Crystallography Open Database
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Searching year of publication is 2015
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1518411 | CIF | C42 H32 N2 O2 | P -1 | 11.1806; 11.4458; 12.861 101.527; 91.283; 99.274 | 1589.02 | Chen, Ming; Li, Lingzhi; Nie, Han; Tong, Jiaqi; Yan, Lulin; Xu, Bin; Sun, Jing Zhi; Tian, Wenjing; Zhao, Zujin; Qin, Anjun; Tang, Ben Zhong Tetraphenylpyrazine-based AIEgens: facile preparation and tunable light emission Chem. Sci., 2015, 6, 1932 |
| 1518412 | CIF | C32 H28 N2 O4 | P -1 | 9.768; 12.3063; 12.4687 68.542; 70.492; 88.089 | 1308.1 | Chen, Ming; Li, Lingzhi; Nie, Han; Tong, Jiaqi; Yan, Lulin; Xu, Bin; Sun, Jing Zhi; Tian, Wenjing; Zhao, Zujin; Qin, Anjun; Tang, Ben Zhong Tetraphenylpyrazine-based AIEgens: facile preparation and tunable light emission Chem. Sci., 2015, 6, 1932 |
| 1518413 | CIF | C41 H39 N7 O5 | P -1 | 10.244; 13.8307; 14.5665 72.3415; 70.128; 75.9246 | 1826.7 | Mahapatra, Ajit Kumar; Manna, Saikat Kumar; Maiti, Kalipada; Mondal, Sanchita; Maji, Rajkishor; Mandal, Debasish; Mandal, Sukhendu; Uddin, Md Raihan; Goswami, Shyamaprosad; Quah, Ching Kheng; Fun, Hoong-Kun An azodye-rhodamine-based fluorescent and colorimetric probe specific for the detection of Pd(2+) in aqueous ethanolic solution: synthesis, XRD characterization, computational studies and imaging in live cells. The Analyst, 2015, 140, 1229-1236 |
| 1518416 | CIF | C34 H35 N O14 | P 1 | 7.4957; 12.0298; 17.8347 87.387; 87.555; 74.708 | 1548.85 | Moon, 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 |
| 1518421 | CIF | C23 H28 N2 O4 S | P 1 21/n 1 | 10.543; 9.344; 22.465 90; 92.128; 90 | 2211.6 | Xu, 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 | CIF | C23 H28 N2 O4 S | P n a 21 | 26.688; 18.145; 9.062 90; 90; 90 | 4388.3 | Xu, 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 |
| 1518427 | CIF | C15 H9 F3 N2 O2 | P 1 21/n 1 | 16.6085; 7.853; 20.7239 90; 103.721; 90 | 2625.8 | Kumar, 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 | CIF | C15 H11 Cl N2 O2 | C 1 2/c 1 | 19.16; 11.3942; 15.345 90; 126.612; 90 | 2689 | Kumar, 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 |
| 1518432 | CIF | C6 H12 O6 | P 21 21 21 | 10.336; 14.852; 4.924 90; 90; 90 | 755.9 | Patyk, Ewa; Katrusiak, Andrzej Transformable H-bonds and conformation in compressed glucose Chem. Sci., 2015, 6, 1991 |
| 1518433 | CIF | C6 H12 O6 | P 21 21 21 | 10.26; 14.837; 4.8169 90; 90; 90 | 733.3 | Patyk, Ewa; Katrusiak, Andrzej Transformable H-bonds and conformation in compressed glucose Chem. Sci., 2015, 6, 1991 |
| 1518434 | CIF | C6 H12 O6 | P 21 21 21 | 10.22; 14.832; 4.7689 90; 90; 90 | 722.9 | Patyk, Ewa; Katrusiak, Andrzej Transformable H-bonds and conformation in compressed glucose Chem. Sci., 2015, 6, 1991 |
| 1518435 | CIF | C6 H12 O6 | P 21 21 21 | 10.218; 14.823; 4.7439 90; 90; 90 | 718.5 | Patyk, Ewa; Katrusiak, Andrzej Transformable H-bonds and conformation in compressed glucose Chem. Sci., 2015, 6, 1991 |
| 1518436 | CIF | C6 H12 O6 | P 21 21 21 | 10.181; 14.808; 4.693 90; 90; 90 | 707.5 | Patyk, Ewa; Katrusiak, Andrzej Transformable H-bonds and conformation in compressed glucose Chem. Sci., 2015, 6, 1991 |
| 1518437 | CIF | C6 H12 O6 | P 21 21 21 | 10.11; 14.808; 4.5801 90; 90; 90 | 685.7 | Patyk, Ewa; Katrusiak, Andrzej Transformable H-bonds and conformation in compressed glucose Chem. Sci., 2015, 6, 1991 |
| 1518438 | CIF | C6 H12 O6 | P 21 21 21 | 10.06; 14.798; 4.537 90; 90; 90 | 675.4 | Patyk, Ewa; Katrusiak, Andrzej Transformable H-bonds and conformation in compressed glucose Chem. Sci., 2015, 6, 1991 |
| 1518439 | CIF | C6 H12 O6 | P 21 21 21 | 10.05; 14.807; 4.4206 90; 90; 90 | 657.8 | Patyk, Ewa; Katrusiak, Andrzej Transformable H-bonds and conformation in compressed glucose Chem. Sci., 2015, 6, 1991 |
| 1518440 | CIF | C6 H12 O6 | P 21 21 21 | 10.04; 14.796; 4.3879 90; 90; 90 | 651.8 | Patyk, Ewa; Katrusiak, Andrzej Transformable H-bonds and conformation in compressed glucose Chem. Sci., 2015, 6, 1991 |
| 1518441 | CIF | C6 H12 O6 | P 21 21 21 | 10.056; 14.779; 4.275 90; 90; 90 | 635.3 | Patyk, Ewa; Katrusiak, Andrzej Transformable H-bonds and conformation in compressed glucose Chem. Sci., 2015, 6, 1991 |
| 1518442 | CIF | C6 H12 O6 | P 21 21 21 | 10.059; 14.776; 4.261 90; 90; 90 | 633.3 | Patyk, Ewa; Katrusiak, Andrzej Transformable H-bonds and conformation in compressed glucose Chem. Sci., 2015, 6, 1991 |
| 1518443 | CIF | C6 H12 O6 | P 21 21 21 | 10.063; 14.787; 4.256 90; 90; 90 | 633.3 | Patyk, Ewa; Katrusiak, Andrzej Transformable H-bonds and conformation in compressed glucose Chem. Sci., 2015, 6, 1991 |
| 1518444 | CIF | C6 H12 O6 | P 21 21 21 | 9.714; 14.99; 4.262 90; 90; 90 | 621 | Patyk, Ewa; Katrusiak, Andrzej Transformable H-bonds and conformation in compressed glucose Chem. Sci., 2015, 6, 1991 |
| 1518445 | CIF | C6 H12 O6 | P 21 21 21 | 9.73; 14.987; 4.234 90; 90; 90 | 617.4 | Patyk, Ewa; Katrusiak, Andrzej Transformable H-bonds and conformation in compressed glucose Chem. Sci., 2015, 6, 1991 |
| 1518446 | CIF | C6 H12 O6 | P 21 21 21 | 9.694; 14.931; 4.2234 90; 90; 90 | 611.3 | Patyk, Ewa; Katrusiak, Andrzej Transformable H-bonds and conformation in compressed glucose Chem. Sci., 2015, 6, 1991 |
| 1518447 | CIF | C67 F6 | P b c a | 9.9998; 20.6538; 31.3512 90; 90; 90 | 6475.1 | San, 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 | CIF | C60 H60 Li4 O5 Rb4 | C m c m | 14.166; 13.519; 25.901 90; 90; 90 | 4960 | Filatov, 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 | CIF | C66 H80 Li3 O12.5 Rb5 | P -1 | 10.064; 15.27; 22.129 90.416; 93.102; 94.532 | 3384.9 | Filatov, 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 | CIF | C28 H46 N4 O19 Tm | C 1 c 1 | 23.1686; 9.677; 16.8001 90; 118.272; 90 | 3317.3 | Funk, 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 | CIF | C33 H31.75 N2 O5.88 | C 1 2 1 | 52.27; 5.01; 22.83 90; 105.49; 90 | 5761 | Raeburn, 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 | CIF | C36 H58 Cl N3 O2 | P 32 | 15.865; 15.865; 11.7214 90; 90; 120 | 2555 | Bandar, 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 | CIF | C32 H31 F3 N4 O6 | I 41/a | 28.1062; 28.1062; 14.709 90; 90; 90 | 11619.5 | Jiao, 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 | CIF | C11 H18 N8 O3 | P m n 21 | 9.5289; 9.1191; 8.667 90; 90; 90 | 753.12 | Gryl, 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 | CIF | C29 H37 N3 O4 | P 21 21 21 | 7.788; 16.0615; 20.7023 90; 90; 90 | 2589.6 | Lee, Pin-Sheng; Yoshikai, Naohiko Cobalt-catalyzed enantioselective directed C-h alkylation of indole with styrenes. Organic letters, 2015, 17, 22-25 |
| 1518456 | CIF | C21 H28 O4 S | C 1 2 1 | 19.3925; 6.0017; 17.9993 90; 107.635; 90 | 1996.45 | Lan, 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 | CIF | C21 H28 O4 | P 21 21 21 | 6.2688; 16.308; 18.2849 90; 90; 90 | 1869.29 | Lan, 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 | CIF | C24 H25 N O5 | P 21 21 21 | 9.0419; 12.2803; 19.0748 90; 90; 90 | 2118.01 | Liu, 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 | CIF | C24 H23 N O4 | P 1 21/c 1 | 9.6257; 24.6776; 9.1983 90; 108.936; 90 | 2066.71 | Liu, 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 | CIF | C25 H25 N O4 | P -1 | 10.1067; 11.5787; 19.2079 83.811; 82.159; 76.354 | 2157.2 | Liu, 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 | CIF | C24 H21 Cl2 N O4 | C 1 2 1 | 21.3083; 16.6395; 17.8923 90; 118.967; 90 | 5550.3 | Liu, 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 | CIF | C21 H21 Br N2 O3 S | P c a 21 | 24.0183; 11.2598; 7.4174 90; 90; 90 | 2005.97 | Arai, 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 | CIF | C21 H21 Br N2 O3 S | P 1 21/n 1 | 8.12; 11.101; 21.7055 90; 94.955; 90 | 1949.2 | Arai, 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 | CIF | C19 H26 O7 | P 21 21 21 | 9.1452; 12.5627; 16.2841 90; 90; 90 | 1870.85 | Xu, 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 | CIF | C19 H26 O7 | P 32 | 9.2683; 9.2683; 18.5901 90; 90; 120 | 1382.97 | Xu, 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 | CIF | C24.5 H26.52 O7 | C 1 2 1 | 43.491; 5.5109; 18.3225 90; 95.331; 90 | 4372.4 | McDonald, 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 | CIF | C18 H26 O4 | P -1 | 7.1391; 7.5445; 15.455 88.709; 83.268; 76.661 | 804.4 | Suizu, Hiroshi; Shigeoka, Daisuke; Aoyama, Hiroshi; Yoshimitsu, Takehiko Total synthesis of clavilactone B: a radical cyclization-fragmentation strategy. Organic letters, 2015, 17, 126-129 |
| 1518468 | CIF | C19 H24 O7 S | P 1 21/n 1 | 16.194; 6.597; 18.175 90; 102.603; 90 | 1894.9 | Suizu, Hiroshi; Shigeoka, Daisuke; Aoyama, Hiroshi; Yoshimitsu, Takehiko Total synthesis of clavilactone B: a radical cyclization-fragmentation strategy. Organic letters, 2015, 17, 126-129 |
| 1518469 | CIF | C21 H10 Au B Cl10 N6 Pb | P -1 | 8.5794; 13.7444; 13.7913 110.805; 93.371; 101.13 | 1477.17 | Echeverría, 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 | CIF | C18 H21 N3 O13 | P 1 21/c 1 | 10.0519; 11.0764; 19.917 90; 115.105; 90 | 2008 | Ivanova, B.; Spiteller, M. Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil Environmental Geochemistry and Health, 2015 |
| 1518471 | CIF | C8 H15 N2 O3 | P 1 21/n 1 | 8.504; 11.8666; 9.5595 90; 96.868; 90 | 957.8 | Ivanova, B.; Spiteller, M. Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil Environmental Geochemistry and Health, 2015 |
| 1518472 | CIF | C9 H17 N2 O2 | P 1 21/c 1 | 10.928; 6.85; 14.18 90; 91.265; 90 | 1061.2 | Ivanova, B.; Spiteller, M. Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil Environmental Geochemistry and Health, 2015 |
| 1518473 | CIF | C28 H27 N4 O16 | C 1 2/c 1 | 17.65; 7.5376; 22.793 90; 91.608; 90 | 3031.2 | Ivanova, B.; Spiteller, M. Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil Environmental Geochemistry and Health, 2015 |
| 1518474 | CIF | C8 H15 N2 O3 | P 1 21/c 1 | 10.028; 9.435; 11.76 90; 122.95; 90 | 934 | Ivanova, B.; Spiteller, M. Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil Environmental Geochemistry and Health, 2015 |
| 1518475 | CIF | C19 H22 N2 O13 | P 1 21/n 1 | 9.975; 11.085; 18.066 90; 94.823; 90 | 1990.5 | Ivanova, B.; Spiteller, M. Solid-state UV-MALDI mass spectrometric quantitation of fluroxypyr and triclopyr in soil Environmental Geochemistry and Health, 2015 |
| 1518476 | CIF | C14 H23 F6 O6 Pd Sb | P -1 | 9.539; 10.408; 11.253 115.767; 97.422; 91.945 | 992.6 | Commarieu, 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 | CIF | C15 H22 F6 N O6 Pd Sb | P n m a | 18.89; 16.805; 13.196 90; 90; 90 | 4189 | Commarieu, 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 | CIF | C22 H35 F6 O6 Pd Sb | P n a 21 | 16.758; 16.947; 9.5046 90; 90; 90 | 2699.3 | Commarieu, 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 | CIF | C17 H28 F6 N3 O10 Pd Sb | P 1 21/c 1 | 10.0271; 19.0026; 14.5138 90; 92.747; 90 | 2762.3 | Commarieu, 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 | CIF | C66 H86 Cl20 F24 O16 Pd4 Sb4 | P -1 | 16.4284; 19.3745; 21.4447 66.181; 88.434; 72.775 | 5930.9 | Commarieu, 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 | CIF | C12 H15 Cl O6 | P 1 21 1 | 4.6451; 11.3065; 12.3885 90; 94.458; 90 | 648.67 | Wu, 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 | CIF | C24 H20 N2 O | P b c a | 8.8127; 13.2298; 32.5 90; 90; 90 | 3789.2 | Fan, 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 | CIF | C23 H24 Cl N O4 | P -1 | 10.0098; 10.1777; 12.0505 67.347; 70.617; 79.738 | 1066.95 | Craig, 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 | CIF | C54 H75 N8 O16 S | P 1 | 9.1948; 12.5947; 13.668 79.379; 77.83; 78.547 | 1499.6 | Ganesh 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 | CIF | C22 H16 I N O2 S | P 1 21/c 1 | 8.0428; 19.587; 12.8121 90; 104.921; 90 | 1950.29 | Sun, 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 | CIF | C21 H14 I N O2 S | P -1 | 8.195; 10.1773; 11.9407 86.942; 83.912; 76.661 | 963.13 | Sun, 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 | CIF | C24 H24 O6 | C 1 c 1 | 17.142; 9.0363; 12.653 90; 90.03; 90 | 1960 | Zhang, 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 | CIF | C16 H16 O5 | P n a 21 | 14.969; 7.307; 12.761 90; 90; 90 | 1395.8 | Zhang, 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 | CIF | C22 H14 Co2 O11 | P -1 | 8.0572; 8.3258; 17.63 88.79; 84.64; 75.45 | 1139.7 | Zhang, 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 | CIF | C36 H34 Co2 F6 N O5 P2 | P 21 21 2 | 15.8829; 19.5684; 11.5831 90; 90; 90 | 3600.1 | Orgué, 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 | CIF | C30 H37 Co2 N3 O5 P2 Si | P 1 21 1 | 8.8649; 20.8055; 9.1083 90; 101.487; 90 | 1646.3 | Orgué, 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 | CIF | C32 H22 B Cl3 F4 N2 O2 | C 1 2/c 1 | 30.8526; 11.997; 18.7562 90; 113.744; 90 | 6354.75 | Greulich, 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 | CIF | C15 H10 Cl N O3 | P 1 21/n 1 | 8.5347; 14.9824; 10.2813 90; 96.632; 90 | 1305.88 | Greulich, 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 | CIF | C18 H20 N2 O2 S | P c a 21 | 12.7796; 13.8018; 18.4448 90; 90; 90 | 3253.32 | Greulich, 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 | CIF | C16 H12 Br N3 | P 32 | 10.18; 10.18; 10.954 90; 90; 120 | 983.1 | Tang, 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 | CIF | C34 H58 As4 Co2 | P 1 21/n 1 | 8.4386; 13.7676; 16.0276 90; 100.27; 90 | 1832.24 | Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M. Synthesis of arsenic-rich Asnligand complexes from yellow arsenic Chem. Sci., 2015, 6, 1379 |
| 1518497 | CIF | C35 H60 As4 Cl2 Co2 | C 1 2/c 1 | 17.893; 19.9249; 11.6299 90; 107.903; 90 | 3945.5 | Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M. Synthesis of arsenic-rich Asnligand complexes from yellow arsenic Chem. Sci., 2015, 6, 1379 |
| 1518498 | CIF | C68 H116 As10 Co4 | P -1 | 10.3921; 14.3707; 14.8262 62.53; 76.535; 79.819 | 1904.35 | Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M. Synthesis of arsenic-rich Asnligand complexes from yellow arsenic Chem. Sci., 2015, 6, 1379 |
| 1518499 | CIF | C72 H124 As10 Cl8 Co4 | P -1 | 13.7956; 14.0892; 15.0382 62.971; 69.895; 61.292 | 2254 | Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M. Synthesis of arsenic-rich Asnligand complexes from yellow arsenic Chem. Sci., 2015, 6, 1379 |
| 1518500 | CIF | C51 H87 As12 Co3 | C 1 2/c 1 | 28.9202; 15.7899; 29.9375 90; 112.752; 90 | 12607.1 | Graßl, C.; Bodensteiner, M.; Zabel, M.; Scheer, M. Synthesis of arsenic-rich Asnligand complexes from yellow arsenic Chem. Sci., 2015, 6, 1379 |
| 1518501 | CIF | C23 H32 N2 Se | P n a 21 | 23.3; 7.0807; 11.6415 90; 90; 90 | 1920.6 | Vummaleti, 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 | CIF | C15 H24 N2 Se | P 1 21/c 1 | 11.8147; 11.1443; 12.2088 90; 108.21; 90 | 1527 | Vummaleti, 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 | CIF | C27 H48 N2 Se | P 1 21/n 1 | 14.4058; 7.4133; 25.023 90; 97.856; 90 | 2647.2 | Vummaleti, 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 | CIF | C19 H20 N2 Se | P 1 2/n 1 | 8.3318; 7.4265; 13.6459 90; 98.798; 90 | 834.42 | Vummaleti, 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 | CIF | C21 H24 N2 Se | P b c n | 16.043; 7.3937; 16.055 90; 90; 90 | 1904.4 | Vummaleti, 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 | CIF | C35 H52 N2 Se | P 1 21/c 1 | 20.433; 7.6327; 21.563 90; 106.66; 90 | 3221.8 | Vummaleti, 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 | CIF | C27 H34 Cl2 N2 Se | I 1 2/a 1 | 17.366; 9.4565; 21.295 90; 109.08; 90 | 3305 | Vummaleti, 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 | CIF | C21 H26 N2 Se | P b c n | 15.9194; 7.4418; 16.1915 90; 90; 90 | 1918.2 | Vummaleti, 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 | CIF | C11 H6 F5 N3 Se | P 1 21/c 1 | 9.3746; 15.527; 8.3524 90; 90.357; 90 | 1215.7 | Vummaleti, 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 | CIF | C11 H11 N3 O Se | P -1 | 7.8283; 7.9731; 18.447 97.93; 94.637; 90.042 | 1136.6 | Vummaleti, 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 | CIF | C21 H21 N3 O Se | P -1 | 8.5326; 10.637; 11.589 107.558; 101.546; 107.498 | 906.2 | Vummaleti, 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 | CIF | C30 H35 N3 O Se Si | P b c a | 13.2692; 19.8926; 20.979 90; 90; 90 | 5537.6 | Vummaleti, 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 |
| 1518526 | CIF | C12 H11 N O2 | P -1 | 4.00444; 11.1381; 12.202 71.955; 89.514; 80.992 | 510.62 | Surampudi, 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 | CIF | C38 H48 N2 O4 | P 1 21/c 1 | 14.93217; 14.22602; 15.93712 90; 100.89; 90 | 3324.49 | Surampudi, 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 | CIF | C30 H40 N2 O4 Si4 | P -1 | 8.5558; 11.887; 17.0071 99.115; 92.129; 94.397 | 1700.67 | Surampudi, 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 | CIF | C34 H52 N2 O4 Si6 | P -1 | 8.6514; 11.8373; 20.4256 82.751; 87.339; 86.175 | 2068.9 | Surampudi, 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 | CIF | C152.05 H75.74 Cl2.21 F40 N12 S8 | P -1 | 18.9073; 20.7452; 21.091 67.38; 77.21; 65.257 | 6917.2 | Mori, 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 | CIF | C87.05 H40.13 Cl3.96 F20 N6 S6 | C 1 2/c 1 | 49.998; 12.402; 35.242 90; 131.613; 90 | 16338 | Mori, 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 | CIF | C95.3 H48 Cl2.3 F20 N6 O0.5 S8 | P -1 | 17.2734; 18.9028; 30.1289 105; 92.92; 107.23 | 8989 | Mori, 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 | CIF | C90 H72 Ag12 F18 N6 O12 S6 | R -3 :H | 23.9571; 23.9571; 16.5415 90; 90; 120 | 8221.9 | Xu, 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 | CIF | C6 H4 F9 N3 O3 S | P 1 21/n 1 | 5.2742; 8.2719; 29.673 90; 93.124; 90 | 1292.64 | Luo, 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 | CIF | C6 H4 F9 N3 O3 S | P 1 21/n 1 | 5.351; 8.2492; 30.2383 90; 93.95; 90 | 1331.59 | Luo, 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 | CIF | C18 H11 F6 N O3 | C 1 2/c 1 | 32.403; 6.8959; 15.25 90; 97.03; 90 | 3382 | Lu, 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 |
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