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

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