105P 4/m m m37.492; 37.492; 15.557
90; 90; 90
21868Grancha, Thais; Acosta, Alvaro; Cano, Joan; Ferrando-Soria, Jesús; Seoane, Beatriz; Gascon, Jorge; Pasán, Jorge; Armentano, Donatella; Pardo, Emilio
Cation Exchange in Dynamic 3D Porous Magnets: Improvement of the Physical Properties.
Inorganic chemistry, 2015, 54, 10834-10840
1540389 CIFC19 H24 F2 N3 Na O7 SP 1 21/c 115.929; 10.828; 13.718
90; 91.62; 90
2365.1Jiang, Chen; Wang, Yongli; Yan, Jiaqi; Yang, Jingxiang; Xiao, Liping; Hao, Hongxun
Formation Mechanism and Phase Transformation Behaviors of Pantoprazole Sodium Heterosolvate
Organic Process Research & Development, 2015, 19, 1752
1540392 CIFBa0.1 O4 Si Sr1.9P m n b5.674; 7.086; 9.745
90; 90; 90
391.81Li, Xiaojun; Hua, Youjie; Ma, Hongping; Deng, Degang; Xu, Shiqing
Modification of the crystal structure of Sr2−xBaxSi(O,N)4: Eu2+phosphors to improve their luminescence properties
CrystEngComm, 2015, 17, 9123
1540393 CIFBa0.15 N O4 Si Sr2.85P m n b5.6796; 7.1386; 9.7639
90; 90; 90
395.87Li, Xiaojun; Hua, Youjie; Ma, Hongping; Deng, Degang; Xu, Shiqing
Modification of the crystal structure of Sr2−xBaxSi(O,N)4: Eu2+phosphors to improve their luminescence properties
CrystEngComm, 2015, 17, 9123
1540394 CIFC17 H16 B Mo N6 O2 P3P -18.7379; 9.957; 13.2391
104.609; 96.252; 107.11
1044.19Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540395 CIFC38 H38 B2 Fe N12 P6P -110.981; 13.5289; 15.9001
91.94; 99.962; 111.752
2148.4Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540396 CIFC34.5 H34 B2 Cd N12 P6P -114.048; 14.097; 14.1551
66.977; 61.712; 61.256
2115.4Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540397 CIFC38 H38 B2 Co N12 P6P -111.132; 13.749; 15.6951
90.726; 99.272; 112.266
2186.9Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540398 CIFC38 H38 B2 N12 Ni P6P -111.091; 13.6971; 15.735
90.977; 99.368; 112.091
2177.3Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540399 CIFC32 H30 B3 Cl6 Co F4 N12 P6C 1 2/c 111.2374; 17.1902; 24.3814
90; 97.463; 90
4669.9Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540400 CIFC12 H11 B N6 P3 TlP n m a9.144; 10.3091; 17.5949
90; 90; 90
1658.61Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540401 CIFC12 H11 B Cl3 N6 P3 TiP 1 21/m 18.281; 10.292; 11.4621
90; 102.607; 90
953.34Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540402 CIFC15 H11 B Mn N6 O3 P3P 1 21/c 116.962; 10.482; 24.6311
90; 112.579; 90
4043.6Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540403 CIFC21 H23 B N7 P3 PdP 1 21/c 19.404; 15.931; 16.528
90; 100.27; 90
2436.5Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540404 CIFC22 H16 Cu N14 OP -112.3344; 14.2954; 15.4511
95.631; 107.583; 108.242
2410.1Saha, Manideepa; Das, Mriganka; Nasani, Rajendar; Choudhuri, Indrani; Yousufuddin, Muhammed; Nayek, Hari Pada; Shaikh, Mobin M.; Pathak, Biswarup; Mukhopadhyay, Suman
Targeted water soluble copper-tetrazolate complexes: interactions with biomolecules and catecholase like activities.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20154-20167
1540405 CIFC29 H23 Cu N12 O3.5P -111.9248; 11.9276; 13.4576
71.6; 68.381; 70.668
1637.7Saha, Manideepa; Das, Mriganka; Nasani, Rajendar; Choudhuri, Indrani; Yousufuddin, Muhammed; Nayek, Hari Pada; Shaikh, Mobin M.; Pathak, Biswarup; Mukhopadhyay, Suman
Targeted water soluble copper-tetrazolate complexes: interactions with biomolecules and catecholase like activities.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20154-20167
1540406 CIFC24.65 H18 Cr Gd N8 Ni O10.65P 1 21/c 113.071; 12.139; 21.735
90; 106.84; 90
3300.8Chen, Chao; Liu, Yashu; Li, Ping; Zhou, Hongbo; Shen, Xiaoping
Construction of Ni(II)Ln(III)M(III) (Ln = Gd(III), Tb(III); M = Fe(III), Cr(III)) clusters showing slow magnetic relaxations.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20193-20199
1540407 CIFC24.63 H20.52 Cr N8 Ni O10.63 TbP 1 21/c 113.051; 12.15; 21.711
90; 106.89; 90
3294.2Chen, Chao; Liu, Yashu; Li, Ping; Zhou, Hongbo; Shen, Xiaoping
Construction of Ni(II)Ln(III)M(III) (Ln = Gd(III), Tb(III); M = Fe(III), Cr(III)) clusters showing slow magnetic relaxations.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20193-20199
1540408 CIFC25 H18 Fe N8 Ni O11 TbP 1 21/c 112.861; 12.014; 21.577
90; 106.73; 90
3192.8Chen, Chao; Liu, Yashu; Li, Ping; Zhou, Hongbo; Shen, Xiaoping
Construction of Ni(II)Ln(III)M(III) (Ln = Gd(III), Tb(III); M = Fe(III), Cr(III)) clusters showing slow magnetic relaxations.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20193-20199
1540409 CIFC24 H18 Fe Gd N8 Ni O11P 1 21/c 112.862; 12.012; 21.58
90; 106.72; 90
3193.1Chen, Chao; Liu, Yashu; Li, Ping; Zhou, Hongbo; Shen, Xiaoping
Construction of Ni(II)Ln(III)M(III) (Ln = Gd(III), Tb(III); M = Fe(III), Cr(III)) clusters showing slow magnetic relaxations.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20193-20199
1540410 CIFC142 H120 Gd7 N11 O24P -115.5132; 20.762; 24.831
106.288; 103.085; 105.827
6977.1Mazarakioti, Eleni C.; Cunha-Silva, Luís; Bekiari, Vlasoula; Escuer, Albert; Stamatatos, Theocharis C.
New structural topologies in 4f-metal cluster chemistry from vertex-sharing butterfly units: {LnIII7} complexes exhibiting slow magnetization relaxation and ligand-centred emissions
RSC Advances, 2015, 5, 92534-92538
1540411 CIFC23 H20 N2 OP -19.7936; 10.0349; 10.3079
110.403; 101.163; 102.888
883.8Dandia, Anshu; Sharma, Amit; Parewa, Vijay; Kumawat, Begraj; Rathore, Kuldeep S.; Sharma, Amit
Amidic C–N bond cleavage of isatin: chemoselective synthesis of pyrrolo[2,3,4- <i>kl</i> ]acridin-1-ones using Ag NPs decorated rGO composite as an efficient and recoverable catalyst under microwave irradiation
RSC Advances, 2015, 5, 91888-91902
1540412 CIFC29 H24 N2 O2 SeP 21 21 218.7794; 14.6701; 37.5122
90; 90; 90
4831.4Chang, Wong-Jin; Kulkarni, Manohar V.; Sun, Chung-Ming
Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication
RSC Advances, 2015, 5, 97113-97120
1540413 CIFC31 H28 N2 O3 SeP 1 21 18.6504; 9.7776; 16.3783
90; 98.688; 90
1369.38Chang, Wong-Jin; Kulkarni, Manohar V.; Sun, Chung-Ming
Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication
RSC Advances, 2015, 5, 97113-97120
1540414 CIFC22 H23 Br N2 O2 S SeP 1 21 111.244; 7.6728; 12.837
90; 98.983; 90
1093.9Chang, Wong-Jin; Kulkarni, Manohar V.; Sun, Chung-Ming
Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication
RSC Advances, 2015, 5, 97113-97120
1540415 CIFC16 H15 N SeP 1 21/n 114.8679; 10.004; 18.5854
90; 98.871; 90
2731.3Chang, Wong-Jin; Kulkarni, Manohar V.; Sun, Chung-Ming
Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication
RSC Advances, 2015, 5, 97113-97120
1540425 CIFC18 H14 N O4C 2 2 216.8797; 17.32; 26.023
90; 90; 90
3100.8Artuso, Emma; Ghibaudi, Elena; Lace, Beatrice; Marabello, Domenica; Vinciguerra, Daniele; Lombardi, Chiara; Koltai, Hinanit; Kapulnik, Yoram; Novero, Mara; Occhiato, Ernesto G.; Scarpi, Dina; Parisotto, Stefano; Deagostino, Annamaria; Venturello, Paolo; Mayzlish-Gati, Einav; Bier, Ariel; Prandi, Cristina
Stereochemical Assignment of Strigolactone Analogues Confirms Their Selective Biological Activity.
Journal of natural products, 2015, 78, 2624-2633
1540426 CIFC32 H32 O15P 21 21 217.0833; 13.9608; 31.0735
90; 90; 90
3072.81Wu, Guangwei; Yu, Guihong; Kurtán, Tibor; Mándi, Attila; Peng, Jixing; Mo, Xiaomei; Liu, Ming; Li, Hui; Sun, Xinhua; Li, Jing; Zhu, Tianjiao; Gu, Qianqun; Li, Dehai
Versixanthones A-F, Cytotoxic Xanthone-Chromanone Dimers from the Marine-Derived Fungus Aspergillus versicolor HDN1009.
Journal of natural products, 2015, 78, 2691-2698
1540465 CIFC28 H40 O8P 43 21 210.5228; 10.5228; 52.456
90; 90; 90
5808.4Nguyen, Ha T. T.; Truong, Ngan B.; Doan, Huong T. M.; Litaudon, Marc; Retailleau, Pascal; Do, Thao T.; Nguyen, Hung V.; Chau, Minh V.; Pham, Cuong V.
Cytotoxic Clerodane Diterpenoids from the Leaves of Casearia grewiifolia.
Journal of natural products, 2015, 78, 2726-2730
1540466 CIFC38.5 H52 O10.5P 3118.4501; 18.4501; 9.9236
90; 90; 120
2925.5Nguyen, Ha T. T.; Truong, Ngan B.; Doan, Huong T. M.; Litaudon, Marc; Retailleau, Pascal; Do, Thao T.; Nguyen, Hung V.; Chau, Minh V.; Pham, Cuong V.
Cytotoxic Clerodane Diterpenoids from the Leaves of Casearia grewiifolia.
Journal of natural products, 2015, 78, 2726-2730
1540468 CIFC20 H16 Br N OP 21 21 215.616; 13.1439; 22.937
90; 90; 90
1693.1Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran
Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect
Chem. Sci., 2015
1540469 CIFC16 H15 Br NP b c a16.0499; 7.6796; 22.6554
90; 90; 90
2792.4Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran
Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect
Chem. Sci., 2015
1540470 CIFC22 H20 Br N OP 1 21/n 19.5118; 19.672; 9.821
90; 91.45; 90
1837.1Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran
Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect
Chem. Sci., 2015
1540471 CIFC17 H18 Br NP b c a17.503; 8.0333; 21.133
90; 90; 90
2971.4Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran
Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect
Chem. Sci., 2015
1540472 CIFC23 H22 Br N OC 1 2/c 118.368; 9.0221; 23.995
90; 102.82; 90
3877.3Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran
Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect
Chem. Sci., 2015
1540473 CIFC18 H20 Br NP b c a16.319; 8.0724; 24.455
90; 90; 90
3221.5Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran
Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect
Chem. Sci., 2015
1540474 CIFC24 H24 Br N OP 1 21/n 15.7109; 12.738; 28.186
90; 90.021; 90
2050.4Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran
Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect
Chem. Sci., 2015
1540475 CIFC18 H19 N O3P 21 21 216.1323; 7.4365; 33.4178
90; 90; 90
1523.95Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540476 CIFC19 H21 N O3P 1 21 18.719; 5.6224; 17.2361
90; 96.032; 90
840.26Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540477 CIFC18 H21 N O4C 1 2 114.0792; 6.7979; 17.748
90; 95.958; 90
1689.47Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540478 CIFC19 H21 N O3P 21 21 217.3552; 13.6032; 17.2196
90; 90; 90
1722.89Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540479 CIFC18 H19 N O3P 21 21 215.9065; 7.9113; 32.9027
90; 90; 90
1537.48Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540480 CIFC18 H17 N O2P 21 21 216.0722; 8.115; 29.7039
90; 90; 90
1463.69Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540481 CIFC21 H19 N O4P b c a9.4116; 15.8331; 24.7415
90; 90; 90
3686.8Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540482 CIFC19 H21 N O3P 1 21 18.5617; 5.5085; 17.2021
90; 103.015; 90
790.45Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530

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