Crystallography Open Database
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Searching year of publication is 2009
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1504272 | CIF | C73 H98 Cl2 N O7 P | P 21 21 21 | 13.662; 20.5772; 24.4019 90; 90; 90 | 6860 | Herbert, Simon A.; Arnott, Gareth E. An asymmetric ortholithiation approach to inherently chiral calix[4]arenes. Organic letters, 2009, 11, 4986-4989 |
| 1504273 | CIF | C57 H56 Cl2 N10 O5 | P 1 21/c 1 | 12.432; 21.192; 19.724 90; 106.37; 90 | 4986 | Xue, Min; Chen, Chuan-Feng Triptycene-derived N(H)-bridged azacalixarenes: synthesis, structure, and encapsulation of small neutral molecules in the solid state. Organic letters, 2009, 11, 5294-5297 |
| 1504274 | CIF | C10 H10 Cl2 N10 O | C 1 2/c 1 | 26.903; 19.366; 27.68 90; 112.55; 90 | 13319 | Xue, Min; Chen, Chuan-Feng Triptycene-derived N(H)-bridged azacalixarenes: synthesis, structure, and encapsulation of small neutral molecules in the solid state. Organic letters, 2009, 11, 5294-5297 |
| 1504275 | CIF | C59.27 H41.16 Cl3.61 N8 O9.57 | C 1 2/c 1 | 24.262; 27.241; 16.704 90; 102.147; 90 | 10793 | Xue, Min; Chen, Chuan-Feng Triptycene-derived N(H)-bridged azacalixarenes: synthesis, structure, and encapsulation of small neutral molecules in the solid state. Organic letters, 2009, 11, 5294-5297 |
| 1504276 | CIF | C50 H38 Cl2 N10 O5 | P -1 | 15.098; 15.275; 15.443 67.68; 61.26; 75.64 | 2879.4 | Xue, Min; Chen, Chuan-Feng Triptycene-derived N(H)-bridged azacalixarenes: synthesis, structure, and encapsulation of small neutral molecules in the solid state. Organic letters, 2009, 11, 5294-5297 |
| 1504277 | CIF | C15 H16 I N O3 | P 21 21 21 | 4.9426; 12.8163; 23.5105 90; 90; 90 | 1489.29 | Pal, Ujjwal; Ranatunga, Sujeewa; Ariyarathna, Yamuna; Del Valle, Juan R. Total synthesis of the putative structure of lucentamycin A. Organic letters, 2009, 11, 5298-5301 |
| 1504278 | CIF | C23 H41 Cl N2 O5 | P 32 | 13.3942; 13.3942; 27.3937 90; 90; 120 | 4256.1 | Pal, Ujjwal; Ranatunga, Sujeewa; Ariyarathna, Yamuna; Del Valle, Juan R. Total synthesis of the putative structure of lucentamycin A. Organic letters, 2009, 11, 5298-5301 |
| 1504279 | CIF | C15 H20 O2 | P 32 2 1 | 7.68; 7.68; 37.274 90; 90; 120 | 1904 | Magauer, Thomas; Mulzer, Johann; Tiefenbacher, Konrad Total syntheses of (+)-echinopine A and B: determination of absolute stereochemistry. Organic letters, 2009, 11, 5306-5309 |
| 1504280 | CIF | C18 H20 N8 O2 S2 | P n a 21 | 13.075; 16.85; 9.3 90; 90; 90 | 2049 | Avasthi, Kamlakar; Ansari, Amantullah; Tewari, Ashish K.; Kant, Ruchir; Maulik, Prakas R. Pyrazolo[3,4-d]pyrimidinophanes: convenient synthesis of a new class of cyclophane and X-ray structure of the first representative. Organic letters, 2009, 11, 5290-5293 |
| 1504281 | CIF | C60 H44 Br4 Cl6 N2 O4 | P 1 21/a 1 | 18.099; 8.285; 19.042 90; 105.218; 90 | 2755.2 | Nakazono, Satomi; Easwaramoorthi, Shanmugam; Kim, Dongho; Shinokubo, Hiroshi; Osuka, Atsuhiro Synthesis of arylated perylene bisimides through C-H bond cleavage under ruthenium catalysis. Organic letters, 2009, 11, 5426-5429 |
| 1504282 | CIF | C66 H48 F12 N4 O4 | P 1 21/c 1 | 18.3251; 8.2876; 18.7323 90; 103.654; 90 | 2764.5 | Nakazono, Satomi; Easwaramoorthi, Shanmugam; Kim, Dongho; Shinokubo, Hiroshi; Osuka, Atsuhiro Synthesis of arylated perylene bisimides through C-H bond cleavage under ruthenium catalysis. Organic letters, 2009, 11, 5426-5429 |
| 1504283 | CIF | C34 H34.36 Cl2.64 N3 O2 | P -1 | 9.294; 10.196; 18.474 85.694; 83.861; 66.29 | 1592.7 | Nakazono, Satomi; Easwaramoorthi, Shanmugam; Kim, Dongho; Shinokubo, Hiroshi; Osuka, Atsuhiro Synthesis of arylated perylene bisimides through C-H bond cleavage under ruthenium catalysis. Organic letters, 2009, 11, 5426-5429 |
| 1504284 | CIF | C76 H86 F12 N6 O18 S4 | P -1 | 6.815; 14.674; 20.572 70.543; 80.424; 84.6 | 1911 | Nakazono, Satomi; Easwaramoorthi, Shanmugam; Kim, Dongho; Shinokubo, Hiroshi; Osuka, Atsuhiro Synthesis of arylated perylene bisimides through C-H bond cleavage under ruthenium catalysis. Organic letters, 2009, 11, 5426-5429 |
| 1504285 | CIF | C87 H112 N6 O4 Zn | P 1 21/c 1 | 16.5956; 34.837; 14.5206 90; 115.729; 90 | 7562.7 | Maeda, Chihiro; Shinokubo, Hiroshi; Osuka, Atsuhiro meso,meso'-Bis(5-azaindol-2-yl)-appended meso-meso-linked Zn(II) diporphyrin: a discrete fluorescent assembly. Organic letters, 2009, 11, 5322-5325 |
| 1504286 | CIF | C16 H20 O6 | P 21 21 21 | 9.3413; 10.0343; 16.9972 90; 90; 90 | 1593.21 | Gharpure, Santosh J.; Shukla, Manoj K.; Vijayasree, U. Stereoselective synthesis of donor-acceptor substituted cyclopropafuranones by intramolecular cyclopropanation of vinylogous carbonates: divergent synthesis of tetrahydrofuran-3-one, tetrahydropyran-3-one, and lactones. Organic letters, 2009, 11, 5466-5469 |
| 1504287 | CIF | C7 H8 O4 | P 21 21 21 | 6.1758; 9.0571; 12.9827 90; 90; 90 | 726.19 | Gharpure, Santosh J.; Shukla, Manoj K.; Vijayasree, U. Stereoselective synthesis of donor-acceptor substituted cyclopropafuranones by intramolecular cyclopropanation of vinylogous carbonates: divergent synthesis of tetrahydrofuran-3-one, tetrahydropyran-3-one, and lactones. Organic letters, 2009, 11, 5466-5469 |
| 1504288 | CIF | C15 H16 O4 | P 1 21 1 | 5.0129; 8.5049; 15.8364 90; 93.115; 90 | 674.17 | Gharpure, Santosh J.; Shukla, Manoj K.; Vijayasree, U. Stereoselective synthesis of donor-acceptor substituted cyclopropafuranones by intramolecular cyclopropanation of vinylogous carbonates: divergent synthesis of tetrahydrofuran-3-one, tetrahydropyran-3-one, and lactones. Organic letters, 2009, 11, 5466-5469 |
| 1504289 | CIF | C18 H16 O3 | P -1 | 8.7638; 8.8421; 10.0304 74.58; 86.829; 67.601 | 691.83 | Lee, Doris; Newman, Stephen G.; Taylor, Mark S. Boron-catalyzed direct aldol reactions of pyruvic acids. Organic letters, 2009, 11, 5486-5489 |
| 1504290 | CIF | C28 H32 N2 O3 | P b c a | 12.587; 12.897; 30.669 90; 90; 90 | 4979 | Shintani, Ryo; Murakami, Masataka; Tsuji, Takaoki; Tanno, Hideyuki; Hayashi, Tamio Palladium-catalyzed decarboxylative [4 + 3] cyclization of gamma-methylidene-delta-valerolactones with 1,1-dicyanocyclopropanes. Organic letters, 2009, 11, 5642-5645 |
| 1504291 | CIF | C24 H22 N2 O2 | P -1 | 8.132; 9.139; 13.34 95.4; 90.65; 91.62 | 987 | Shintani, Ryo; Murakami, Masataka; Tsuji, Takaoki; Tanno, Hideyuki; Hayashi, Tamio Palladium-catalyzed decarboxylative [4 + 3] cyclization of gamma-methylidene-delta-valerolactones with 1,1-dicyanocyclopropanes. Organic letters, 2009, 11, 5642-5645 |
| 1504292 | CIF | C22 H25 N O4 S | P 21 21 2 | 36.79; 10.2861; 10.833 90; 90; 90 | 4099.5 | Shintani, Ryo; Murakami, Masataka; Tsuji, Takaoki; Tanno, Hideyuki; Hayashi, Tamio Palladium-catalyzed decarboxylative [4 + 3] cyclization of gamma-methylidene-delta-valerolactones with 1,1-dicyanocyclopropanes. Organic letters, 2009, 11, 5642-5645 |
| 1504293 | CIF | C11 H20 O2 | P -1 | 8.6882; 14.998; 15.059 117.59; 93.7; 98.17 | 1702.4 | Jones, Ian L.; Moore, Felicity K.; Chai, Christina L. L. Total synthesis of (+/-)-cordypyridones A and B and related epimers. Organic letters, 2009, 11, 5526-5529 |
| 1504294 | CIF | C18 H14 Cl N O | P 21 21 21 | 7.621; 8.393; 22.728 90; 90; 90 | 1453.8 | He, Wei; Yip, Kai-Tai; Zhu, Nian-Yong; Yang, Dan Pd(II)/(t)Bu-quinolineoxazoline: an air-stable and modular chiral catalyst system for enantioselective oxidative cascade cyclization. Organic letters, 2009, 11, 5626-5628 |
| 1504295 | CIF | C16.5 H19 Cl3 N2 O Pd | P 1 21 1 | 9.712; 20.705; 9.816 90; 108.77; 90 | 1868.9 | He, Wei; Yip, Kai-Tai; Zhu, Nian-Yong; Yang, Dan Pd(II)/(t)Bu-quinolineoxazoline: an air-stable and modular chiral catalyst system for enantioselective oxidative cascade cyclization. Organic letters, 2009, 11, 5626-5628 |
| 1504296 | CIF | C20 H29 N O3 | P 1 21 1 | 6.872; 9.187; 15.595 90; 97.384; 90 | 976.4 | Wang, Xia-Chang; Zheng, Zong-Ping; Gan, Xian-Wen; Hu, Li-Hong Jatrophalactam, a novel diterpenoid lactam isolated from Jatropha curcas. Organic letters, 2009, 11, 5522-5524 |
| 1504297 | CIF | C16 H11 N3 O3 | C 1 2/c 1 | 21.754; 8.501; 14.483 90; 102.299; 90 | 2616.9 | Yi, Chenyi; Liu, Shi-Xia; Neels, Antonia; Renaud, Philippe; Decurtins, Silvio Preparation of zwitterionic hydroquinone-fused [1,4]oxazinium derivatives via a photoinduced intramolecular dehydrogenative-coupling reaction. Organic letters, 2009, 11, 5530-5533 |
| 1504298 | CIF | C14 H12 N4 O4 | P -1 | 8.0209; 8.5834; 10.689 94.192; 104.4; 104.893 | 681.4 | Yi, Chenyi; Liu, Shi-Xia; Neels, Antonia; Renaud, Philippe; Decurtins, Silvio Preparation of zwitterionic hydroquinone-fused [1,4]oxazinium derivatives via a photoinduced intramolecular dehydrogenative-coupling reaction. Organic letters, 2009, 11, 5530-5533 |
| 1504299 | CIF | C10 H7 Br N4 O2 | P n a 21 | 10.595; 7.426; 13.938 90; 90; 90 | 1096.6 | Patriciu, Oana-Irina; Fînaru, Adriana-Luminita; Massip, Stéphane; Leger, Jean-Michel; Jarry, Christian; Guillaumet, Gérald Smiles rearrangement as a tool for the preparation of dihydrodipyridopyrazines. Organic letters, 2009, 11, 5502-5505 |
| 1504300 | CIF | C10 H9 Br N4 | P 1 21/n 1 | 8.638; 6.38; 18.833 90; 94.2; 90 | 1035.1 | Patriciu, Oana-Irina; Fînaru, Adriana-Luminita; Massip, Stéphane; Leger, Jean-Michel; Jarry, Christian; Guillaumet, Gérald Smiles rearrangement as a tool for the preparation of dihydrodipyridopyrazines. Organic letters, 2009, 11, 5502-5505 |
| 1504301 | CIF | C16 H19 Br N4 O | P -1 | 7.538; 10.542; 12.044 98.908; 102.359; 109.915 | 851.5 | Patriciu, Oana-Irina; Fînaru, Adriana-Luminita; Massip, Stéphane; Leger, Jean-Michel; Jarry, Christian; Guillaumet, Gérald Smiles rearrangement as a tool for the preparation of dihydrodipyridopyrazines. Organic letters, 2009, 11, 5502-5505 |
| 1504302 | CIF | C32 H43 Br Cl3 N O Si | P 21 21 21 | 10.2195; 13.6892; 23.5232 90; 90; 90 | 3290.8 | Dunn, Travis B.; Ellis, J. Michael; Kofink, Christiane C.; Manning, James R.; Overman, Larry E. Asymmetric construction of rings A-D of daphnicyclidin-type alkaloids. Organic letters, 2009, 11, 5658-5661 |
| 1504303 | CIF | C28 H24 N4 O4 S | P 1 21/n 1 | 9.0058; 13.1391; 21.485 90; 93.277; 90 | 2538.1 | Hong, Deng; Lin, Xufeng; Zhu, Yuanxun; Lei, Ming; Wang, Yanguang Copper-catalyzed tandem nucleophilic ring-opening/intramolecular oxidative amidation of N-tosylaziridines and hydrazones under aerobic conditions. Organic letters, 2009, 11, 5678-5681 |
| 1504304 | CIF | C16 H19 N O3 | P 21 21 21 | 6.2054; 10.304; 21.8082 90; 90; 90 | 1394.43 | Presset, Marc; Coquerel, Yoann; Rodriguez, Jean Microwave-assisted domino and multicomponent reactions with cyclic acylketenes: expeditious syntheses of oxazinones and oxazindiones. Organic letters, 2009, 11, 5706-5709 |
| 1504305 | CIF | C19 H21 N O6 | P 1 21 1 | 9.293; 8.065; 11.846 90; 92.98; 90 | 886.6 | McGarraugh, Patrick G.; Brenner, Stacey E. A new organocatalyzed Michael-Michael cascade reaction generates highly substituted fused carbocycles. Organic letters, 2009, 11, 5654-5657 |
| 1504306 | CIF | C30 H55 N O4 Si | P 21 21 21 | 9.5398; 10.677; 30.01 90; 90; 90 | 3056.7 | Nakayama, Atsushi; Kogure, Noriyuki; Kitajima, Mariko; Takayama, Hiromitsu First asymmetric total syntheses of fawcettimine-type Lycopodium alkaloids, lycoposerramine-C and phlegmariurine-A. Organic letters, 2009, 11, 5554-5557 |
| 1504307 | CIF | C27 H26 Br2 N2 O6 S2 | P -1 | 11.298; 11.271; 12.235 74.563; 72.728; 72.866 | 1394.2 | Shen, Ruwei; Huang, Xian Unexpected multiple electrophilic addition reaction of (Z)-alk-2-en-4-ynoates with N,N-dibromo-p-toluenesulfonamide (TsNBr(2)): a highly diastereoselective synthesis of densely functionalized aziridines. Organic letters, 2009, 11, 5698-5701 |
| 1504308 | CIF | C20 H19 Br2 N O5 S | P -1 | 7.1285; 11.5022; 13.676 98.695; 90.13; 101.33 | 1086.3 | Shen, Ruwei; Huang, Xian Unexpected multiple electrophilic addition reaction of (Z)-alk-2-en-4-ynoates with N,N-dibromo-p-toluenesulfonamide (TsNBr(2)): a highly diastereoselective synthesis of densely functionalized aziridines. Organic letters, 2009, 11, 5698-5701 |
| 1504309 | CIF | C27 H27 Br3 N2 O6 S2 | P 1 21/n 1 | 7.7972; 17.906; 22.658 90; 94.622; 90 | 3153.1 | Shen, Ruwei; Huang, Xian Unexpected multiple electrophilic addition reaction of (Z)-alk-2-en-4-ynoates with N,N-dibromo-p-toluenesulfonamide (TsNBr(2)): a highly diastereoselective synthesis of densely functionalized aziridines. Organic letters, 2009, 11, 5698-5701 |
| 1504310 | CIF | C17 H16 N2 O5 | P 1 21/c 1 | 9.6975; 17.478; 9.6297 90; 93.354; 90 | 1629.4 | Gou, Fa-Rong; Wang, Xiang-Chuan; Huo, Peng-Fei; Bi, Hai-Peng; Guan, Zheng-Hui; Liang, Yong-Min Palladium-catalyzed aryl C-H bonds activation/acetoxylation utilizing a bidentate system. Organic letters, 2009, 11, 5726-5729 |
| 1504311 | CIF | C13 H12 Cl F3 O3 | P 21 21 21 | 6.7916; 8.2807; 23.6999 90; 90; 90 | 1332.86 | Zhao, Jun-Feng; Tjan, Teguh-Budiono W; Tan, Boon-Hong; Loh, Teck-Peng Highly enantioselective ketone-ene reactions of trifluoropyruvate: significant counterion effect of the In(III)-pybox complex. Organic letters, 2009, 11, 5714-5716 |
| 1504312 | CIF | C13 H12 Br F3 O3 | P 21 21 21 | 6.8098; 8.2633; 23.9486 90; 90; 90 | 1347.62 | Zhao, Jun-Feng; Tjan, Teguh-Budiono W; Tan, Boon-Hong; Loh, Teck-Peng Highly enantioselective ketone-ene reactions of trifluoropyruvate: significant counterion effect of the In(III)-pybox complex. Organic letters, 2009, 11, 5714-5716 |
| 1504315 | CIF | C28 H25 N3 O5 S | P 21 21 21 | 9.0929; 12.3452; 22.031 90; 90; 90 | 2473.1 | Roy, Bhairab Nath; Singh, Girij Pal; Srivastava, Dhananjai; Jadhav, Harishchandra S.; Saini, Manmeet B.; Aher, Umesh P. A Novel Method for Large-Scale Synthesis of Lamivudine through Cocrystal Formation of Racemic Lamivudine with (S)-(−)-1,1′-Bi(2-naphthol) [(S)-(BINOL)] Organic Process Research & Development, 2009, 13, 450 |
| 1504316 | CIF | C9 H9 N O3 | P b c a | 16.163; 8.953; 22.95 90; 90; 90 | 3321 | Hansen, Marvin M.; Borders, Sandra S. K.; Clayton, Marcella T.; Heath, Perry C.; Kolis, Stanley P.; Larsen, Samuel D.; Linder, Ryan J.; Reutzel-Edens, Susan M.; Smith, Justin C.; Tameze, Shella L.; Ward, Jeffrey A.; Weigel, Leland O. Development of a Practical Synthesis of an Aminoindanol-Derived M1 Agonist† Organic Process Research & Development, 2009, 13, 198 |
| 1504317 | CIF | C9 H9 N O3 | C 1 2/c 1 | 16.038; 14.67; 15.634 90; 116.362; 90 | 3296 | Hansen, Marvin M.; Borders, Sandra S. K.; Clayton, Marcella T.; Heath, Perry C.; Kolis, Stanley P.; Larsen, Samuel D.; Linder, Ryan J.; Reutzel-Edens, Susan M.; Smith, Justin C.; Tameze, Shella L.; Ward, Jeffrey A.; Weigel, Leland O. Development of a Practical Synthesis of an Aminoindanol-Derived M1 Agonist† Organic Process Research & Development, 2009, 13, 198 |
| 1504318 | CIF | C21 H33 N O7 S | P 21 21 21 | 6.0017; 12.0689; 29.9339 90; 90; 90 | 2168.23 | Kopach, Michael E.; Singh, Utpal K.; Kobierski, Michael E.; Trankle, William G.; Murray, Michael M.; Pietz, Mark A.; Forst, Mindy B.; Stephenson, Gregory A.; Mancuso, Vincent; Giard, Thierry; Vanmarsenille, Michel; DeFrance, Thierry Practical Synthesis of Chiral 2-Morpholine: (4-Benzylmorpholin-2-(S)-yl)-(tetrahydropyran-4-yl)methanone Mesylate, a Useful Pharmaceutical Intermediate Organic Process Research & Development, 2009, 13, 209 |
| 1504319 | CIF | C9 H10 Cl N O | P b c a | 9.4251; 9.2575; 20.1686 90; 90; 90 | 1759.77 | Hursthouse, Michael B.; Huth, L. Susanne; Threlfall, Terence L. Why Do Organic Compounds Crystallise Well or Badly or Ever so Slowly? Why Is Crystallisation Nevertheless Such a Good Purification Technique?† Organic Process Research & Development, 2009, 13, 1231 |
| 1504320 | CIF | C11 H14 Cl N O | P b c a | 9.7381; 10.0151; 22.9501 90; 90; 90 | 2238.28 | Hursthouse, Michael B.; Huth, L. Susanne; Threlfall, Terence L. Why Do Organic Compounds Crystallise Well or Badly or Ever so Slowly? Why Is Crystallisation Nevertheless Such a Good Purification Technique?† Organic Process Research & Development, 2009, 13, 1231 |
| 1504321 | CIF | C11 H15 N O | C 1 2/c 1 | 42.887; 5.1367; 19.263 90; 108.372; 90 | 4027.3 | Hursthouse, Michael B.; Huth, L. Susanne; Threlfall, Terence L. Why Do Organic Compounds Crystallise Well or Badly or Ever so Slowly? Why Is Crystallisation Nevertheless Such a Good Purification Technique?† Organic Process Research & Development, 2009, 13, 1231 |
| 1504322 | CIF | C7 H6 Br N O | P 1 21/c 1 | 9.1595; 11.8459; 6.6063 90; 93.952; 90 | 715.1 | Hursthouse, Michael B.; Huth, L. Susanne; Threlfall, Terence L. Why Do Organic Compounds Crystallise Well or Badly or Ever so Slowly? Why Is Crystallisation Nevertheless Such a Good Purification Technique?† Organic Process Research & Development, 2009, 13, 1231 |
| 1504323 | CIF | C7 H6 Br N O | P b c a | 10.848; 9.8017; 13.5375 90; 90; 90 | 1439.43 | Hursthouse, Michael B.; Huth, L. Susanne; Threlfall, Terence L. Why Do Organic Compounds Crystallise Well or Badly or Ever so Slowly? Why Is Crystallisation Nevertheless Such a Good Purification Technique?† Organic Process Research & Development, 2009, 13, 1231 |
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