Crystallography Open Database

Result: there are 527382 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format

We are unable to provide that many records as a single archive.
You can instead download the entire COD archive as a single .zip, .tgz or .txz archive.

Displaying all data in COD

Blue left arrow Blue left arrow First | Blue left arrow Previous 300 | of 1758 | Next 300 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
1518416 CIFC34 H35 N O14P 17.4957; 12.0298; 17.8347
87.387; 87.555; 74.708		1548.85Moon, Kyuho; Chung, Beomkoo; Shin, Yoonho; Rheingold, Arnold L.; Moore, Curtis E.; Park, Sung Jean; Park, Sunghyouk; Lee, Sang Kook; Oh, Ki-Bong; Shin, Jongheon; Oh, Dong-Chan
Pentacyclic antibiotics from a tidal mud flat-derived actinomycete.
Journal of natural products, 2015, 78, 524-529
1518417 CIFC17 H23 Br O5C 1 2 118.8295; 7.8451; 11.4443
90; 95.208; 90		1683.57Shockley, Samantha E.; Holder, Jeffrey C.; Stoltz, Brian M.
A catalytic, enantioselective formal synthesis of (+)-dichroanone and (+)-taiwaniaquinone H.
Organic letters, 2014, 16, 6362-6365
1518418 CIFC48 H44 B2 F8 Fe N4 P2P 1 21 19.834; 19.1669; 12.3417
90; 106.885; 90		2226Bigler, Raphael; Mezzetti, Antonio
Isonitrile iron(II) complexes with chiral N2P2 macrocycles in the enantioselective transfer hydrogenation of ketones.
Organic letters, 2014, 16, 6460-6463
1518419 CIFC25 H22 N2 OI 1 2/c 117.688; 10.0067; 21.9732
90; 100.303; 90		3826.5Yang, Xiu-Long; Chen, Fei; Zhou, Neng-Neng; Yu, Wei; Han, Bing
Synthesis of isoxazoline-functionalized phenanthridines via iminoxyl radical-participated cascade sequence.
Organic letters, 2014, 16, 6476-6479
1518420 CIFC15 H15 N OP 419.0756; 9.0756; 15.824
90; 90; 90		1303.4Ran, Rui-Qiao; Xiu, Shi-Dong; Li, Chuan-Ying
Synthesis of N-acylamidines via rhodium-catalyzed reaction of nitrosobenzene derivatives with N-sulfonyl-1,2,3-triazoles.
Organic letters, 2014, 16, 6394-6396
1518421 CIFC23 H28 N2 O4 SP 1 21/n 110.543; 9.344; 22.465
90; 92.128; 90		2211.6Xu, Hua-Dong; Jia, Zhi-Hong; Xu, Ke; Zhou, Hao; Shen, Mei-Hua
One-Pot Protocol to Functionalized Benzopyrrolizidine Catalyzed Successively by Rh2(OAc)4 and Cu(OTf)2: A Transition Metal-Lewis Acid Catalysis Relay.
Organic letters, 2015, 17, 66-69
1518422 CIFC23 H28 N2 O4 SP n a 2126.688; 18.145; 9.062
90; 90; 90		4388.3Xu, Hua-Dong; Jia, Zhi-Hong; Xu, Ke; Zhou, Hao; Shen, Mei-Hua
One-Pot Protocol to Functionalized Benzopyrrolizidine Catalyzed Successively by Rh2(OAc)4 and Cu(OTf)2: A Transition Metal-Lewis Acid Catalysis Relay.
Organic letters, 2015, 17, 66-69
1518423 CIFC59 H17 F25 N6P -114.3298; 15.1659; 17.3878
100.804; 113.243; 106.844		3121.3Zhang, Kai; Wei, Pingchun; Li, Xin; Ågren, Hans; Xie, Yongshu
Oxidative ring closure and metal triggered ring opening: syntheses of macrocyclic and linear hexapyrroles.
Organic letters, 2014, 16, 6354-6357
1518424 CIFC61 H19 Cu F25 N6 O2P -115.04; 15.1401; 16.0989
98.35; 97.875; 118.146		3108.1Zhang, Kai; Wei, Pingchun; Li, Xin; Ågren, Hans; Xie, Yongshu
Oxidative ring closure and metal triggered ring opening: syntheses of macrocyclic and linear hexapyrroles.
Organic letters, 2014, 16, 6354-6357
1518425 CIFC59 H12 F25 Fe N6 O2P 21 21 2112.2942; 15.4624; 27.665
90; 90; 90		5259.1Zhang, Kai; Wei, Pingchun; Li, Xin; Ågren, Hans; Xie, Yongshu
Oxidative ring closure and metal triggered ring opening: syntheses of macrocyclic and linear hexapyrroles.
Organic letters, 2014, 16, 6354-6357
1518426 CIFC19 H16 O5P 21 21 28.5692; 21.534; 7.9705
90; 90; 90		1470.79Centko, Ryan M.; Steinø, Anne; Rosell, Federico I.; Patrick, Brian O.; de Voogd, Nicole; Mauk, A. Grant; Andersen, Raymond J.
Indoleamine 2,3-dioxygenase inhibitors isolated from the sponge Xestospongia vansoesti: structure elucidation, analogue synthesis, and biological activity.
Organic letters, 2014, 16, 6480-6483
1518427 CIFC15 H9 F3 N2 O2P 1 21/n 116.6085; 7.853; 20.7239
90; 103.721; 90		2625.8Kumar, Shailesh; Rathore, Vandana; Verma, Ajay; Prasad, Ch Durga; Kumar, Amit; Yadav, Abhimanyu; Jana, Sadhan; Sattar, Moh; Meenakshi, ?; Kumar, Sangit
KO(t)Bu-Mediated Aerobic Transition-Metal-Free Regioselective β-Arylation of Indoles: Synthesis of β-(2-/4-Nitroaryl)-indoles.
Organic letters, 2015, 17, 82-85
1518428 CIFC15 H11 Cl N2 O2C 1 2/c 119.16; 11.3942; 15.345
90; 126.612; 90		2689Kumar, Shailesh; Rathore, Vandana; Verma, Ajay; Prasad, Ch Durga; Kumar, Amit; Yadav, Abhimanyu; Jana, Sadhan; Sattar, Moh; Meenakshi, ?; Kumar, Sangit
KO(t)Bu-Mediated Aerobic Transition-Metal-Free Regioselective β-Arylation of Indoles: Synthesis of β-(2-/4-Nitroaryl)-indoles.
Organic letters, 2015, 17, 82-85
1518429 CIFC29 H25 N O2 S2P -111.2483; 12.9991; 18.089
99.988; 99.239; 102.072		2493.5Han, Dandan; Li, Zhiming; Fan, Renhua
Oxidative nucleophilic cyclization of 2-alkynylanilines with thiophenols under metal-free conditions.
Organic letters, 2014, 16, 6508-6511
1518430 CIFC27 H24 O3P b c a16.33; 15.14; 17.416
90; 90; 90		4306Seetha Lakshmi, K. C.; Krishnan, Jagadeesh; Sinu, C. R.; Varughese, Sunil; Nair, Vijay
N-heterocyclic carbene catalyzed annulation of enals to aurone analogs: synthesis of cyclopentene-fused spirobenzofuran-3-ones.
Organic letters, 2014, 16, 6374-6377
1518431 CIFC21 H22 F N O4P 1 21/c 15.848; 12.3; 25.729
90; 91.785; 90		1849.8Reddy, B. V. Subba; Swathi, V.; Swain, Manisha; Bhadra, Manika Pal; Sridhar, B.; Satyanarayana, D.; Jagadeesh, B.
Stereoselective synthesis of spiro[tetrahydropyran-3,3'-oxindole] derivatives employing Prins cascade strategy.
Organic letters, 2014, 16, 6267-6269
1518432 CIFC6 H12 O6P 21 21 2110.336; 14.852; 4.924
90; 90; 90		755.9Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518433 CIFC6 H12 O6P 21 21 2110.26; 14.837; 4.8169
90; 90; 90		733.3Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518434 CIFC6 H12 O6P 21 21 2110.22; 14.832; 4.7689
90; 90; 90		722.9Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518435 CIFC6 H12 O6P 21 21 2110.218; 14.823; 4.7439
90; 90; 90		718.5Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518436 CIFC6 H12 O6P 21 21 2110.181; 14.808; 4.693
90; 90; 90		707.5Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518437 CIFC6 H12 O6P 21 21 2110.11; 14.808; 4.5801
90; 90; 90		685.7Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518438 CIFC6 H12 O6P 21 21 2110.06; 14.798; 4.537
90; 90; 90		675.4Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518439 CIFC6 H12 O6P 21 21 2110.05; 14.807; 4.4206
90; 90; 90		657.8Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518440 CIFC6 H12 O6P 21 21 2110.04; 14.796; 4.3879
90; 90; 90		651.8Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518441 CIFC6 H12 O6P 21 21 2110.056; 14.779; 4.275
90; 90; 90		635.3Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518442 CIFC6 H12 O6P 21 21 2110.059; 14.776; 4.261
90; 90; 90		633.3Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518443 CIFC6 H12 O6P 21 21 2110.063; 14.787; 4.256
90; 90; 90		633.3Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518444 CIFC6 H12 O6P 21 21 219.714; 14.99; 4.262
90; 90; 90		621Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518445 CIFC6 H12 O6P 21 21 219.73; 14.987; 4.234
90; 90; 90		617.4Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518446 CIFC6 H12 O6P 21 21 219.694; 14.931; 4.2234
90; 90; 90		611.3Patyk, Ewa; Katrusiak, Andrzej
Transformable H-bonds and conformation in compressed glucose
Chem. Sci., 2015, 6, 1991
1518447 CIFC67 F6P b c a9.9998; 20.6538; 31.3512
90; 90; 90		6475.1San, Long K.; Bukovsky, Eric V.; Larson, Bryon W.; Whitaker, James B.; Deng, S. H. M.; Kopidakis, Nikos; Rumbles, Garry; Popov, Alexey A.; Chen, Yu-Sheng; Wang, Xue-Bin; Boltalina, Olga V.; Strauss, Steven H.
A faux hawk fullerene with PCBM-like properties
Chem. Sci., 2015, 6, 1801
1518448 CIFC60 H60 Li4 O5 Rb4C m c m14.166; 13.519; 25.901
90; 90; 90		4960Filatov, Alexander S.; Spisak, Sarah N.; Zabula, Alexander V.; McNeely, James; Rogachev, Andrey Yu.; Petrukhina, Marina A.
Self-assembly of tetrareduced corannulene with mixed Li‒Rb clusters: dynamic transformations, unique structures and record7Li NMR shifts
Chem. Sci., 2015, 6, 1959
1518449 CIFC66 H80 Li3 O12.5 Rb5P -110.064; 15.27; 22.129
90.416; 93.102; 94.532		3384.9Filatov, Alexander S.; Spisak, Sarah N.; Zabula, Alexander V.; McNeely, James; Rogachev, Andrey Yu.; Petrukhina, Marina A.
Self-assembly of tetrareduced corannulene with mixed Li–Rb clusters: dynamic transformations, unique structures and record7Li NMR shifts
Chem. Sci., 2015, 6, 1959
1518450 CIFC28 H46 N4 O19 TmC 1 c 123.1686; 9.677; 16.8001
90; 118.272; 90		3317.3Funk, Alexander M.; Finney, Katie-Louise N. A.; Harvey, Peter; Kenwright, Alan M.; Neil, Emily R.; Rogers, Nicola J.; Kanthi Senanayake, P.; Parker, David
Critical analysis of the limitations of Bleaney's theory of magnetic anisotropy in paramagnetic lanthanide coordination complexes
Chem. Sci., 2015, 6, 1655
1518451 CIFC33 H31.75 N2 O5.88C 1 2 152.27; 5.01; 22.83
90; 105.49; 90		5761Raeburn, Jaclyn; Mendoza-Cuenca, Cristina; Cattoz, Beatrice N.; Little, Marc A.; Terry, Ann E.; Zamith Cardoso, Andre; Griffiths, Peter C.; Adams, Dave J.
The effect of solvent choice on the gelation and final hydrogel properties of Fmoc-diphenylalanine.
Soft matter, 2015, 11, 927-935
1518452 CIFC36 H58 Cl N3 O2P 3215.865; 15.865; 11.7214
90; 90; 120		2555Bandar, Jeffrey S.; Barthelme, Alexandre P.; Mazori, Alon Y.; Lambert, Tristan H.
Structure-Activity Relationship Studies of Cyclopropenimines as Enantioselective Brønsted Base Catalysts.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 1537-1547
1518453 CIFC32 H31 F3 N4 O6I 41/a28.1062; 28.1062; 14.709
90; 90; 90		11619.5Jiao, Wei-Hua; Chen, Guo-Dong; Gao, Hao; Li, Jing; Gu, Bin-Bin; Xu, Ting-Ting; Yu, Hao-Bing; Shi, Guo-Hua; Yang, Fan; Yao, Xin-Sheng; Lin, Hou-Wen
(±)-Quassidines I and J, Two Pairs of Cytotoxic Bis-β-carboline Alkaloid Enantiomers from Picrasma quassioides.
Journal of natural products, 2015, 78, 125-130
1518454 CIFC11 H18 N8 O3P m n 219.5289; 9.1191; 8.667
90; 90; 90		753.12Gryl, Marlena; Cenedese, Simone; Stadnicka, Katarzyna
Crystal Engineering and Charge Density Study of Pharmaceutical Nonlinear Optical Material: Melamine-Barbital Co-Crystal
The Journal of Physical Chemistry C, 2015, 119, 590
1518455 CIFC29 H37 N3 O4P 21 21 217.788; 16.0615; 20.7023
90; 90; 90		2589.6Lee, Pin-Sheng; Yoshikai, Naohiko
Cobalt-catalyzed enantioselective directed C-h alkylation of indole with styrenes.
Organic letters, 2015, 17, 22-25
1518456 CIFC21 H28 O4 SC 1 2 119.3925; 6.0017; 17.9993
90; 107.635; 90		1996.45Lan, Ping; Banwell, Martin G.; Willis, Anthony C.
Chemoenzymatic Synthesis of the Enantiomer of 4,12-Dihydroxysterpurene, the Structure Assigned to a Metabolite Isolated from the Culture Broth of Stereum purpureum.
Organic letters, 2015, 17, 166-169
1518457 CIFC21 H28 O4P 21 21 216.2688; 16.308; 18.2849
90; 90; 90		1869.29Lan, Ping; Banwell, Martin G.; Willis, Anthony C.
Chemoenzymatic Synthesis of the Enantiomer of 4,12-Dihydroxysterpurene, the Structure Assigned to a Metabolite Isolated from the Culture Broth of Stereum purpureum.
Organic letters, 2015, 17, 166-169
1518458 CIFC24 H25 N O5P 21 21 219.0419; 12.2803; 19.0748
90; 90; 90		2118.01Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong
Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.
Organic letters, 2015, 17, 150-153
1518459 CIFC24 H23 N O4P 1 21/c 19.6257; 24.6776; 9.1983
90; 108.936; 90		2066.71Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong
Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.
Organic letters, 2015, 17, 150-153
1518460 CIFC25 H25 N O4P -110.1067; 11.5787; 19.2079
83.811; 82.159; 76.354		2157.2Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong
Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.
Organic letters, 2015, 17, 150-153
1518461 CIFC24 H21 Cl2 N O4C 1 2 121.3083; 16.6395; 17.8923
90; 118.967; 90		5550.3Liu, Ze-Shui; Li, Wen-Ke; Kang, Tai-Ran; He, Long; Liu, Quan-Zhong
Palladium-catalyzed asymmetric cycloadditions of vinylcyclopropanes and in situ formed unsaturated imines: construction of structurally and optically enriched spiroindolenines.
Organic letters, 2015, 17, 150-153
1518462 CIFC21 H21 Br N2 O3 SP c a 2124.0183; 11.2598; 7.4174
90; 90; 90		2005.97Arai, Noriyoshi; Mizota, Moe; Ohkuma, Takeshi
Stereoselective preparation of spiro[4.4] cyclic compounds by the photochemical activation of oxazoles.
Organic letters, 2015, 17, 86-89
1518463 CIFC21 H21 Br N2 O3 SP 1 21/n 18.12; 11.101; 21.7055
90; 94.955; 90		1949.2Arai, Noriyoshi; Mizota, Moe; Ohkuma, Takeshi
Stereoselective preparation of spiro[4.4] cyclic compounds by the photochemical activation of oxazoles.
Organic letters, 2015, 17, 86-89
1518464 CIFC19 H26 O7P 21 21 219.1452; 12.5627; 16.2841
90; 90; 90		1870.85Xu, Jin-Fang; Zhao, Hui-Jun; Wang, Xiao-Bing; Li, Zhong-Rui; Luo, Jun; Yang, Ming-Hua; Yang, Lei; Yu, Wen-Ying; Yao, He-Quan; Luo, Jian-Guang; Kong, Ling-Yi
(±)-Melicolones A and B, Rearranged Prenylated Acetophenone Stereoisomers with an Unusual 9-Oxatricyclo[3.2.1.1(3,8)]nonane Core from the Leaves of Melicope ptelefolia.
Organic letters, 2015, 17, 146-149
1518465 CIFC19 H26 O7P 329.2683; 9.2683; 18.5901
90; 90; 120		1382.97Xu, Jin-Fang; Zhao, Hui-Jun; Wang, Xiao-Bing; Li, Zhong-Rui; Luo, Jun; Yang, Ming-Hua; Yang, Lei; Yu, Wen-Ying; Yao, He-Quan; Luo, Jian-Guang; Kong, Ling-Yi
(±)-Melicolones A and B, Rearranged Prenylated Acetophenone Stereoisomers with an Unusual 9-Oxatricyclo[3.2.1.1(3,8)]nonane Core from the Leaves of Melicope ptelefolia.
Organic letters, 2015, 17, 146-149
1518466 CIFC24.5 H26.52 O7C 1 2 143.491; 5.5109; 18.3225
90; 95.331; 90		4372.4McDonald, Benjamin R.; Nibbs, Antoinette E.; Scheidt, Karl A.
A biomimetic strategy to access the silybins: total synthesis of (-)-isosilybin a.
Organic letters, 2015, 17, 98-101
1518467 CIFC18 H26 O4P -17.1391; 7.5445; 15.455
88.709; 83.268; 76.661		804.4Suizu, Hiroshi; Shigeoka, Daisuke; Aoyama, Hiroshi; Yoshimitsu, Takehiko
Total synthesis of clavilactone B: a radical cyclization-fragmentation strategy.
Organic letters, 2015, 17, 126-129
1518468 CIFC19 H24 O7 SP 1 21/n 116.194; 6.597; 18.175
90; 102.603; 90		1894.9Suizu, Hiroshi; Shigeoka, Daisuke; Aoyama, Hiroshi; Yoshimitsu, Takehiko
Total synthesis of clavilactone B: a radical cyclization-fragmentation strategy.
Organic letters, 2015, 17, 126-129
1518469 CIFC21 H10 Au B Cl10 N6 PbP -18.5794; 13.7444; 13.7913
110.805; 93.371; 101.13		1477.17Echeverría, Raquel; López-de-Luzuriaga, José M.; Monge, Miguel; Olmos, M. Elena
The gold(i)⋯lead(ii) interaction: a relativistic connection
Chem. Sci., 2015, 6, 2022
1518470 CIFC18 H21 N3 O13P 1 21/c 110.0519; 11.0764; 19.917
90; 115.105; 90		2008Ivanova, B.; Spiteller, M.
Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil
Environmental Geochemistry and Health, 2015
1518471 CIFC8 H15 N2 O3P 1 21/n 18.504; 11.8666; 9.5595
90; 96.868; 90		957.8Ivanova, B.; Spiteller, M.
Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil
Environmental Geochemistry and Health, 2015
1518472 CIFC9 H17 N2 O2P 1 21/c 110.928; 6.85; 14.18
90; 91.265; 90		1061.2Ivanova, B.; Spiteller, M.
Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil
Environmental Geochemistry and Health, 2015
1518473 CIFC28 H27 N4 O16C 1 2/c 117.65; 7.5376; 22.793
90; 91.608; 90		3031.2Ivanova, B.; Spiteller, M.
Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil
Environmental Geochemistry and Health, 2015
1518474 CIFC8 H15 N2 O3P 1 21/c 110.028; 9.435; 11.76
90; 122.95; 90		934Ivanova, B.; Spiteller, M.
Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil
Environmental Geochemistry and Health, 2015
1518475 CIFC19 H22 N2 O13P 1 21/n 19.975; 11.085; 18.066
90; 94.823; 90		1990.5Ivanova, B.; Spiteller, M.
Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil
Environmental Geochemistry and Health, 2015
1518476 CIFC14 H23 F6 O6 Pd SbP -19.539; 10.408; 11.253
115.767; 97.422; 91.945		992.6Commarieu, Basile; Claverie, Jerome P.
Bypassing the lack of reactivity of endo-substituted norbornenes with the catalytic rectification‒insertion mechanism
Chem. Sci., 2015, 6, 2172
1518477 CIFC15 H22 F6 N O6 Pd SbP n m a18.89; 16.805; 13.196
90; 90; 90		4189Commarieu, Basile; Claverie, Jerome P.
Bypassing the lack of reactivity of endo-substituted norbornenes with the catalytic rectification‒insertion mechanism
Chem. Sci., 2015, 6, 2172
1518478 CIFC22 H35 F6 O6 Pd SbP n a 2116.758; 16.947; 9.5046
90; 90; 90		2699.3Commarieu, Basile; Claverie, Jerome P.
Bypassing the lack of reactivity of endo-substituted norbornenes with the catalytic rectification–insertion mechanism
Chem. Sci., 2015, 6, 2172
1518479 CIFC17 H28 F6 N3 O10 Pd SbP 1 21/c 110.0271; 19.0026; 14.5138
90; 92.747; 90		2762.3Commarieu, Basile; Claverie, Jerome P.
Bypassing the lack of reactivity of endo-substituted norbornenes with the catalytic rectification‒insertion mechanism
Chem. Sci., 2015, 6, 2172
1518480 CIFC66 H86 Cl20 F24 O16 Pd4 Sb4P -116.4284; 19.3745; 21.4447
66.181; 88.434; 72.775		5930.9Commarieu, Basile; Claverie, Jerome P.
Bypassing the lack of reactivity of endo-substituted norbornenes with the catalytic rectification‒insertion mechanism
Chem. Sci., 2015, 6, 2172
1518481 CIFC12 H15 Cl O6P 1 21 14.6451; 11.3065; 12.3885
90; 94.458; 90		648.67Wu, Jing; Tokunaga, Taiki; Kondo, Mitsuru; Ishigami, Kota; Tokuyama, Shinji; Suzuki, Tomohiro; Choi, Jae-Hoon; Hirai, Hirofumi; Kawagishi, Hirokazu
Erinaceolactones A to C, from the Culture Broth of Hericium erinaceus.
Journal of natural products, 2015, 78, 155-158
1518482 CIFC24 H20 N2 OP b c a8.8127; 13.2298; 32.5
90; 90; 90		3789.2Fan, Zhoulong; Song, Shanshan; Li, Wei; Geng, Kaijun; Xu, Youjun; Miao, Ze-Hong; Zhang, Ao
Rh(III)-Catalyzed Redox-Neutral C-H Activation of Pyrazolones: An Economical Approach for the Synthesis of N-Substituted Indoles.
Organic letters, 2015, 17, 310-313
1518483 CIFC23 H24 Cl N O4P -110.0098; 10.1777; 12.0505
67.347; 70.617; 79.738		1066.95Craig, Alexander J.; van der Salm, Louise; Stevens-Cullinane, Lars; Lucas, Nigel T.; Tan, Eng Wui; Hawkins, Bill C.
Expedient Metal-Free Synthesis of 1,3-Oxazinen-4-ones.
Organic letters, 2015, 17, 234-237
1518484 CIFC54 H75 N8 O16 SP 19.1948; 12.5947; 13.668
79.379; 77.83; 78.547		1499.6Ganesh Kumar, Mothukuri; Mali, Sachitanand M.; Raja, K. Muruga Poopathi; Gopi, Hosahudya N.
Design of Stable β-Hairpin Mimetics through Backbone Disulfide Bonds.
Organic letters, 2015, 17, 230-233
1518485 CIFC22 H16 I N O2 SP 1 21/c 18.0428; 19.587; 12.8121
90; 104.921; 90		1950.29Sun, Lang; Zhu, Yuanxun; Wang, Jing; Lu, Ping; Wang, Yanguang
Lewis Acid Catalyzed Cascade Reaction of 3-(2-Benzenesulfonamide)propargylic Alcohols to Spiro[indene-benzosultam]s.
Organic letters, 2015, 17, 242-245
1518486 CIFC21 H14 I N O2 SP -18.195; 10.1773; 11.9407
86.942; 83.912; 76.661		963.13Sun, Lang; Zhu, Yuanxun; Wang, Jing; Lu, Ping; Wang, Yanguang
Lewis Acid Catalyzed Cascade Reaction of 3-(2-Benzenesulfonamide)propargylic Alcohols to Spiro[indene-benzosultam]s.
Organic letters, 2015, 17, 242-245
1518487 CIFC24 H24 O6C 1 c 117.142; 9.0363; 12.653
90; 90.03; 90		1960Zhang, Junhui; Xing, Siyang; Ren, Jun; Jiang, Shende; Wang, Zhongwen
Lewis Acid catalyzed intramolecular [3 + 2] cross cycloadditions of cobalt-alkynylcyclopropane 1,1-diesters with carbonyls for construction of medium-sized and polycyclic skeletons.
Organic letters, 2015, 17, 218-221
1518488 CIFC16 H16 O5P n a 2114.969; 7.307; 12.761
90; 90; 90		1395.8Zhang, Junhui; Xing, Siyang; Ren, Jun; Jiang, Shende; Wang, Zhongwen
Lewis Acid catalyzed intramolecular [3 + 2] cross cycloadditions of cobalt-alkynylcyclopropane 1,1-diesters with carbonyls for construction of medium-sized and polycyclic skeletons.
Organic letters, 2015, 17, 218-221
1518489 CIFC22 H14 Co2 O11P -18.0572; 8.3258; 17.63
88.79; 84.64; 75.45		1139.7Zhang, Junhui; Xing, Siyang; Ren, Jun; Jiang, Shende; Wang, Zhongwen
Lewis Acid catalyzed intramolecular [3 + 2] cross cycloadditions of cobalt-alkynylcyclopropane 1,1-diesters with carbonyls for construction of medium-sized and polycyclic skeletons.
Organic letters, 2015, 17, 218-221
1518490 CIFC36 H34 Co2 F6 N O5 P2P 21 21 215.8829; 19.5684; 11.5831
90; 90; 90		3600.1Orgué, Sílvia; León, Thierry; Riera, Antoni; Verdaguer, Xavier
Asymmetric Intermolecular Cobalt-Catalyzed Pauson-Khand Reaction Using a P-Stereogenic Bis-phosphane.
Organic letters, 2015, 17, 250-253
1518491 CIFC30 H37 Co2 N3 O5 P2 SiP 1 21 18.8649; 20.8055; 9.1083
90; 101.487; 90		1646.3Orgué, Sílvia; León, Thierry; Riera, Antoni; Verdaguer, Xavier
Asymmetric Intermolecular Cobalt-Catalyzed Pauson-Khand Reaction Using a P-Stereogenic Bis-phosphane.
Organic letters, 2015, 17, 250-253
1518492 CIFC32 H22 B Cl3 F4 N2 O2C 1 2/c 130.8526; 11.997; 18.7562
90; 113.744; 90		6354.75Greulich, Tobias W.; Daniliuc, Constantin G.; Studer, Armido
N-aminopyridinium salts as precursors for N-centered radicals - direct amidation of arenes and heteroarenes.
Organic letters, 2015, 17, 254-257
1518493 CIFC15 H10 Cl N O3P 1 21/n 18.5347; 14.9824; 10.2813
90; 96.632; 90		1305.88Greulich, Tobias W.; Daniliuc, Constantin G.; Studer, Armido
N-aminopyridinium salts as precursors for N-centered radicals - direct amidation of arenes and heteroarenes.
Organic letters, 2015, 17, 254-257
1518494 CIFC18 H20 N2 O2 SP c a 2112.7796; 13.8018; 18.4448
90; 90; 90		3253.32Greulich, Tobias W.; Daniliuc, Constantin G.; Studer, Armido
N-aminopyridinium salts as precursors for N-centered radicals - direct amidation of arenes and heteroarenes.
Organic letters, 2015, 17, 254-257
1518495 CIFC16 H12 Br N3P 3210.18; 10.18; 10.954
90; 90; 120		983.1Tang, Hai-Tao; Xiong, Kai; Li, Ren-Hao; Ding, Zong-Cang; Zhan, Zhuang-Ping
Synthesis of 5,6-Dihydropyrazolo[1,5-c]quinazolines through Gold-Catalyzed Chemoselective Bicyclization of N-Propargylic Sulfonylhydrazones.
Organic letters, 2015, 17, 326-329
1518496 CIFC34 H58 As4 Co2P 1 21/n 18.4386; 13.7676; 16.0276
90; 100.27; 90		1832.24Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518497 CIFC35 H60 As4 Cl2 Co2C 1 2/c 117.893; 19.9249; 11.6299
90; 107.903; 90		3945.5Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518498 CIFC68 H116 As10 Co4P -110.3921; 14.3707; 14.8262
62.53; 76.535; 79.819		1904.35Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518499 CIFC72 H124 As10 Cl8 Co4P -113.7956; 14.0892; 15.0382
62.971; 69.895; 61.292		2254Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518500 CIFC51 H87 As12 Co3C 1 2/c 128.9202; 15.7899; 29.9375
90; 112.752; 90		12607.1Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M.
Synthesis of arsenic-rich Asnligand complexes from yellow arsenic
Chem. Sci., 2015, 6, 1379
1518501 CIFC23 H32 N2 SeP n a 2123.3; 7.0807; 11.6415
90; 90; 90		1920.6Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518502 CIFC15 H24 N2 SeP 1 21/c 111.8147; 11.1443; 12.2088
90; 108.21; 90		1527Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518503 CIFC27 H48 N2 SeP 1 21/n 114.4058; 7.4133; 25.023
90; 97.856; 90		2647.2Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518504 CIFC19 H20 N2 SeP 1 2/n 18.3318; 7.4265; 13.6459
90; 98.798; 90		834.42Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518505 CIFC21 H24 N2 SeP b c n16.043; 7.3937; 16.055
90; 90; 90		1904.4Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518506 CIFC35 H52 N2 SeP 1 21/c 120.433; 7.6327; 21.563
90; 106.66; 90		3221.8Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518507 CIFC27 H34 Cl2 N2 SeI 1 2/a 117.366; 9.4565; 21.295
90; 109.08; 90		3305Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518508 CIFC21 H26 N2 SeP b c n15.9194; 7.4418; 16.1915
90; 90; 90		1918.2Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518509 CIFC11 H6 F5 N3 SeP 1 21/c 19.3746; 15.527; 8.3524
90; 90.357; 90		1215.7Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518510 CIFC11 H11 N3 O SeP -17.8283; 7.9731; 18.447
97.93; 94.637; 90.042		1136.6Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518511 CIFC21 H21 N3 O SeP -18.5326; 10.637; 11.589
107.558; 101.546; 107.498		906.2Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518512 CIFC30 H35 N3 O Se SiP b c a13.2692; 19.8926; 20.979
90; 90; 90		5537.6Vummaleti, Sai V. C.; Nelson, David J.; Poater, Albert; Gómez-Suárez, Adrián; Cordes, David B.; Slawin, Alexandra M. Z.; Nolan, Steven P.; Cavallo, Luigi
What can NMR spectroscopy of selenoureas and phosphinidenes teach us about the π-accepting abilities of N-heterocyclic carbenes?
Chem. Sci., 2015, 6, 1895
1518513 CIFC28 H22 N2 O2P 1 21/c 18.61; 12.78; 20.458
90; 101.72; 90		2204.2Asiri, Abdullah M.; Heller, Harry G.; Hughes, David S.; Hursthouse, Michael B.; Kendrick, John; Leusen, Frank Jj; Montis, Riccardo
A mechanophysical phase transition provides a dramatic example of colour polymorphism: the tribochromism of a substituted tri(methylene)tetrahydrofuran-2-one.
Chemistry Central journal, 2014, 8, 70
1518514 CIFC25 H18 N2 O2P 1 21/n 114.384; 8.214; 17.365
90; 105.53; 90		1976.77Asiri, Abdullah M.; Heller, Harry G.; Hughes, David S.; Hursthouse, Michael B.; Kendrick, John; Leusen, Frank Jj; Montis, Riccardo
A mechanophysical phase transition provides a dramatic example of colour polymorphism: the tribochromism of a substituted tri(methylene)tetrahydrofuran-2-one.
Chemistry Central journal, 2014, 8, 70
1518515 CIFC27 H20 N2 O2P 1 21/c 110.07; 23.91; 9.5
90; 110.38; 90		2144Asiri, Abdullah M.; Heller, Harry G.; Hughes, David S.; Hursthouse, Michael B.; Kendrick, John; Leusen, Frank Jj; Montis, Riccardo
A mechanophysical phase transition provides a dramatic example of colour polymorphism: the tribochromism of a substituted tri(methylene)tetrahydrofuran-2-one.
Chemistry Central journal, 2014, 8, 70
1518516 CIFC27 H20 N2 O2C 1 2/c 120.349; 10.095; 21.338
90; 99.06; 90		4328.6Asiri, Abdullah M.; Heller, Harry G.; Hughes, David S.; Hursthouse, Michael B.; Kendrick, John; Leusen, Frank Jj; Montis, Riccardo
A mechanophysical phase transition provides a dramatic example of colour polymorphism: the tribochromism of a substituted tri(methylene)tetrahydrofuran-2-one.
Chemistry Central journal, 2014, 8, 70
1518517 CIFC23 H16 N2 O2P 1 21 110.352; 7.212; 13.32
90; 110.332; 90		932.49Asiri, Abdullah M.; Heller, Harry G.; Hughes, David S.; Hursthouse, Michael B.; Kendrick, John; Leusen, Frank Jj; Montis, Riccardo
A mechanophysical phase transition provides a dramatic example of colour polymorphism: the tribochromism of a substituted tri(methylene)tetrahydrofuran-2-one.
Chemistry Central journal, 2014, 8, 70
1518518 CIFC21 H25 Cl2 Fe N O Pt SP 21 21 2111.167; 13.257; 14.878
90; 90; 90		2202.6López, Concepción; Bosque, Ramón; Pujol, Marta; Simó, Jonathan; Sevilla, Eila; Font-Bardía, Mercè; Messeguer, Ramon; Calvis, Carme
Experimental and Theoretical Studies of the Factors Affecting the Cycloplatination of the Chiral Ferrocenylaldimine (SC)-[(η5-C5H5)Fe{(η5-C5H4)‒C(H)=N‒CH(Me)(C6H5)}]
Inorganics, 2014, 2, 620
1518519 CIFC144 H104 Au8 F24 Mo12 O46 P8 SiP -116.296; 16.357; 16.854
77.37; 75.89; 80.58		4222.5Yoshida, Takuya; Yasuda, Yuta; Nagashima, Eri; Arai, Hidekazu; Matsunaga, Satoshi; Nomiya, Kenji
Various Oxygen-Centered Phosphanegold(I) Cluster Cations Formed by Polyoxometalate (POM)-Mediated Clusterization: Effects of POMs and Phosphanes
Inorganics, 2014, 2, 660
1518520 CIFC168 H168 Au8 O46 P8 Si W12R -3 :H20.478; 20.478; 36.726
90; 90; 120		13338Yoshida, Takuya; Yasuda, Yuta; Nagashima, Eri; Arai, Hidekazu; Matsunaga, Satoshi; Nomiya, Kenji
Various Oxygen-Centered Phosphanegold(I) Cluster Cations Formed by Polyoxometalate (POM)-Mediated Clusterization: Effects of POMs and Phosphanes
Inorganics, 2014, 2, 660
1518521 CIFC168 H168 Au8 Mo12 O46 P8 SiR -3 :H20.3813; 20.3813; 36.679
90; 90; 120		13195.1Yoshida, Takuya; Yasuda, Yuta; Nagashima, Eri; Arai, Hidekazu; Matsunaga, Satoshi; Nomiya, Kenji
Various Oxygen-Centered Phosphanegold(I) Cluster Cations Formed by Polyoxometalate (POM)-Mediated Clusterization: Effects of POMs and Phosphanes
Inorganics, 2014, 2, 660
1518522 CIFC108 H73 Au6 F18 Mo12 O42 P7P -116.191; 29.165; 35.365
99.801; 99.153; 104.963		15532Yoshida, Takuya; Yasuda, Yuta; Nagashima, Eri; Arai, Hidekazu; Matsunaga, Satoshi; Nomiya, Kenji
Various Oxygen-Centered Phosphanegold(I) Cluster Cations Formed by Polyoxometalate (POM)-Mediated Clusterization: Effects of POMs and Phosphanes
Inorganics, 2014, 2, 660
1518523 CIFC147 H147 Au7 O42 P8 W12P -117.7243; 17.8341; 31.757
104.826; 92.64; 109.685		9040Yoshida, Takuya; Yasuda, Yuta; Nagashima, Eri; Arai, Hidekazu; Matsunaga, Satoshi; Nomiya, Kenji
Various Oxygen-Centered Phosphanegold(I) Cluster Cations Formed by Polyoxometalate (POM)-Mediated Clusterization: Effects of POMs and Phosphanes
Inorganics, 2014, 2, 660
1518524 CIFC24 H26 Cl2 N4 S4 SnC 1 2/c 131.03; 7.961; 11.718
90; 97.377; 90		2871Burkett, Eon; Siddiquee, Tasneem
Coordination Nature of 4-Mercaptoaniline to Sn(II) Ion: Formation of a One Dimensional Coordination Polymer and Its Decomposition to a Mono Nuclear Sn(IV) Complex
Inorganics, 2014, 2, 652
1518525 CIFC12 H15 Cl N2 O S2 SnP 1 21/c 117.328; 12.16; 7.253
90; 95.404; 90		1521Burkett, Eon; Siddiquee, Tasneem
Coordination Nature of 4-Mercaptoaniline to Sn(II) Ion: Formation of a One Dimensional Coordination Polymer and Its Decomposition to a Mono Nuclear Sn(IV) Complex
Inorganics, 2014, 2, 652
1518526 CIFC12 H11 N O2P -14.00444; 11.1381; 12.202
71.955; 89.514; 80.992		510.62Surampudi, S.; Yeh, M.-L.; Siegler, M. A.; Hardigree, J. F. Martinez; Kasl, T. A.; Katz, H. E.; Klausen, R. S.
Increased carrier mobility in end-functionalized oligosilanes
Chem. Sci., 2015, 6, 1905
1518527 CIFC38 H48 N2 O4P 1 21/c 114.93217; 14.22602; 15.93712
90; 100.89; 90		3324.49Surampudi, S.; Yeh, M.-L.; Siegler, M. A.; Hardigree, J. F. Martinez; Kasl, T. A.; Katz, H. E.; Klausen, R. S.
Increased carrier mobility in end-functionalized oligosilanes
Chem. Sci., 2015, 6, 1905
1518528 CIFC30 H40 N2 O4 Si4P -18.5558; 11.887; 17.0071
99.115; 92.129; 94.397		1700.67Surampudi, S.; Yeh, M.-L.; Siegler, M. A.; Hardigree, J. F. Martinez; Kasl, T. A.; Katz, H. E.; Klausen, R. S.
Increased carrier mobility in end-functionalized oligosilanes
Chem. Sci., 2015, 6, 1905
1518529 CIFC34 H52 N2 O4 Si6P -18.6514; 11.8373; 20.4256
82.751; 87.339; 86.175		2068.9Surampudi, S.; Yeh, M.-L.; Siegler, M. A.; Hardigree, J. F. Martinez; Kasl, T. A.; Katz, H. E.; Klausen, R. S.
Increased carrier mobility in end-functionalized oligosilanes
Chem. Sci., 2015, 6, 1905
1518530 CIFC152.05 H75.74 Cl2.21 F40 N12 S8P -118.9073; 20.7452; 21.091
67.38; 77.21; 65.257		6917.2Mori, Hirotaka; Suzuki, Masaaki; Kim, Woojae; Lim, Jong Min; Kim, Dongho; Osuka, Atsuhiro
5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents
Chem. Sci., 2015, 6, 1696
1518531 CIFC87.05 H40.13 Cl3.96 F20 N6 S6C 1 2/c 149.998; 12.402; 35.242
90; 131.613; 90		16338Mori, Hirotaka; Suzuki, Masaaki; Kim, Woojae; Lim, Jong Min; Kim, Dongho; Osuka, Atsuhiro
5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents
Chem. Sci., 2015, 6, 1696
1518532 CIFC95.3 H48 Cl2.3 F20 N6 O0.5 S8P -117.2734; 18.9028; 30.1289
105; 92.92; 107.23		8989Mori, Hirotaka; Suzuki, Masaaki; Kim, Woojae; Lim, Jong Min; Kim, Dongho; Osuka, Atsuhiro
5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents
Chem. Sci., 2015, 6, 1696
1518533 CIFC90 H72 Ag12 F18 N6 O12 S6R -3 :H23.9571; 23.9571; 16.5415
90; 90; 120		8221.9Xu, Qing-Qing; Dong, Xi-Yan; Huang, Ren-Wu; Li, Bo; Zang, Shuang-Quan; Mak, Thomas C. W.
A thermochromic silver nanocluster exhibiting dual emission character.
Nanoscale, 2015, 7, 1650-1654
1518534 CIFC6 H4 F9 N3 O3 SP 1 21/n 15.2742; 8.2719; 29.673
90; 93.124; 90		1292.64Luo, Jiangshui; Jensen, Annemette H.; Brooks, Neil R.; Sniekers, Jeroen; Knipper, Martin; Aili, David; Li, Qingfeng; Vanroy, Bram; Wübbenhorst, Michael; Yan, Feng; Van Meervelt, Luc; Shao, Zhigang; Fang, Jianhua; Luo, Zheng-Hong; De Vos, Dirk E.; Binnemans, Koen; Fransaer, Jan
1,2,4-Triazolium perfluorobutanesulfonate as an archetypal pure protic organic ionic plastic crystal electrolyte for all-solid-state fuel cells
Energy Environ. Sci., 2015, 8, 1276
1518535 CIFC6 H4 F9 N3 O3 SP 1 21/n 15.351; 8.2492; 30.2383
90; 93.95; 90		1331.59Luo, Jiangshui; Jensen, Annemette H.; Brooks, Neil R.; Sniekers, Jeroen; Knipper, Martin; Aili, David; Li, Qingfeng; Vanroy, Bram; Wübbenhorst, Michael; Yan, Feng; Van Meervelt, Luc; Shao, Zhigang; Fang, Jianhua; Luo, Zheng-Hong; De Vos, Dirk E.; Binnemans, Koen; Fransaer, Jan
1,2,4-Triazolium perfluorobutanesulfonate as an archetypal pure protic organic ionic plastic crystal electrolyte for all-solid-state fuel cells
Energy Environ. Sci., 2015, 8, 1276
1518536 CIFC18 H11 F6 N O3C 1 2/c 132.403; 6.8959; 15.25
90; 97.03; 90		3382Lu, Yi; Wang, Huai-Wei; Spangler, Jillian E.; Chen, Kai; Cui, Pei-Pei; Zhao, Yue; Sun, Wei-Yin; Yu, Jin-Quan
Rh(iii)-catalyzed C–H olefination of N-pentafluoroaryl benzamides using air as the sole oxidant
Chem. Sci., 2015, 6, 1923
1518537 CIFC22 H23 Cl3 N4 O2P -17.4245; 13.2237; 24.7183
96.898; 96.177; 90.664		2394.5Fours, Baptiste; Cartigny, Yohann; Petit, Samuel; Coquerel, Gérard
Formation of new polymorphs without any nucleation step. Desolvation of the rimonabant monohydrate: directional crystallisation concomitant to smooth dehydration.
Faraday discussions, 2015, 179, 475-488
1518538 CIFC19 H33 Cl3 Fe N5 O3P -17.2528; 12.6837; 14.9215
106.95; 99.766; 99.208		1261.66Nesterov, Dmytro S.; Nesterova, Oksana V.; Guedes da Silva, M. Fátima C.; Pombeiro, Armando J. L.
Catalytic behaviour of a novel Fe(iii) Schiff base complex in the mild oxidation of cyclohexane
Catal. Sci. Technol., 2015, 5, 1801
1518539 CIFC17 H24 N2 O5C 1 2/c 114.2575; 13.1713; 20.8636
90; 108.856; 90		3707.7Kar, Sudeshna; Tai, Yian
Marked difference in self-assembly, morphology, and cell viability of positional isomeric dipeptides generated by reversal of sequence.
Soft matter, 2015, 11, 1345-1351
1518540 CIFC18 H33 N2 O8 S2P -17.8956; 9.6557; 14.916
77.311; 81.835; 86.214		1097.43Dumitrescu, Dan; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
Adaptive binding and selection of compressed 1,ω-diammonium-alkanes via molecular encapsulation in water
Chem. Sci., 2015, 6, 2079
1518541 CIFC36 H66 N4 O16 S4I 1 2/c 119.4827; 7.7013; 30.1416
90; 101.758; 90		4427.61Dumitrescu, Dan; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
Adaptive binding and selection of compressed 1,ω-diammonium-alkanes via molecular encapsulation in water
Chem. Sci., 2015, 6, 2079
1518542 CIFC28.7552 H49.5104 N8 O14 S4P -19.7673; 9.8143; 10.2046
94.88; 96.822; 95.184		962.76Dumitrescu, Dan; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail
Adaptive binding and selection of compressed 1,ω-diammonium-alkanes via molecular encapsulation in water
Chem. Sci., 2015, 6, 2079
1518543 CIFC58 H76 Mo2 O10P 1 21/c 19.9404; 15.744; 17.7587
90; 100.059; 90		2736.54Brown-Xu, Samantha E; Chisholm, Malcolm H.; Durr, Christopher B.; Spilker, Thomas F.; Young, Philip J.
MM Quadruply Bonded Complexes Supported by Vinylbenzoate Ligands: Synthesis, Characterization, Photophysical Properties and Application as Synthons.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 1780-1791
1518544 CIFC58 H76 Mo2 O10P -19.8343; 11.252; 15.714
107; 105.165; 90.114		1599.14Brown-Xu, Samantha E; Chisholm, Malcolm H.; Durr, Christopher B.; Spilker, Thomas F.; Young, Philip J.
MM Quadruply Bonded Complexes Supported by Vinylbenzoate Ligands: Synthesis, Characterization, Photophysical Properties and Application as Synthons.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 1780-1791
1518545 CIFC14 H34 Cl Mo P3P 21 21 2111.8282; 12.449; 13.6005
90; 90; 90		2002.7Neary, Michelle C.; Parkin, Gerard
Dehydrogenation, disproportionation and transfer hydrogenation reactions of formic acid catalyzed by molybdenum hydride compounds
Chem. Sci., 2015, 6, 1859
1518546 CIFC9 H5 F3 Mo O3P 16.453; 6.544; 6.7851
107.752; 97.132; 107.192		253.356Hauser, Simone A.; Reich, Robert M.; Mink, János; Pöthig, Alexander; Cokoja, Mirza; Kühn, Fritz E.
Influence of structural and electronic properties of organomolybdenum(ii) complexes of the type [CpMo(CO)3R] and [CpMo(O2)(O)R] (R = Cl, CH3, CF3) on the catalytic olefin epoxidation
Catal. Sci. Technol., 2015, 5, 2282
1518547 CIFC6 H5 F3 Mo O3C 1 2/c 120.5911; 6.9325; 12.3919
90; 117.372; 90		1570.87Hauser, Simone A.; Reich, Robert M.; Mink, János; Pöthig, Alexander; Cokoja, Mirza; Kühn, Fritz E.
Influence of structural and electronic properties of organomolybdenum(ii) complexes of the type [CpMo(CO)3R] and [CpMo(O2)(O)R] (R = Cl, CH3, CF3) on the catalytic olefin epoxidation
Catal. Sci. Technol., 2015, 5, 2282
1518548 CIFC44.71 H22.16 Cl4 F14 N6 Na2 O7.22P -114.6741; 15.8676; 24.1918
91.946; 106.327; 115.228		4812.8Seifert, Sabine; Schmidt, David; Würthner, Frank
An ambient stable core-substituted perylene bisimide dianion: isolation and single crystal structure analysis
Chem. Sci., 2015, 6, 1663
1518549 CIFC22 H24 O6P -16.0103; 8.0802; 22.1231
94.344; 93.489; 111.753		990.42Merlani, Maia; Koyama, Yasuhito; Sato, Hiroyasu; Geng, Li; Barbakadze, Vakhtang; Chankvetadze, Bezhan; Nakano, Tamaki
Ring-opening polymerization of a 2,3-disubstituted oxirane leading to a polyether having a carbonyl–aromatic π-stacked structure
Polym. Chem., 2015, 6, 1932
1518550 CIFC20 H18 O5P -19.6559; 9.9869; 18.8822
84.288; 81.394; 73.131		1719.86Merlani, Maia; Koyama, Yasuhito; Sato, Hiroyasu; Geng, Li; Barbakadze, Vakhtang; Chankvetadze, Bezhan; Nakano, Tamaki
Ring-opening polymerization of a 2,3-disubstituted oxirane leading to a polyether having a carbonyl–aromatic π-stacked structure
Polym. Chem., 2015, 6, 1932
1518551 CIFC14 H26 F6 Li N O10 S2P -19.2411; 9.6767; 13.9904
95.234; 97.155; 95.662		1228.46Mandai, Toshihiko; Yoshida, Kazuki; Tsuzuki, Seiji; Nozawa, Risa; Masu, Hyuma; Ueno, Kazuhide; Dokko, Kaoru; Watanabe, Masayoshi
Effect of ionic size on solvate stability of glyme-based solvate ionic liquids.
The journal of physical chemistry. B, 2015, 119, 1523-1534
1518552 CIFC14 H26 F6 K N O10 S2P -19.4304; 16.507; 18.079
66.416; 78.33; 81.019		2517.1Mandai, Toshihiko; Yoshida, Kazuki; Tsuzuki, Seiji; Nozawa, Risa; Masu, Hyuma; Ueno, Kazuhide; Dokko, Kaoru; Watanabe, Masayoshi
Effect of ionic size on solvate stability of glyme-based solvate ionic liquids.
The journal of physical chemistry. B, 2015, 119, 1523-1534
1518553 CIFC10 H16 F6 Li N O8 S2P -18.838; 9.535; 11.379
81.162; 78.012; 79.457		915.5Mandai, Toshihiko; Yoshida, Kazuki; Tsuzuki, Seiji; Nozawa, Risa; Masu, Hyuma; Ueno, Kazuhide; Dokko, Kaoru; Watanabe, Masayoshi
Effect of ionic size on solvate stability of glyme-based solvate ionic liquids.
The journal of physical chemistry. B, 2015, 119, 1523-1534
1518554 CIFC14 H24 F6 K N O10 S2P -18.7544; 8.9026; 9.1253
113.587; 95.75; 106.568		605.85Mandai, Toshihiko; Yoshida, Kazuki; Tsuzuki, Seiji; Nozawa, Risa; Masu, Hyuma; Ueno, Kazuhide; Dokko, Kaoru; Watanabe, Masayoshi
Effect of ionic size on solvate stability of glyme-based solvate ionic liquids.
The journal of physical chemistry. B, 2015, 119, 1523-1534
1518555 CIFC12 H26 F6 K O6 PP b c a15.404; 15.758; 16.51
90; 90; 90		4007.6Mandai, Toshihiko; Yoshida, Kazuki; Tsuzuki, Seiji; Nozawa, Risa; Masu, Hyuma; Ueno, Kazuhide; Dokko, Kaoru; Watanabe, Masayoshi
Effect of ionic size on solvate stability of glyme-based solvate ionic liquids.
The journal of physical chemistry. B, 2015, 119, 1523-1534
1518556 CIFC14 H30 F6 K O7 PP 1 21/c 117.084; 13.183; 20.904
90; 105.027; 90		4547Mandai, Toshihiko; Yoshida, Kazuki; Tsuzuki, Seiji; Nozawa, Risa; Masu, Hyuma; Ueno, Kazuhide; Dokko, Kaoru; Watanabe, Masayoshi
Effect of ionic size on solvate stability of glyme-based solvate ionic liquids.
The journal of physical chemistry. B, 2015, 119, 1523-1534
1518557 CIFC7 H6 I Li O3P -16.65059; 6.89548; 18.4951
81.559; 84.29; 84.975		832.52Endo, Manami; Nakane, Yuta; Takahashi, Kiyonori; Hoshino, Norihisa; Takeda, Takashi; Noro, Shin-Ichiro; Nakamura, Takayoshi; Akutagawa, Tomoyuki
Mesophases and Ionic Conductivities of Simple Organic Salts of M(m-Iodobenzoate) (M = Li(+), Na(+), K(+), Rb(+), and Cs(+)).
The journal of physical chemistry. B, 2015, 119, 1768-1777
1518558 CIFC7 H6 I Na O3P -16.86202; 7.02675; 18.4262
84.11; 82.711; 89.611		876.62Endo, Manami; Nakane, Yuta; Takahashi, Kiyonori; Hoshino, Norihisa; Takeda, Takashi; Noro, Shin-Ichiro; Nakamura, Takayoshi; Akutagawa, Tomoyuki
Mesophases and Ionic Conductivities of Simple Organic Salts of M(m-Iodobenzoate) (M = Li(+), Na(+), K(+), Rb(+), and Cs(+)).
The journal of physical chemistry. B, 2015, 119, 1768-1777
1518559 CIFC7 H5 I K O2.5P -16.3689; 7.4984; 18.6977
83.832; 83.446; 84.606		878.942Endo, Manami; Nakane, Yuta; Takahashi, Kiyonori; Hoshino, Norihisa; Takeda, Takashi; Noro, Shin-Ichiro; Nakamura, Takayoshi; Akutagawa, Tomoyuki
Mesophases and Ionic Conductivities of Simple Organic Salts of M(m-Iodobenzoate) (M = Li(+), Na(+), K(+), Rb(+), and Cs(+)).
The journal of physical chemistry. B, 2015, 119, 1768-1777
1518560 CIFC7 H6 I O3 RbP 1 21/c 119.6879; 4.001; 12.0832
90; 105.805; 90		915.83Endo, Manami; Nakane, Yuta; Takahashi, Kiyonori; Hoshino, Norihisa; Takeda, Takashi; Noro, Shin-Ichiro; Nakamura, Takayoshi; Akutagawa, Tomoyuki
Mesophases and Ionic Conductivities of Simple Organic Salts of M(m-Iodobenzoate) (M = Li(+), Na(+), K(+), Rb(+), and Cs(+)).
The journal of physical chemistry. B, 2015, 119, 1768-1777
1518561 CIFC7 H6 Cs I O3P 1 21/c 119.6351; 4.13863; 12.4789
90; 106.518; 90		972.22Endo, Manami; Nakane, Yuta; Takahashi, Kiyonori; Hoshino, Norihisa; Takeda, Takashi; Noro, Shin-Ichiro; Nakamura, Takayoshi; Akutagawa, Tomoyuki
Mesophases and Ionic Conductivities of Simple Organic Salts of M(m-Iodobenzoate) (M = Li(+), Na(+), K(+), Rb(+), and Cs(+)).
The journal of physical chemistry. B, 2015, 119, 1768-1777
1518562 CIFC30 H23 F3 N2 O2P 1 21/c 112.476; 8.8085; 23.896
90; 103.508; 90		2553.4Jeżewski, Artur; Hammann, Tommy; Cywiński, Piotr J; Gryko, Daniel T.
Optical Behavior of Substituted 4-(2'-Hydroxyphenyl)imidazoles.
The journal of physical chemistry. B, 2015, 119, 2507-2514
1518563 CIFC60 H48 F6 N4 O5P 1 21/n 116.6424; 9.314; 17.808
90; 99.221; 90		2724.7Jeżewski, Artur; Hammann, Tommy; Cywiński, Piotr J; Gryko, Daniel T.
Optical Behavior of Substituted 4-(2'-Hydroxyphenyl)imidazoles.
The journal of physical chemistry. B, 2015, 119, 2507-2514
1518564 CIFC21 H14 Br NP c a 217.6677; 10.2755; 19.816
90; 90; 90		1561.3Dibble, David J.; Umerani, Mehran J.; Mazaheripour, Amir; Park, Young S.; Ziller, Joseph W.; Gorodetsky, Alon A.
An Aza-Diels–Alder Route to Polyquinolines
Macromolecules, 2015, 48, 557
1518565 CIFC24 H23 N O3P -112.483; 12.4917; 14.6608
71.195; 68.259; 69.138		1935.93Oka, Junko; Okamoto, Ryuichi; Noguchi, Keiichi; Tanaka, Ken
Asymmetric dearomatization of 1-aminonaphthalene derivatives by gold-catalyzed intramolecular double C-C bond formation.
Organic letters, 2015, 17, 676-679
1518566 CIFC24 H27 N O3P 1 21/n 113.1285; 8.9817; 17.2111
90; 107.754; 90		1932.8Oka, Junko; Okamoto, Ryuichi; Noguchi, Keiichi; Tanaka, Ken
Asymmetric dearomatization of 1-aminonaphthalene derivatives by gold-catalyzed intramolecular double C-C bond formation.
Organic letters, 2015, 17, 676-679
1518567 CIFC24 H22 Br N O3P 21 21 218.9945; 12.4644; 17.7143
90; 90; 90		1985.97Oka, Junko; Okamoto, Ryuichi; Noguchi, Keiichi; Tanaka, Ken
Asymmetric dearomatization of 1-aminonaphthalene derivatives by gold-catalyzed intramolecular double C-C bond formation.
Organic letters, 2015, 17, 676-679
1518568 CIFC31 H37 N5 O8 SP 1 21 110.9519; 18.6953; 14.864
90; 100.907; 90		2988.4Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.
Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.
Organic letters, 2015, 17, 418-421
1518569 CIFC15 H19 N O2P -16.6977; 8.9166; 11.8671
97.4234; 102.013; 108.163		644.13Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.
Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.
Organic letters, 2015, 17, 418-421
1518570 CIFC13 H15 N O2P 21 21 219.0807; 9.5935; 12.844
90; 90; 90		1118.91Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.
Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.
Organic letters, 2015, 17, 418-421
1518571 CIFC8 H13 N O3P -17.0255; 8.3274; 8.5054
64.8193; 75.8585; 86.3999		436.19Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.
Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.
Organic letters, 2015, 17, 418-421
1518572 CIFC18 H17 N O2C 1 2/c 116.694; 9.6688; 18.2592
90; 101.972; 90		2883.1Scully, Stephen S.; Zheng, Shao-Liang; Wagner, Bridget K.; Schreiber, Stuart L.
Synthesis of Oxazocenones via Gold(I)-Catalyzed 8-Endo-Dig Hydroalkoxylation of Alkynamides.
Organic letters, 2015, 17, 418-421
1518573 CIFC25 H20 N2 O4P 1 21/c 110.359; 8.616; 22.998
90; 98.931; 90		2027.8Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518574 CIFC26 H22 N2 O4P -18.5149; 11.4869; 11.4981
90.53; 111.599; 91.352		1045.17Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518575 CIFC26 H22 N2 O4P 1 21/c 18.1999; 23.636; 10.7112
90; 97.847; 90		2056.5Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518576 CIFC25 H21 N5 O4P n a 2115.0058; 16.0652; 9.235
90; 90; 90		2226.29Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518577 CIFC26 H21 N3 O4 SP 1 21/n 113.7112; 7.9341; 22.1644
90; 101.626; 90		2361.71Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518578 CIFC25 H22 N2 O5P 1 21/n 112.2086; 8.2983; 20.1576
90; 94.952; 90		2034.56Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518579 CIFC25 H19 N3 O4I 41/a :225.4401; 25.4401; 14.9071
90; 90; 90		9647.9Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518580 CIFC25 H19 N3 O4P -18.2122; 14.1107; 17.9598
100.563; 95.565; 90.101		2035.86Kumar, N. N. Bhuvan; Kuznetsov, Dmitry M.; Kutateladze, Andrei G.
Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxadiazoles Provide Direct Access to Versatile Polyheterocyclic Ketopiperazines Containing a Spiro-oxirane Moiety.
Organic letters, 2015, 17, 438-441
1518581 CIFC14 H16 F N O3P 1 21 110.68; 10.806; 12.352
90; 107.01; 90		1363.2Xu, Yan-Shuang; Tang, Yu; Feng, He-Jing; Liu, Ji-Tian; Hsung, Richard P.
A Highly Regio- and Stereoselective Synthesis of α-Fluorinated Imides via Fluorination of Chiral Enamides.
Organic letters, 2015, 17, 572-575
1518582 CIFC17 H14 F N O3P 1 21 16.5754; 10.311; 11.071
90; 95.19; 90		747.5Xu, Yan-Shuang; Tang, Yu; Feng, He-Jing; Liu, Ji-Tian; Hsung, Richard P.
A Highly Regio- and Stereoselective Synthesis of α-Fluorinated Imides via Fluorination of Chiral Enamides.
Organic letters, 2015, 17, 572-575
1518583 CIFC14 H18 O2P 21 21 218.0591; 9.6081; 15.5767
90; 90; 90		1206.14Homs, Anna; Muratore, Michael E.; Echavarren, Antonio M.
Enantioselective Total Synthesis of (-)-Nardoaristolone B via a Gold(I)-Catalyzed Oxidative Cyclization.
Organic letters, 2015, 17, 461-463
1518584 CIFC32 H33 Br N O2 PP 1 21/n 18.4438; 10.9189; 32.745
90; 95.201; 90		3006.6Barrett, Kimberly T.; Miller, Scott J.
Regioselective derivatizations of a tribrominated atropisomeric benzamide scaffold.
Organic letters, 2015, 17, 580-583
1518585 CIFC33 H35 Au Br Cl3 N O2 PP 1 21/n 19.848; 24.3169; 15.0477
90; 104.667; 90		3486.1Barrett, Kimberly T.; Miller, Scott J.
Regioselective derivatizations of a tribrominated atropisomeric benzamide scaffold.
Organic letters, 2015, 17, 580-583
1518586 CIFC60.5 H56 N4 O6C 1 c 116.1723; 24.7158; 24.1251
90; 90.474; 90		9642.7Liu, Lei; Carroll, Patrick J.; Kozlowski, Marisa C.
Vanadium-catalyzed regioselective oxidative coupling of 2-hydroxycarbazoles.
Organic letters, 2015, 17, 508-511
1518587 CIFC56 H92 Cl2 Co2 I2 N4 P4 Ti2P b c a18.6991; 16.4217; 21.8753
90; 90; 90		6717.3Wu, Bing; Bezpalko, Mark W.; Foxman, Bruce M.; Thomas, Christine M.
A heterobimetallic complex featuring a Ti‒Co multiple bond and its application to the reductive coupling of ketones to alkenes
Chem. Sci., 2015, 6, 2044
1518588 CIFC31 H55 Cl Co N2 P3 TiP 1 21/n 19.0138; 18.8395; 21.5085
90; 90.54; 90		3652.3Wu, Bing; Bezpalko, Mark W.; Foxman, Bruce M.; Thomas, Christine M.
A heterobimetallic complex featuring a Ti‒Co multiple bond and its application to the reductive coupling of ketones to alkenes
Chem. Sci., 2015, 6, 2044
1518589 CIFC68 H104 Co2 I2 N4 O2 P4 Ti2P -112.5912; 13.4571; 13.5956
110.682; 94.623; 117.15		1835.07Wu, Bing; Bezpalko, Mark W.; Foxman, Bruce M.; Thomas, Christine M.
A heterobimetallic complex featuring a Ti‒Co multiple bond and its application to the reductive coupling of ketones to alkenes
Chem. Sci., 2015, 6, 2044
1518590 CIFC24 H16 Au2 F8 N4 O2P -13.5452; 14.0087; 14.249
109.292; 91.673; 91.322		667.23Seki, Tomohiro; Ozaki, Taichi; Okura, Takuma; Asakura, Kiyotaka; Sakon, Aya; Uekusa, Hidehiro; Ito, Hajime
Interconvertible multiple photoluminescence color of a gold(i) isocyanide complex in the solid state: solvent-induced blue-shifted and mechano-responsive red-shifted photoluminescence
Chem. Sci., 2015, 6, 2187
1518591 CIFC18 H4 Au2 F8 N4P -13.5707; 10.3087; 14.2742
107.689; 92.505; 100.205		489.99Seki, Tomohiro; Ozaki, Taichi; Okura, Takuma; Asakura, Kiyotaka; Sakon, Aya; Uekusa, Hidehiro; Ito, Hajime
Interconvertible multiple photoluminescence color of a gold(i) isocyanide complex in the solid state: solvent-induced blue-shifted and mechano-responsive red-shifted photoluminescence
Chem. Sci., 2015, 6, 2187
1518592 CIFC18 H4 Au2 F8 N4P 1 21/c 17.79058; 18.7202; 6.74157
90; 103.167; 90		957.35Seki, Tomohiro; Ozaki, Taichi; Okura, Takuma; Asakura, Kiyotaka; Sakon, Aya; Uekusa, Hidehiro; Ito, Hajime
Interconvertible multiple photoluminescence color of a gold(i) isocyanide complex in the solid state: solvent-induced blue-shifted and mechano-responsive red-shifted photoluminescence
Chem. Sci., 2015, 6, 2187
1518593 CIFC30 H51 Ir P2P -110.264; 16.311; 19.425
103.753; 105.008; 93.129		3027.6Polukeev, Alexey V.; Marcos, Rocío; Ahlquist, Mårten S. G.; Wendt, Ola F.
Formation of a C‒C double bond from two aliphatic carbons. Multiple C‒H activations in an iridium pincer complex
Chem. Sci., 2015, 6, 2060
1518594 CIFC31 H55 Ir O P2P 1 21/c 117.003; 20.0591; 9.4403
90; 102.986; 90		3137.41Polukeev, Alexey V.; Marcos, Rocío; Ahlquist, Mårten S. G.; Wendt, Ola F.
Formation of a C‒C double bond from two aliphatic carbons. Multiple C‒H activations in an iridium pincer complex
Chem. Sci., 2015, 6, 2060
1518595 CIFC24 H46 Cl Ir P2P 1 21/c 111.4108; 13.6574; 17.7933
90; 104.097; 90		2689.4Polukeev, Alexey V.; Marcos, Rocío; Ahlquist, Mårten S. G.; Wendt, Ola F.
Formation of a C‒C double bond from two aliphatic carbons. Multiple C‒H activations in an iridium pincer complex
Chem. Sci., 2015, 6, 2060
1518596 CIFC34 H26 F4 P2P 1 21/n 19.2062; 16.7452; 17.6319
90; 101.286; 90		2665.6Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W.
Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
Chem. Sci., 2015, 6, 2016
1518597 CIFC25 H22 F4 P2C 1 2 121.0973; 8.3882; 6.3567
90; 102.383; 90		1098.76Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W.
Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
Chem. Sci., 2015, 6, 2016
1518598 CIFC58 H26 B F21 P2P 1 21 18.4256; 21.123; 13.804
90; 95.055; 90		2447.2Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W.
Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
Chem. Sci., 2015, 6, 2016
1518599 CIFC59.25 H28.5 B Cl2.5 F23 P2P 1 21/c 118.8002; 17.1372; 17.8001
90; 102.564; 90		5597.6Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W.
Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines
Chem. Sci., 2015, 6, 2016
1518604 CIFC23 H38 N2 O2 SiP 21 21 2111.9997; 12.0093; 16.8043
90; 90; 90		2421.63Xu, Xinfang; Deng, Yongming; Yim, David N.; Zavalij, Peter Y.; Doyle, Michael P.
Enantioselective cis-β-lactam synthesis by intramolecular C-H functionalization from enoldiazoacetamides and derivative donor-acceptor cyclopropenes.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 2196-2201
1518605 CIFC83 H82 F24 N12 O5 P4 Ru2P -111.2159; 12.555; 18.1382
70.206; 85.323; 67.45		2216.1Griepenburg, J. C.; Rapp, T. L.; Carroll, P. J.; Eberwine, J.; Dmochowski, I. J.
Ruthenium-Caged Antisense Morpholinos for Regulating Gene Expression in Zebrafish Embryos.
Chemical science (Royal Society of Chemistry : 2010), 2015, 6, 2342-2346
1518606 CIFCl2 O5 Sb4P 1 21/c 16.229; 5.107; 13.5
90; 97.27; 90		426.003Maja Edstrand
On the crystal structure of the antimony oxychloride Sb4O5Cl2 and isomorphous oxybromide
Acta Chemica Scandinavica, 1947, 1, 178-203
1518607 CIFBr2 O5 Sb4P 1 21/c 16.593; 5.133; 13.43
90; 97.89; 90		450.194Maja Edstrand
On the crystal structure of the antimony oxychloride Sb4O5Cl2 and isomorphous oxybromide
Acta Chemica Scandinavica, 1947, 1, 178-203
1518608 CIFNa8 O26 S6 V2P 1 21/c 18.6454; 16.0027; 15.5074
90; 90.017; 90		2145.44Nielsen, Kurt; Boghosian, Soghomon; Fehrmann, Rasmus; Berg, Rolf Willestofte
Crystal Structure and Spectroscopic Characterization of a Green V(IV) Compound, Na8(VO)2(SO4)6
Acta Chemica Scandinavica, 1999, 53, 15-23
1518609 CIFC35 H28 F6 N3 P S2 Se4P 1 21/n 119.6176; 7.5992; 25.2231
90; 93.7263; 90		3752.3Bedics, Matthew A.; Kearns, Hayleigh; Cox, Jordan M.; Mabbott, Sam; Ali, Fatima; Shand, Neil C.; Faulds, Karen; Benedict, Jason B.; Graham, Duncan; Detty, Michael R.
Extreme red shifted SERS nanotags
Chem. Sci., 2015, 6, 2302
1518610 CIFC20 H14P -19.6321; 11.0943; 14.7022
67.862; 79.883; 69.219		1359Collins, Karl D.; Honeker, Roman; Vásquez-Céspedes, Suhelen; Tang, Dan-Tam D.; Glorius, Frank
C–H arylation of triphenylene, naphthalene and related arenes using Pd/C
Chem. Sci., 2015, 6, 1816
1518611 CIFC24 H16P 1 21/c 119.1157; 5.7556; 29.6669
90; 108.002; 90		3104.2Collins, Karl D.; Honeker, Roman; Vásquez-Céspedes, Suhelen; Tang, Dan-Tam D.; Glorius, Frank
C–H arylation of triphenylene, naphthalene and related arenes using Pd/C
Chem. Sci., 2015, 6, 1816
1518612 CIFC27 H36 F2 N P PtP 1 21/n 18.7261; 31.0122; 9.6085
90; 111.319; 90		2422.29Vigalok, Arkadi
Electrophilic halogenation-reductive elimination chemistry of organopalladium and -platinum complexes.
Accounts of chemical research, 2015, 48, 238-247
1518613 CIFC22 H17 N OP 1 21/n 18.8912; 16.859; 11.238
90; 108.555; 90		1597Bunescu, Ala; Piou, Tiffany; Wang, Qian; Zhu, Jieping
Pd-Catalyzed Dehydrogenative Aryl-Aryl Bond Formation via Double C(sp(2))-H Bond Activation: Efficient Synthesis of [3,4]-Fused Oxindoles.
Organic letters, 2015, 17, 334-337
1518614 CIFC22 H16 F N OP 1 21/n 18.922; 16.7585; 11.2263
90; 108.038; 90		1596.05Bunescu, Ala; Piou, Tiffany; Wang, Qian; Zhu, Jieping
Pd-Catalyzed Dehydrogenative Aryl-Aryl Bond Formation via Double C(sp(2))-H Bond Activation: Efficient Synthesis of [3,4]-Fused Oxindoles.
Organic letters, 2015, 17, 334-337
1518615 CIFC52 H50 N4 Ni O2P 1 21/c 118.2078; 16.5273; 14.8317
90; 98.447; 90		4414.8Gehrold, Andreas C.; Bruhn, Torsten; Schneider, Heidi; Radius, Udo; Bringmann, Gerhard
Chiral and achiral basket-handle porphyrins: short synthesis and stereostructures of these versatile building blocks.
Organic letters, 2015, 17, 210-213
1518616 CIFC15 H13 N3C 1 2/c 117.719; 6.475; 22.501
90; 100.868; 90		2535.2Quan, Xue-Jing; Ren, Zhi-Hui; Wang, Yao-Yu; Guan, Zheng-Hui
Correction to p-Toluenesulfonic Acid Mediated 1,3-Dipolar Cycloaddition of Nitroolefins with NaN3 for Synthesis of 4-Aryl-NH-1,2,3-triazoles.
Organic letters, 2015, 17, 393
1518617 CIFC37 H36 Cl2 N4 O8 S2P 21 21 2112.9116; 15.1292; 18.7417
90; 90; 90		3661Liang, Kangjiang; Deng, Xu; Tong, Xiaogang; Li, Dashan; Ding, Ming; Zhou, Ankun; Xia, Chengfeng
Copper-Mediated Dimerization to Access 3a,3a'-Bispyrrolidinoindoline: Diastereoselective Synthesis of (+)-WIN 64821 and (-)-Ditryptophenaline.
Organic letters, 2015, 17, 206-209
1518618 CIFC20 H17 Br N2 OP 19.8359; 10.161; 10.307
76.557; 73.136; 64.754		884.6Fu, Niankai; Zhang, Long; Luo, Sanzhong
Chiral Primary Amine Catalyzed Asymmetric Michael Addition of Malononitrile to α-Substituted Vinyl Ketone.
Organic letters, 2015, 17, 382-385
1518619 CIFC24 H20 N2 OP 21 21 2110.5861; 10.618; 17.0439
90; 90; 90		1915.79Fu, Niankai; Zhang, Long; Luo, Sanzhong
Chiral Primary Amine Catalyzed Asymmetric Michael Addition of Malononitrile to α-Substituted Vinyl Ketone.
Organic letters, 2015, 17, 382-385
1518620 CIFC16 H10 B F2 N3P 1 21/n 19.559; 9.3155; 15.051
90; 102.64; 90		1307.8Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518621 CIFC16 H9 B Cl F2 N3P 1 21/n 17.7337; 19.0699; 9.655
90; 105.059; 90		1375Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518622 CIFC15 H10 B F2 N3 SP 1 21/c 17.9215; 14.0077; 25.071
90; 102.609; 90		2714.8Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518623 CIFC22 H18 B F2 N3 SP -110.092; 10.383; 10.434
65.025; 82.642; 75.499		959.2Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518624 CIFC18 H10 B F2 N3P -17.4838; 9.1552; 11.5629
79.781; 71.778; 67.825		695.26Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518625 CIFC18 H9 B Br F2 N3P -19.1788; 9.5551; 9.9844
87.602; 71.441; 65.179		749.15Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518626 CIFC24 H17 B Br F2 N3 SC 1 2/c 111.3331; 34.017; 12.736
90; 109.159; 90		4638Cheng, Chi; Gao, Naixun; Yu, Changjiang; Wang, Zhaoyun; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Tian, Yanli; Ran, Chongzhao; Jiao, Lijuan
Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes.
Organic letters, 2015, 17, 278-281
1518627 CIFC21 H20 Cl N O3P 1 21/c 115.6314; 21.884; 11.7948
90; 108.565; 90		3824.8Li, Lei; Zhao, Yu-Long; Wang, Qian; Lin, Tao; Liu, Qun
Base-Promoted Oxidative C-H Functionalization of α-Amino Carbonyl Compounds under Mild Metal-Free Conditions: Using Molecular Oxygen as the Oxidant.
Organic letters, 2015, 17, 370-373
1518628 CIFC11 H17 Cl F N O Pt SP 1 21/c 15.9315; 12.1005; 19.7
90; 103.067; 90		1377.34Zamora, Ana; Pérez, Sergio A; Rodríguez, Venancio; Janiak, Christoph; Yellol, Gorakh S.; Ruiz, José
Dual Antitumor and Antiangiogenic Activity of Organoplatinum(II) Complexes.
Journal of medicinal chemistry, 2015, 58, 1320-1336
1518629 CIFC31 H26 Cl F9 N O P PtP 1 21/c 117.3951; 14.9557; 11.9109
90; 98.576; 90		3064Zamora, Ana; Pérez, Sergio A; Rodríguez, Venancio; Janiak, Christoph; Yellol, Gorakh S.; Ruiz, José
Dual Antitumor and Antiangiogenic Activity of Organoplatinum(II) Complexes.
Journal of medicinal chemistry, 2015, 58, 1320-1336
1518630 CIFC34 H38 O8P 21 21 219.67492; 14.41358; 20.6293
90; 90; 90		2876.76Wu, Taizong; Wang, Qian; Jiang, Cheng; Morris-Natschke, Susan L; Cui, Hui; Wang, Yan; Yan, Yuan; Xu, Jun; Lee, Kuo-Hsiung; Gu, Qiong
neo-Clerodane Diterpenoids from Scutellaria barbata with Activity against Epstein-Barr Virus Lytic Replication.
Journal of natural products, 2015, 78, 500-509
1518631 CIFC26 H36 O7P 21 21 219.60332; 9.87431; 26.75
90; 90; 90		2536.6Wu, Taizong; Wang, Qian; Jiang, Cheng; Morris-Natschke, Susan L; Cui, Hui; Wang, Yan; Yan, Yuan; Xu, Jun; Lee, Kuo-Hsiung; Gu, Qiong
neo-Clerodane Diterpenoids from Scutellaria barbata with Activity against Epstein-Barr Virus Lytic Replication.
Journal of natural products, 2015, 78, 500-509
1518632 CIFC15 H22 O3P 21 21 2110.8914; 10.9342; 11.4227
90; 90; 90		1360.32Del Valle, Paulina; Figueroa, Mario; Mata, Rachel
Phytotoxic Eremophilane Sesquiterpenes from the Coprophilous Fungus Penicillium sp. G1-a14.
Journal of natural products, 2015, 78, 339-342
1518633 CIFC24 H17 N OP 1 21/n 19.5489; 9.6991; 19.1473
90; 97.465; 90		1758.31Li, Ziyuan; Huang, Xiaoqiang; Chen, Feng; Zhang, Chun; Wang, Xiaoyang; Jiao, Ning
Cu-Catalyzed Concise Synthesis of Pyridines and 2-(1H)-Pyridones from Acetaldehydes and Simple Nitrogen Donors.
Organic letters, 2015, 17, 584-587
1518634 CIFC20 H22 B F3 K N OP 21 21 216.3906; 7.7434; 38.9797
90; 90; 90		1928.91Hoang, Gia L.; Yang, Zhao-Di; Smith, Sean M.; Pal, Rhitankar; Miska, Judy L.; Pérez, Damaris E; Pelter, Libbie S. W.; Zeng, Xiao Cheng; Takacs, James M.
Enantioselective Desymmetrization via Carbonyl-Directed Catalytic Asymmetric Hydroboration and Suzuki-Miyaura Cross-Coupling.
Organic letters, 2015, 17, 940-943
1518635 CIFC26 H29 B F4 N2 O2P 21 21 218.447; 16.3195; 17.2927
90; 90; 90		2383.8Hoang, Gia L.; Yang, Zhao-Di; Smith, Sean M.; Pal, Rhitankar; Miska, Judy L.; Pérez, Damaris E; Pelter, Libbie S. W.; Zeng, Xiao Cheng; Takacs, James M.
Enantioselective Desymmetrization via Carbonyl-Directed Catalytic Asymmetric Hydroboration and Suzuki-Miyaura Cross-Coupling.
Organic letters, 2015, 17, 940-943
1518636 CIFC46 H44 B3 N3 O7P 1 21/c 116.559; 16.774; 15.989
90; 115.658; 90		4003.2Li, Gang; Xiong, Wei-Wei; Gu, Pei-Yang; Cao, Jun; Zhu, Jia; Ganguly, Rakesh; Li, Yongxin; Grimsdale, Andrew C.; Zhang, Qichun
1,5,9-Triaza-2,6,10-triphenylboracoronene: BN-Embedded Analogue of Coronene.
Organic letters, 2015, 17, 560-563
1518637 CIFC27 H24 B3 N3 O12R -3 :H19.9798; 19.9798; 12.6217
90; 90; 120		4363.46Li, Gang; Xiong, Wei-Wei; Gu, Pei-Yang; Cao, Jun; Zhu, Jia; Ganguly, Rakesh; Li, Yongxin; Grimsdale, Andrew C.; Zhang, Qichun
1,5,9-Triaza-2,6,10-triphenylboracoronene: BN-Embedded Analogue of Coronene.
Organic letters, 2015, 17, 560-563
1518638 CIFC37 H33 B3 Cl3 N3 O7P 1 21/c 113.0661; 12.1247; 22.3242
90; 98.251; 90		3500Li, Gang; Xiong, Wei-Wei; Gu, Pei-Yang; Cao, Jun; Zhu, Jia; Ganguly, Rakesh; Li, Yongxin; Grimsdale, Andrew C.; Zhang, Qichun
1,5,9-Triaza-2,6,10-triphenylboracoronene: BN-Embedded Analogue of Coronene.
Organic letters, 2015, 17, 560-563
1518639 CIFC33 H40 B N O4 SiP 1 21/c 113.3949; 14.3478; 15.283
90; 92.281; 90		2934.9Kubota, Koji; Iwamoto, Hiroaki; Yamamoto, Eiji; Ito, Hajime
Silicon-tethered strategy for copper(i)-catalyzed stereo- and regioselective alkylboration of alkynes.
Organic letters, 2015, 17, 620-623
1518640 CIFC20 H22 N2 O5P -19.272; 15.087; 26.669
75.828; 88.836; 88.885		3616Zhong, Xue; Li, You; Zhang, Jing; Han, Fu-She
Synthetic Study toward the Misassigned (±)-Tronoharine.
Organic letters, 2015, 17, 720-723
1518641 CIFC18 H18 N2 O3P 1 21/n 18.2569; 11.5402; 15.727
90; 102.251; 90		1464.4Zhong, Xue; Li, You; Zhang, Jing; Han, Fu-She
Synthetic Study toward the Misassigned (±)-Tronoharine.
Organic letters, 2015, 17, 720-723
1518642 CIFC13 H12 O3P -19.562; 10.2591; 10.618
87.713; 85.512; 88.206		1037.16Kratochvíl, Jiří; Novák, Zdeněk; Ghavre, Mukund; Nováková, Lucie; R°užička, Aleš; Kuneš, Jiří; Pour, Milan
Fully Substituted Pyranones via Quasi-Heterogeneous Genuinely Ligand-Free Migita-Stille Coupling of Iodoacrylates.
Organic letters, 2015, 17, 520-523
1518643 CIFC21 H18 N2 OP 21 21 218.964; 12.046; 16.315
90; 90; 90		1761.7Manna, Manash Kumar; Hossian, Asik; Jana, Ranjan
Merging C-h activation and alkene difunctionalization at room temperature: a palladium-catalyzed divergent synthesis of indoles and indolines.
Organic letters, 2015, 17, 672-675
1518644 CIFC23 H20 N2 OP -16.345; 11.725; 13.3
67.812; 80.532; 84.005		902.7Manna, Manash Kumar; Hossian, Asik; Jana, Ranjan
Merging C-h activation and alkene difunctionalization at room temperature: a palladium-catalyzed divergent synthesis of indoles and indolines.
Organic letters, 2015, 17, 672-675
1518645 CIFC24 H35 N3 O2P 1 21 112.8948; 9.7854; 18.3889
90; 94.667; 90		2312.6Li, Xun; Taechalertpaisarn, Jaru; Xin, Dongyue; Burgess, Kevin
Protein-Protein Interface Mimicry by an Oxazoline Piperidine-2,4-dione.
Organic letters, 2015, 17, 632-635
1518646 CIFC34 H56 N2 O7 Si2P 21 21 219.052; 19.871; 22.2031
90; 90; 90		3993.72Gazvoda, Martin; Höferl-Prantz, Kathrin; Barth, Roland; Felzmann, Wolfgang; Pevec, Andrej; Košmrlj, Janez
Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids.
Organic letters, 2015, 17, 512-515
1518647 CIFC33 H44 N2 O7 SiP 1 21 118.0919; 10.7097; 18.935
90; 107.979; 90		3489.7Gazvoda, Martin; Höferl-Prantz, Kathrin; Barth, Roland; Felzmann, Wolfgang; Pevec, Andrej; Košmrlj, Janez
Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids.
Organic letters, 2015, 17, 512-515
1518648 CIFC22 H28 N2 O7P 21 21 2111.0538; 12.5835; 15.8359
90; 90; 90		2202.7Gazvoda, Martin; Höferl-Prantz, Kathrin; Barth, Roland; Felzmann, Wolfgang; Pevec, Andrej; Košmrlj, Janez
Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids.
Organic letters, 2015, 17, 512-515
1518649 CIFC17 H17 N O3P 1 21/c 18.9854; 18.5028; 9.4678
90; 109.249; 90		1486.07Ramella, Vincenzo; He, Zhiheng; Daniliuc, Constantin G.; Studer, Armido
Palladium-catalyzed diastereoselective oxyarylation of 2-alkylindoles.
Organic letters, 2015, 17, 664-667
1518650 CIFC25 H22 Cl N O4P -18.5929; 9.9207; 13.6227
73.585; 78.745; 86.593		1092.53Ramella, Vincenzo; He, Zhiheng; Daniliuc, Constantin G.; Studer, Armido
Palladium-catalyzed diastereoselective oxyarylation of 2-alkylindoles.
Organic letters, 2015, 17, 664-667
1518651 CIFC31 H27 N3 O2P 1 21 17.6192; 12.0803; 14.0233
90; 102.158; 90		1261.8Pertejo, Pablo; Corres, Nazaret; Torroba, Tomás; García-Valverde, María
Reversal of Diastereoselectivity in the Synthesis of Peptidomimetic 3-Carboxamide-1,4-benzodiazepin-5-ones.
Organic letters, 2015, 17, 612-615
1518652 CIFC30 H38 N2 O7P 1 21 111.3323; 8.5548; 14.1288
90; 92.453; 90		1368.47Chen, Chunmei; Zhu, Hucheng; Li, Xiao-Nian; Yang, Jing; Wang, Jianping; Li, Gentao; Li, Yan; Tong, Qingyi; Yao, Guangmin; Luo, Zengwei; Xue, Yongbo; Zhang, Yonghui
Armochaeglobines A and B, Two New Indole-Based Alkaloids from the Arthropod-Derived Fungus Chaetomium globosum.
Organic letters, 2015, 17, 644-647
1518653 CIFC32 H40 N2 O7P 1 21 113.4499; 7.46; 14.9726
90; 104.948; 90		1451.46Chen, Chunmei; Zhu, Hucheng; Li, Xiao-Nian; Yang, Jing; Wang, Jianping; Li, Gentao; Li, Yan; Tong, Qingyi; Yao, Guangmin; Luo, Zengwei; Xue, Yongbo; Zhang, Yonghui
Armochaeglobines A and B, Two New Indole-Based Alkaloids from the Arthropod-Derived Fungus Chaetomium globosum.
Organic letters, 2015, 17, 644-647
1518654 CIFC42 H59 F3 O10P 1 21 113.4566; 8.18811; 19.1862
90; 100.629; 90		2077.74Inahashi, Yuki; Iwatsuki, Masato; Ishiyama, Aki; Matsumoto, Atsuko; Hirose, Tomoyasu; Oshita, Jun; Sunazuka, Toshiaki; Panbangred, Watanalai; Takahashi, Yoko; Kaiser, Marcel; Otoguro, Kazuhiko; O̅mura, Satoshi
Actinoallolides A-E, New Anti-trypanosomal Macrolides, Produced by an Endophytic Actinomycete, Actinoallomurus fulvus MK10-036.
Organic letters, 2015, 17, 864-867
1518655 CIFC13 H10 N2 O2 SP 1 21/c 111.9124; 7.5041; 14.67
90; 111.533; 90		1219.9Pawar, Amit B.; Chang, Sukbok
Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent.
Organic letters, 2015, 17, 660-663
1518656 CIFC13 H10 N4 OP -16.9373; 8.2261; 9.7516
85.814; 78.171; 89.197		543.22Pawar, Amit B.; Chang, Sukbok
Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent.
Organic letters, 2015, 17, 660-663
1518657 CIFC14 H11 N5P -17.9667; 8.6666; 9.6847
109.198; 107.554; 92.006		595.36Pawar, Amit B.; Chang, Sukbok
Cobalt-Catalyzed C-H Cyanation of (Hetero)arenes and 6-Arylpurines with N-Cyanosuccinimide as a New Cyanating Agent.
Organic letters, 2015, 17, 660-663
1518658 CIFC16 H19 N O4P 1 21 18.2102; 6.2167; 14.102
90; 90.69; 90		719.7Lou, Yan-Peng; Zheng, Chang-Wu; Pan, Ren-Ming; Jin, Qiao-Wen; Zhao, Gang; Li, Zhong
Enantioselective Direct Mannich Reactions of Cyclic β-Ketoesters Catalyzed by Chiral Phosphine via a Novel Dual-Reagent Catalysis.
Organic letters, 2015, 17, 688-691
1518659 CIFC25 H23 Br O S2 SeP 1 21/c 19.5704; 11.7332; 21.056
90; 97.692; 90		2343.1Wu, Ping; Wang, Liandi; Wu, Kaikai; Yu, Zhengkun
Brønsted Acid Catalyzed PhSe Transfer versus Radical Aryl Transfer: Linear Codimerization of Styrenes and Internal Olefins.
Organic letters, 2015, 17, 868-871
1518660 CIFC20 H21 F O2 S2P 1 21/c 110.5963; 16.7072; 10.9555
90; 95.184; 90		1931.57Wu, Ping; Wang, Liandi; Wu, Kaikai; Yu, Zhengkun
Brønsted Acid Catalyzed PhSe Transfer versus Radical Aryl Transfer: Linear Codimerization of Styrenes and Internal Olefins.
Organic letters, 2015, 17, 868-871
1518661 CIFC64 H48 S4P 1 21/n 120.159; 5.0166; 25.728
90; 109.164; 90		2457.7Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518662 CIFC65 H50 S4P 1 21/n 120.1; 5.1652; 25.159
90; 109.501; 90		2462.2Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518663 CIFC68 H56 Cl2 S4P 1 21/c 17.6706; 17.4871; 20.506
90; 100.272; 90		2706.5Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518664 CIFC66 H52 S4P 1 21/n 121.43; 5.2798; 24.95
90; 111.599; 90		2624.8Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518665 CIFC66 H52 S4P 1 21/n 120.0834; 5.2324; 24.6005
90; 109.019; 90		2444.01Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro
Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations
Chem. Sci., 2015, 6, 2354
1518666 CIFC8 H16 F7 O6 P2 S2 SbP 1 21/n 114.5029; 8.9034; 14.9927
90; 97.26; 90		1920.41Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518667 CIFC43 H71 F9 N3 O9 P3 S3 Sb4P -111.4789; 11.9874; 26.0864
91.82; 97.564; 112.074		3284.57Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518668 CIFC29 H61.5 F12 N0.5 O12 P4 S4 Sb4P 1 21/c 123.986; 21.83; 22.193
90; 106.57; 90		11138Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine–antimony complexes
Chem. Sci., 2015, 6, 2559
1518669 CIFC31 H41 F6 N2 O6 S2 SbP 1 21/c 112.3127; 17.4575; 17.0214
90; 91.03; 90		3658.1Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518670 CIFC4 H9 F4 O3 P SP 1 21/m 110.2147; 8.6511; 11.0323
90; 94.5503; 90		971.83Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine–antimony complexes
Chem. Sci., 2015, 6, 2559
1518671 CIFC14 H30 F6 O6 P2 S2P 1 21/n 113.4271; 11.8532; 15.7504
90; 110.993; 90		2340.4Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland
Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes
Chem. Sci., 2015, 6, 2559
1518672 CIFC27 H24 Cl5 F6 N5 O P2 RuP -111.1445; 12.0548; 14.8726
67.197; 84.942; 67.025		1691.09Walden, Andrew G.; Miller, Alexander J. M.
Rapid water oxidation electrocatalysis by a ruthenium complex of the tripodal ligand tris(2-pyridyl)phosphine oxide
Chem. Sci., 2015, 6, 2405
1518673 CIFC33 H48 N2 O9 SP 1 21 113.6507; 10.3032; 13.9805
90; 109.803; 90		1850.02Shen, Hongyun; Shen, Chao; Chen, Chao; Wang, Anming; Zhang, Pengfei
Novel glycosyl pyridyl-triazole@palladium nanoparticles: efficient and recoverable catalysts for C‒C cross-coupling reactions
Catal. Sci. Technol., 2015, 5, 2065
1518674 CIFC75 H71 Cl2 N3 PdP -112.3155; 15.9288; 19.2346
79.609; 87.992; 81.295		3668.5Maluenda, Irene; Chen, Ming-Tsz; Guest, Daniel; Mark Roe, S.; Turner, Michael L.; Navarro, Oscar
Room temperature, solventless telomerization of isoprene with alcohols using (N-heterocyclic carbene)‒palladium catalysts
Catal. Sci. Technol., 2015, 5, 1447
1518675 CIFC27 H39 Cl2 N3 PdC 1 2/c 135.0018; 11.2158; 15.2054
90; 111.789; 90		5542.8Maluenda, Irene; Chen, Ming-Tsz; Guest, Daniel; Mark Roe, S.; Turner, Michael L.; Navarro, Oscar
Room temperature, solventless telomerization of isoprene with alcohols using (N-heterocyclic carbene)‒palladium catalysts
Catal. Sci. Technol., 2015, 5, 1447
1518676 CIFC17 H25 N O2 SiP 1 21/n 17.8451; 10.8055; 41.681
90; 92.188; 90		3530.7Wu, Shangze; Zeng, Rong; Fu, Chunling; Yu, Yihua; Zhang, Xue; Ma, Shengming
Rhodium-catalyzed C‒H functionalization-based approach to eight-membered lactams
Chem. Sci., 2015, 6, 2275
1518677 CIFC19 H19 Cl2 N O SP 1 21/c 19.4678; 22.465; 8.4857
90; 94.892; 90		1798.3Wu, Shangze; Zeng, Rong; Fu, Chunling; Yu, Yihua; Zhang, Xue; Ma, Shengming
Rhodium-catalyzed C–H functionalization-based approach to eight-membered lactams
Chem. Sci., 2015, 6, 2275
1518678 CIFC254 H317 Cd18 Cl8 Eu6 N18 O92P -351.305; 51.305; 24.419
90; 90; 120		55664Jones, Richard A.; Gnanam, Annie J.; Arambula, Jonathan F.; Jones, Jessica N.; Swaminathan, Jagannath; Yang, Xiaoping; Schipper, Desmond; Hall, Justin W.; DePue, Lauren J.; Dieye, Yakhya; Vadivelu, Jamuna; Chandler, Don J.; Marcotte, Edward M.; Sessler, Jonathan L.; Ehrlich, Lauren I. R.; Brown, Katherine A.
Lanthanide nano-drums: a new class of molecular nanoparticles for potential biomedical applications
Faraday Discuss., 2014
1518679 CIFC254 H317 Cd18 Cl8 N18 O92 Tb6P -351.114; 51.114; 24.362
90; 90; 120		55122Jones, Richard A.; Gnanam, Annie J.; Arambula, Jonathan F.; Jones, Jessica N.; Swaminathan, Jagannath; Yang, Xiaoping; Schipper, Desmond; Hall, Justin W.; DePue, Lauren J.; Dieye, Yakhya; Vadivelu, Jamuna; Chandler, Don J.; Marcotte, Edward M.; Sessler, Jonathan L.; Ehrlich, Lauren I. R.; Brown, Katherine A.
Lanthanide nano-drums: a new class of molecular nanoparticles for potential biomedical applications
Faraday Discuss., 2014
1518680 CIFC21 H31 Ni O3 P SP 1 21/n 19.5684; 16.352; 13.9609
90; 95.255; 90		2175.18Chen, Min; Zou, Wenping; Cai, Zhengguo; Chen, Changle
Norbornene homopolymerization and copolymerization with ethylene by phosphine-sulfonate nickel catalysts
Polym. Chem., 2015, 6, 2669
1518681 CIFC46 H39 B F15 Ni O3 P SP n a 2124.5629; 15.6599; 11.5597
90; 90; 90		4446.47Chen, Min; Zou, Wenping; Cai, Zhengguo; Chen, Changle
Norbornene homopolymerization and copolymerization with ethylene by phosphine-sulfonate nickel catalysts
Polym. Chem., 2015, 6, 2669
1518682 CIFH18 N8 Ni O6F m -3 m10.8738; 10.8738; 10.8738
90; 90; 90		1285.71Breternitz, Joachim; Farrugia, Louis J.; Godula-Jopek, Agata; Saremi-Yarahmadi, Sina; Malka, Iwona E.; Hoang, Tuan K.A.; Gregory, Duncan H.
Reaction of [Ni(H2O)6](NO3)2 with gaseous NH3; crystal growth via in-situ solvation
Journal of Crystal Growth, 2015, 412, 1
1518683 CIFH12 N2 Ni O12P -15.7531; 7.6604; 11.4876
106.347; 98.45; 101.538		464.73Breternitz, Joachim; Farrugia, Louis J.; Godula-Jopek, Agata; Saremi-Yarahmadi, Sina; Malka, Iwona E.; Hoang, Tuan K.A.; Gregory, Duncan H.
Reaction of [Ni(H2O)6](NO3)2 with gaseous NH3; crystal growth via in-situ solvation
Journal of Crystal Growth, 2015, 412, 1
1518684 CIFH12 N2 Ni O12P -15.8056; 7.7023; 11.6864
105.841; 98.451; 102.203		479.59Breternitz, Joachim; Farrugia, Louis J.; Godula-Jopek, Agata; Saremi-Yarahmadi, Sina; Malka, Iwona E.; Hoang, Tuan K.A.; Gregory, Duncan H.
Reaction of [Ni(H2O)6](NO3)2 with gaseous NH3; crystal growth via in-situ solvation
Journal of Crystal Growth, 2015, 412, 1
1518685 CIFC52 H48 N4 O4P n a 2118.809; 10.08; 20.725
90; 90; 90		3929Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu
Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.
Organic letters, 2015, 17, 786-789
1518686 CIFC62 H66 Cl6 N4 O12P -19.8315; 14.743; 21.249
101.193; 91.334; 94.028		3011.8Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu
Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.
Organic letters, 2015, 17, 786-789
1518687 CIFC63 H70 N4 O16P -111.12; 14.029; 20.02
108.726; 98.537; 94.981		2894.8Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu
Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior.
Organic letters, 2015, 17, 786-789
1518688 CIFC5 H6 N2 O2P 1 21/c 112.889; 6.852; 6.784
90; 104.92; 90		578.9Gustavo Portalone; Luigi Bencivenni; Marcello Colapietro; Andrea Pieretti; Fabio Ramondo
The effect of hydrogen bonding on the structures of uracil and some methyl derivatives studied by experiment and theory
Acta Chemica Scandinavica, 1999, 53, 57-68
1518689 CIFC32 H30 B2 N2 O5P 1 21/n 117.2259; 19.4533; 25.7366
90; 103.161; 90		8397.8Sumida, Yuto; Harada, Ryu; Kato-Sumida, Tomoe; Johmoto, Kohei; Uekusa, Hidehiro; Hosoya, Takamitsu
Boron-Selective Biaryl Coupling Approach to Versatile Dibenzoxaborins and Application to Concise Synthesis of Defucogilvocarcin M.
Organic letters, 2014, 16, 6240
1518690 CIFC18 H11 B O2P 1 21/c 15.1612; 15.5151; 15.9033
90; 91.214; 90		1273.2Sumida, Yuto; Harada, Ryu; Kato-Sumida, Tomoe; Johmoto, Kohei; Uekusa, Hidehiro; Hosoya, Takamitsu
Boron-Selective Biaryl Coupling Approach to Versatile Dibenzoxaborins and Application to Concise Synthesis of Defucogilvocarcin M.
Organic letters, 2014, 16, 6240
1518691 CIFC31 H27 N3 O3 SP -18.6968; 10.9553; 15.8049
72.6652; 85.8533; 80.1743		1415.98Chen, Hui; Kaga, Atsushi; Chiba, Shunsuke
Diastereoselective Aminooxygenation and Diamination of Alkenes with Amidines by Hypervalent Iodine(III) Reagents.
Organic letters, 2014, 16, 6136
1518692 CIFC24 H23 Cl3 N2 OP 1 21/n 18.8866; 11.3293; 21.9439
90; 93.332; 90		2205.55Chen, Hui; Kaga, Atsushi; Chiba, Shunsuke
Diastereoselective Aminooxygenation and Diamination of Alkenes with Amidines by Hypervalent Iodine(III) Reagents.
Organic letters, 2014, 16, 6136
1518693 CIFC23 H22 N2 OP 1 21 112.6259; 5.511; 13.3809
90; 107.086; 90		889.97Chen, Hui; Kaga, Atsushi; Chiba, Shunsuke
Diastereoselective Aminooxygenation and Diamination of Alkenes with Amidines by Hypervalent Iodine(III) Reagents.
Organic letters, 2014, 16, 6136
1518694 CIFC22 H20 N2C 1 2/c 131.6185; 5.5769; 18.4042
90; 93.168; 90		3240.3Chen, Hui; Kaga, Atsushi; Chiba, Shunsuke
Diastereoselective Aminooxygenation and Diamination of Alkenes with Amidines by Hypervalent Iodine(III) Reagents.
Organic letters, 2014, 16, 6136
1518695 CIFC36 H33 N3 O4 S2P 1 21/n 118.5262; 9.0722; 18.7024
90; 94.6251; 90		3133.1Chen, Hui; Kaga, Atsushi; Chiba, Shunsuke
Diastereoselective Aminooxygenation and Diamination of Alkenes with Amidines by Hypervalent Iodine(III) Reagents.
Organic letters, 2014, 16, 6136
1518696 CIFC23 H22 N2 OP 1 21/c 15.8261; 10.6516; 28.626
90; 95.011; 90		1769.7Chen, Hui; Kaga, Atsushi; Chiba, Shunsuke
Diastereoselective Aminooxygenation and Diamination of Alkenes with Amidines by Hypervalent Iodine(III) Reagents.
Organic letters, 2014, 16, 6136
1518697 CIFC22 H20 N2 OP 1 21 112.03; 5.6222; 13.018
90; 107.387; 90		840.2Chen, Hui; Kaga, Atsushi; Chiba, Shunsuke
Diastereoselective Aminooxygenation and Diamination of Alkenes with Amidines by Hypervalent Iodine(III) Reagents.
Organic letters, 2014, 16, 6136
1518698 CIFC22 H26 O3P 21 21 215.7161; 13.5777; 24.259
90; 90; 90		1882.78Fàbregas, Mireia; Gómez-Palomino, Alejandro; Pellicena, Miquel; Reina, Daniel F.; Romea, Pedro; Urpí, Fèlix; Font-Bardia, Mercè
Substrate-Controlled Michael Additions of Chiral Ketones to Enones.
Organic letters, 2014, 16, 6220
1518699 CIFC33 H29 F2 O5 PP 1 21/n 19.2855; 30.8566; 9.7988
90; 95.17; 90		2796.12Levin, Vitalij V.; Trifonov, Alexey L.; Zemtsov, Artem A.; Struchkova, Marina I.; Arkhipov, Dmitry E.; Dilman, Alexander D.
Difluoromethylene Phosphabetaine as an Equivalent of Difluoromethyl Carbanion.
Organic letters, 2014, 16, 6256
1518700 CIFC82 H88 N4 O12P -112.572; 14.553; 20.155
96.735; 103.439; 101.565		3461.4Kim, Sung Kuk; Lynch, Vincent M.; Sessler, Jonathan L.
Cone Calix[4]arene Diethyl Ester Strapped Calix[4]pyrrole: A Selective Receptor for the Fluoride Anion.
Organic letters, 2014, 16, 6128
1518701 CIFC80 H85 Cl3 Cs F N4 O11P 1 21/n 111.09; 33.038; 20.233
90; 102.967; 90		7224.2Kim, Sung Kuk; Lynch, Vincent M.; Sessler, Jonathan L.
Cone Calix[4]arene Diethyl Ester Strapped Calix[4]pyrrole: A Selective Receptor for the Fluoride Anion.
Organic letters, 2014, 16, 6128
1518702 CIFC79 H86 N4 O12P 1 21/c 116.8102; 21.0789; 19.1698
90; 94.179; 90		6774.6Kim, Sung Kuk; Lynch, Vincent M.; Sessler, Jonathan L.
Cone Calix[4]arene Diethyl Ester Strapped Calix[4]pyrrole: A Selective Receptor for the Fluoride Anion.
Organic letters, 2014, 16, 6128
1518703 CIFC144 H96 Cl4 F N14 O8I 1 2/a 119.9315; 23.719; 20.402
90; 116.015; 90		8667.9Kim, Sung Kuk; Lynch, Vincent M.; Sessler, Jonathan L.
Cone Calix[4]arene Diethyl Ester Strapped Calix[4]pyrrole: A Selective Receptor for the Fluoride Anion.
Organic letters, 2014, 16, 6128
1518704 CIFC19 H14 N2P 1 21/c 113.144; 8.737; 12.237
90; 92.09; 90		1404.4Pang, Xinlong; Chen, Chao; Su, Xiang; Li, Ming; Wen, Lirong
Diverse Tandem Cyclization Reactions of o-Cyanoanilines and Diaryliodonium Salts with Copper Catalyst for the Construction of Quinazolinimine and Acridine Scaffolds.
Organic letters, 2014, 16, 6228
1518705 CIFC23 H21 Br N4P 1 21/c 113.68; 17.357; 8.158
90; 97.15; 90		1922Pang, Xinlong; Chen, Chao; Su, Xiang; Li, Ming; Wen, Lirong
Diverse Tandem Cyclization Reactions of o-Cyanoanilines and Diaryliodonium Salts with Copper Catalyst for the Construction of Quinazolinimine and Acridine Scaffolds.
Organic letters, 2014, 16, 6228
1518706 CIFAl10 Cl2 H16 K12 O48 Si10I 2 2 29.88; 9.877; 13.064
90; 90; 90		1274.8Norlund Christensen, A.; Fjellvag, H.
Neutron powder diffraction study of the dehydration of zeolite N
Acta Chemica Scandinavica, 1999, 53, 85-89
1518707 CIFAl10 Cl2 H16 K12 O48 Si10I 2 2 29.779; 9.743; 13.142
90; 90; 90		1252.1Norlund Christensen, A.; Fjellvag, H.
Neutron powder diffraction study of the dehydration of zeolite N
Acta Chemica Scandinavica, 1999, 53, 85-89
1518708 CIFC56 H57 Cl3 La N15 O12P 21 21 2112.882; 21.1; 22.706
90; 90; 90		6172Liu Jiacheng; Song Zhigang; Wang Liufang; Zhuang Jinzhong; Huang Xiaoying
Preparation and characterization of lanthanides(III) complexes with polybenzimidazole ligands. Crystal structure of bis[tris(N-methyl-1-benzimidazol-2-yl)-amine]lanthanum(III) perchlorate monoacetonitrile solvate
Acta Chemica Scandinavica, 1999, 53, 90-94
1518709 CIFCa H21 N7 S6P 1 21/c 112.143; 11.815; 11.505
90; 93.53; 90		1647.5Schimek, George L.; Drake, Greg W.; Kolis, Joseph W.
Crystal Structure of Calcium Heptaammine Hexasulfide, Ca(NH3)7S6
Acta Chemica Scandinavica, 1999, 53, 145-148
1518710 CIFC18 H53 Cr2 N6 O16 S3P 1 21/n 18.42; 20.526; 18.877
90; 91.1; 90		3261.9Kalsbeek, Nicoline; Larsen, Sine
Crystal Structure of Tri-mu-hydroxobis[(1,4,7-trimethyl-1,4,7-triazacyclononane)chromium(III)] Dithionate Tetrahydrate
Acta Chemica Scandinavica, 1999, 53, 149-154
1518711 CIFC15 H22 O5P 1 21/c 113.3435; 7.2491; 15.3576
90; 92.261; 90		1484.36Peng, Jin-Bao; Qi, Yue; Jing, Ze-Ran; Wang, Shao-Hua; Tu, Yong-Qiang; Zhu, Dao-Yong; Zhang, Fu-Min
Efficient Oxa-Diels–Alder/Semipinacol Rearrangement/Aldol Cascade Reaction: Short Approach to Polycyclic Architectures
Organic Letters, 2015, 150209135056006
1518712 CIFC21 H28 O3P 21 21 216.0078; 15.1366; 20.0221
90; 90; 90		1820.76Parr, Brendan T.; Davies, Huw M. L.
Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence.
Organic letters, 2015, 17, 794-797
1518713 CIFC23 H27 F3 O3P 21 21 216.2097; 14.9142; 23.193
90; 90; 90		2147.97Parr, Brendan T.; Davies, Huw M. L.
Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence.
Organic letters, 2015, 17, 794-797
1518714 CIFC14 H26 Cl3 N4 O P RuP 1 21/n 16.9163; 23.66; 11.8396
90; 97.078; 90		1922.7Babak, Maria V.; Meier, Samuel M.; Huber, Kilian V. M.; Reynisson, Jóhannes; Legin, Anton A.; Jakupec, Michael A.; Roller, Alexander; Stukalov, Alexey; Gridling, Manuela; Bennett, Keiryn L.; Colinge, Jacques; Berger, Walter; Dyson, Paul J.; Superti-Furga, Giulio; Keppler, Bernhard K.; Hartinger, Christian G.
Target profiling of an antimetastatic RAPTA agent by chemical proteomics: relevance to the mode of action
Chem. Sci., 2015, 6, 2449
1518715 CIFC15 H23 Cl2 N4 O P RuP -110.5379; 12.8283; 13.7451
100.766; 97.279; 91.491		1808.34Babak, Maria V.; Meier, Samuel M.; Huber, Kilian V. M.; Reynisson, Jóhannes; Legin, Anton A.; Jakupec, Michael A.; Roller, Alexander; Stukalov, Alexey; Gridling, Manuela; Bennett, Keiryn L.; Colinge, Jacques; Berger, Walter; Dyson, Paul J.; Superti-Furga, Giulio; Keppler, Bernhard K.; Hartinger, Christian G.
Target profiling of an antimetastatic RAPTA agent by chemical proteomics: relevance to the mode of action
Chem. Sci., 2015, 6, 2449
1518716 CIFC42 H55 Cl2 N5 O10C 1 2 125.187; 8.1556; 21.154
90; 99.308; 90		4288.1Rose, Tristan E.; Lawson, Kenneth V.; Harran, Patrick. G.
Large ring-forming alkylations provide facile access to composite macrocycles
Chem. Sci., 2015, 6, 2219
1518717 CIFC18 H27 B Br N O5 SP -19.483; 13.115; 17.336
90.88; 99.38; 91.32		2126.3Carrillo, Josué Ayuso; Ingleson, Michael J.; Turner, Michael L.
Thienyl MIDA Boronate Esters as Highly Effective Monomers for Suzuki–Miyaura Polymerization Reactions
Macromolecules, 2015, 48, 979
1518718 CIFC18 H26 O4 SiP b c a16.759; 7.4334; 30.141
90; 90; 90		3754.9Xu, Xinfang; Wang, Xiangbo; Zavalij, Peter Y.; Doyle, Michael P.
Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade.
Organic letters, 2015, 17, 790-793
1518719 CIFC18 H26 O4 SiP -16.1239; 16.8945; 17.8873
91.468; 95.3024; 90.184		1842.1Xu, Xinfang; Wang, Xiangbo; Zavalij, Peter Y.; Doyle, Michael P.
Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade.
Organic letters, 2015, 17, 790-793

Blue left arrow Blue left arrow First | Blue left arrow Previous 300 | of 1758 | Next 300 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!
Top of the page
All data in the COD and the database itself are dedicated to the public domain and licensed under the CC0 License . Users of the data should acknowledge the original authors of the structural data.