Crystallography Open Database
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Searching journal of publication like 'Organic letters' volume of publication is 8
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1506259 | CIF | C34 H41 N2 O11 | P -1 | 10.9275; 11.0354; 14.5086 92.193; 100.377; 96.85 | 1705.5 | Zhang, Aimin; Ferguson, Joseph S.; Yamato, Kazuhiro; Zheng, Chong; Gong, Bing Improving foldamer synthesis through protecting group induced unfolding of aromatic oligoamides. Organic letters, 2006, 8, 5117-5120 |
| 1506260 | CIF | C88 H118 N4 O24 | C 1 c 1 | 19.514; 16.3891; 27.727 90; 101.243; 90 | 8697.4 | Zhang, Aimin; Ferguson, Joseph S.; Yamato, Kazuhiro; Zheng, Chong; Gong, Bing Improving foldamer synthesis through protecting group induced unfolding of aromatic oligoamides. Organic letters, 2006, 8, 5117-5120 |
| 1506261 | CIF | C12 H19 N O2 | P b c a | 11.177; 14.03; 14.477 90; 90; 90 | 2270.2 | Gu, Peiming; Zhao, Yu-Ming; Tu, Yong Qiang; Ma, Yufei; Zhang, Fumin Tandem semipinacol/Schmidt reaction leading to a versatile and efficient approach to azaquaternary alkaloid skeletons. Organic letters, 2006, 8, 5271-5273 |
| 1506262 | CIF | C12 H19 N O2 | P 1 21/c 1 | 8.192; 7.778; 17.823 90; 99.82; 90 | 1119 | Gu, Peiming; Zhao, Yu-Ming; Tu, Yong Qiang; Ma, Yufei; Zhang, Fumin Tandem semipinacol/Schmidt reaction leading to a versatile and efficient approach to azaquaternary alkaloid skeletons. Organic letters, 2006, 8, 5271-5273 |
| 1506263 | CIF | C23 H32 N2 O5 | C 1 2/c 1 | 27.369; 6.226; 25.329 90; 90.231; 90 | 4316 | Arnott, Gareth; Clayden, Jonathan; Hamilton, Stuart D. Azabicyclic amino acids by stereoselective dearomatizing cyclization of the enolates of N-nicotinoyl glycine derivatives. Organic letters, 2006, 8, 5325-5328 |
| 1506264 | CIF | C23 H26 Cl3 F3 N2 O6 S | P 21 21 21 | 6.4308; 14.8616; 29.0316 90; 90; 90 | 2774.6 | Arnott, Gareth; Clayden, Jonathan; Hamilton, Stuart D. Azabicyclic amino acids by stereoselective dearomatizing cyclization of the enolates of N-nicotinoyl glycine derivatives. Organic letters, 2006, 8, 5325-5328 |
| 1506265 | CIF | C53 H69 Cl3 O12 | P -1 | 12.0169; 15.9703; 16.131 63.823; 70.256; 78.903 | 2611.45 | Salorinne, Kirsi; Nissinen, Maija Novel tetramethoxy resorcinarene bis-crown ethers. Organic letters, 2006, 8, 5473-5476 |
| 1506266 | CIF | C62 H85 N3 O14 | P -1 | 14.0187; 14.4583; 16.5822 65.075; 75.326; 77.921 | 2928.34 | Salorinne, Kirsi; Nissinen, Maija Novel tetramethoxy resorcinarene bis-crown ethers. Organic letters, 2006, 8, 5473-5476 |
| 1506267 | CIF | C60 H84 F12 K2 N2 O15 P2 | P 1 21/c 1 | 17.3738; 15.9352; 24.4132 90; 91.8; 90 | 6755.6 | Salorinne, Kirsi; Nissinen, Maija Novel tetramethoxy resorcinarene bis-crown ethers. Organic letters, 2006, 8, 5473-5476 |
| 1506268 | CIF | C62 H88 F6 Na O16 P | C 1 2/c 1 | 33.394; 15.559; 24.951 90; 101.11; 90 | 12721 | Salorinne, Kirsi; Nissinen, Maija Novel tetramethoxy resorcinarene bis-crown ethers. Organic letters, 2006, 8, 5473-5476 |
| 1506269 | CIF | C62 H88 Cl Na O20 | C 1 2/c 1 | 33.607; 15.5535; 24.7751 90; 101.153; 90 | 12705.5 | Salorinne, Kirsi; Nissinen, Maija Novel tetramethoxy resorcinarene bis-crown ethers. Organic letters, 2006, 8, 5473-5476 |
| 1506270 | CIF | C36 H26 | P 1 21/c 1 | 14.792; 10.495; 16.383 90; 95.915; 90 | 2529.8 | Lu, Jian-Mei; Shi, Min Lewis acid catalyzed reaction of arylvinylidenecyclopropanes with acetals: a facile synthetic protocol for the preparation of indene derivatives. Organic letters, 2006, 8, 5317-5320 |
| 1506271 | CIF | C38 H30 | P 1 21/c 1 | 13.4196; 11.1258; 18.781 90; 93.243; 90 | 2799.6 | Lu, Jian-Mei; Shi, Min Lewis acid catalyzed reaction of arylvinylidenecyclopropanes with acetals: a facile synthetic protocol for the preparation of indene derivatives. Organic letters, 2006, 8, 5317-5320 |
| 1506272 | CIF | C30 H37 O3 P | P -1 | 10.675; 11.455; 12.152 94.968; 95.671; 117.303 | 1299.3 | Zhang, Dong; Gao, Ruomei; Afzal, Shabana; Vargas, Mario; Sharma, Shantanu; McCurdy, Alison; Yousufuddin, Muhammed; Stewart, Timothy; Bau, Robert; Selke, Matthias Intramolecular arene epoxidation by phosphadioxiranes. Organic letters, 2006, 8, 5125-5128 |
| 1506273 | CIF | C30 H24 N O2 P | P 1 21/n 1 | 10.999; 11.201; 21.538 90; 100.571; 90 | 2608 | Zhang, Dong; Gao, Ruomei; Afzal, Shabana; Vargas, Mario; Sharma, Shantanu; McCurdy, Alison; Yousufuddin, Muhammed; Stewart, Timothy; Bau, Robert; Selke, Matthias Intramolecular arene epoxidation by phosphadioxiranes. Organic letters, 2006, 8, 5125-5128 |
| 1506274 | CIF | C24 H18 N2 O | P -1 | 7.2566; 8.17537; 16.3566 92.313; 100.627; 103.381 | 924.32 | Paravidino, Monica; Bon, Robin S.; Scheffelaar, Rachel; Vugts, Danielle J.; Znabet, Anass; Schmitz, Rob F.; de Kanter, Frans J. J.; Lutz, Martin; Spek, Anthony L.; Groen, Marinus B.; Orru, Romano V. A. Diastereoselective multicomponent synthesis of dihydropyridones with an isocyanide functionality. Organic letters, 2006, 8, 5369-5372 |
| 1506275 | CIF | C11 H10 F N S | P 1 21/c 1 | 6.5663; 7.983; 20.8615 90; 98.819; 90 | 1080.61 | Xu, Wei; Abboud, Khalil A.; Ghiviriga, Ion; Dolbier, Jr, William R; Rapp, Magdalena; Wnuk, Stanislaw F. An unexpected reaction of trimethylsilyl fluorosulfonyldifluoroacetate (TFDA) with imidazoles. Formation of N-difluoromethylthioureas. Organic letters, 2006, 8, 5549-5551 |
| 1506276 | CIF | C16 H20 Cl4 O | P 1 21/n 1 | 12.3111; 10.7924; 14.003 90; 114.56; 90 | 1692.2 | Banwell, Martin G.; Phillis, Andrew T.; Willis, Anthony C. Exploitation of cyclopropane ring-cleavage reactions for the rapid assembly of tetracyclic frameworks related to gibberellins. Organic letters, 2006, 8, 5341-5344 |
| 1506277 | CIF | C16 H20 Cl4 O | P -1 | 6.6694; 10.1604; 12.2442 100.632; 94.9445; 94.3746 | 808.83 | Banwell, Martin G.; Phillis, Andrew T.; Willis, Anthony C. Exploitation of cyclopropane ring-cleavage reactions for the rapid assembly of tetracyclic frameworks related to gibberellins. Organic letters, 2006, 8, 5341-5344 |
| 1506278 | CIF | C16 H19 Cl3 O | P 1 21/n 1 | 6.6142; 12.218; 19.1863 90; 92.6086; 90 | 1548.88 | Banwell, Martin G.; Phillis, Andrew T.; Willis, Anthony C. Exploitation of cyclopropane ring-cleavage reactions for the rapid assembly of tetracyclic frameworks related to gibberellins. Organic letters, 2006, 8, 5341-5344 |
| 1506279 | CIF | C17 H21 Cl3 O | P 1 21/n 1 | 15.7868; 6.466; 16.3562 90; 99.0435; 90 | 1648.84 | Banwell, Martin G.; Phillis, Andrew T.; Willis, Anthony C. Exploitation of cyclopropane ring-cleavage reactions for the rapid assembly of tetracyclic frameworks related to gibberellins. Organic letters, 2006, 8, 5341-5344 |
| 1506280 | CIF | C18 H21 Cl5 O | P -1 | 6.6052; 16.5809; 19.2553 111.316; 93.605; 99.927 | 1916.96 | Banwell, Martin G.; Phillis, Andrew T.; Willis, Anthony C. Exploitation of cyclopropane ring-cleavage reactions for the rapid assembly of tetracyclic frameworks related to gibberellins. Organic letters, 2006, 8, 5341-5344 |
| 1506281 | CIF | C15 H6 F6 S3 | P 1 21/a 1 | 15.461; 5.7223; 17.076 90; 96.684; 90 | 1500.49 | Ie, Yutaka; Umemoto, Yoshikazu; Kaneda, Takahiro; Aso, Yoshio Electronegative oligothiophenes based on a hexafluorocyclopentene-annelated thiophene unit. Organic letters, 2006, 8, 5381-5384 |
| 1506282 | CIF | C30 H10 F12 S6 | C 1 2/c 1 | 34.977; 5.7994; 15.474 90; 110.238; 90 | 2945.1 | Ie, Yutaka; Umemoto, Yoshikazu; Kaneda, Takahiro; Aso, Yoshio Electronegative oligothiophenes based on a hexafluorocyclopentene-annelated thiophene unit. Organic letters, 2006, 8, 5381-5384 |
| 1506283 | CIF | C30 H20 N3 O3 | P 21 21 21 | 8.463; 9.365; 26.305 90; 90; 90 | 2084.8 | Jiao, Rui H.; Xu, Shu; Liu, Jun Y.; Ge, Hui M.; Ding, Hui; Xu, Chen; Zhu, Hai L.; Tan, Ren X. Chaetominine, a cytotoxic alkaloid produced by endophytic Chaetomium sp. IFB-E015. Organic letters, 2006, 8, 5709-5712 |
| 1506284 | CIF | C20 H20 N2 O3 | P 1 21/c 1 | 12.087; 7.895; 19.07 90; 106.047; 90 | 1748.9 | Du, Yunfei; Liu, Renhe; Linn, Gregory; Zhao, Kang Synthesis of N-substituted indole derivatives via PIFA-mediated intramolecular cyclization. Organic letters, 2006, 8, 5919-5922 |
| 1506285 | CIF | C37 H52 N2 O7 | P 1 21 1 | 7.942; 10.334; 19.787 90; 92.16; 90 | 1622.8 | Kushiro, Tetsuo; Hoshino, Masaki; Tsutsumi, Takehiko; Kawai, Ken-ichi; Shiro, Motoo; Shibuya, Masaaki; Ebizuka, Yutaka Stereochemical course in water addition during LUP1-catalyzed triterpene cyclization. Organic letters, 2006, 8, 5589-5592 |
| 1506286 | CIF | C5.33 H6.22 N2.67 O0.89 S0.89 | P 1 21/c 1 | 9.397; 13.512; 13.991 90; 100.976; 90 | 1743.97 | Basheer, Ahmad; Rappoport, Zvi The first example of isomeric solid amide and its enol. Organic letters, 2006, 8, 5931-5934 |
| 1506287 | CIF | C6 H9 N3 O S | P 1 21/n 1 | 6.4264; 9.4444; 13.293 90; 96.777; 90 | 801.16 | Basheer, Ahmad; Rappoport, Zvi The first example of isomeric solid amide and its enol. Organic letters, 2006, 8, 5931-5934 |
| 1506288 | CIF | C7 H10 Cl3 N3 O S | P n a 21 | 9.2416; 8.772; 15.567 90; 90; 90 | 1262 | Basheer, Ahmad; Rappoport, Zvi The first example of isomeric solid amide and its enol. Organic letters, 2006, 8, 5931-5934 |
| 1506289 | CIF | C36 H26 N8 | P -1 | 5.646; 8.78; 14.507 104.262; 91.69; 96.25 | 691.6 | Cerna, Igor; Pohl, Radek; Klepetarová, Blanka; Hocek, Michal Direct C-H arylation of purines: development of methodology and its use in regioselective synthesis of 2,6,8-trisubstituted purines. Organic letters, 2006, 8, 5389-5392 |
| 1506290 | CIF | C25 H20 N4 | P -1 | 10.1257; 10.4037; 11.2572 101.247; 114.349; 106.926 | 963.7 | Cerna, Igor; Pohl, Radek; Klepetarová, Blanka; Hocek, Michal Direct C-H arylation of purines: development of methodology and its use in regioselective synthesis of 2,6,8-trisubstituted purines. Organic letters, 2006, 8, 5389-5392 |
| 1506291 | CIF | C29 H30 N4 O5 S | P 1 21/c 1 | 13.641; 16.424; 12.005 90; 94.29; 90 | 2682.1 | Kaiser, Hanns Martin; Lo, Wei Fun; Riahi, Abdol Majid; Spannenberg, Anke; Beller, Matthias; Tse, Man Kin New synthetic protocols for the preparation of unsymmetrical bisindoles Organic letters, 2006, 8, 5761-5764 |
| 1506292 | CIF | C17 H21 F3 O6 | P 21 21 21 | 9.6694; 13.3238; 13.8318 90; 90; 90 | 1781.99 | Sterk, Damjan; Stephan, Michel; Mohar, Barbara Highly enantioselective transfer hydrogenation of fluoroalkyl ketones. Organic letters, 2006, 8, 5935-5938 |
| 1506293 | CIF | C9 H10 F3 N O | P 21 21 21 | 6.6648; 8.1816; 18.7439 90; 90; 90 | 1022.08 | Sterk, Damjan; Stephan, Michel; Mohar, Barbara Highly enantioselective transfer hydrogenation of fluoroalkyl ketones. Organic letters, 2006, 8, 5935-5938 |
| 1506294 | CIF | C88 H16 F40 O8 | P 1 21/c 1 | 16.871; 22.046; 22.462 90; 103.148; 90 | 8135 | Reddy, J. Sreedhar; Mandal, Sukhendu; Anand, Venkataramanarao G. Cyclic oligofurans: one-pot synthesis of 30pi and 40pi expanded porphyrinoids. Organic letters, 2006, 8, 5541-5543 |
| 1506295 | CIF | C12 H9 N3 | P 21 21 21 | 5.1126; 13.096; 14.347 90; 90; 90 | 960.6 | Shibahara, Fumitoshi; Kitagawa, Asumi; Yamaguchi, Eiji; Murai, Toshiaki Synthesis of 2-azaindolizines by using an iodine-mediated oxidative desulfurization promoted cyclization of N-2-pyridylmethyl thioamides and an investigation of their photophysical properties. Organic letters, 2006, 8, 5621-5624 |
| 1506296 | CIF | C24 H16 N6 S | P -1 | 8.049; 10.286; 12.388 90.925; 101.862; 98.595 | 991.3 | Shibahara, Fumitoshi; Kitagawa, Asumi; Yamaguchi, Eiji; Murai, Toshiaki Synthesis of 2-azaindolizines by using an iodine-mediated oxidative desulfurization promoted cyclization of N-2-pyridylmethyl thioamides and an investigation of their photophysical properties. Organic letters, 2006, 8, 5621-5624 |
| 1506297 | CIF | C17 H14 N2 O S | P -1 | 9.642; 9.953; 16.2792 97.093; 92.531; 97.689 | 1533.44 | Singh, C. B.; Murru, Siva; Kavala, Veerababurao; Patel, Bhisma K. It is "thiazolidene-2-imine" and not imidazole-2-thione as the reaction product of 1-benzoyl-3-phenylthiourea with Br(2)/enolizable ketone. Organic letters, 2006, 8, 5397-5399 |
| 1506298 | CIF | C22 H16 N2 O S | P 1 21/n 1 | 10.4679; 15.2299; 11.7243 90; 101.491; 90 | 1831.7 | Singh, C. B.; Murru, Siva; Kavala, Veerababurao; Patel, Bhisma K. It is "thiazolidene-2-imine" and not imidazole-2-thione as the reaction product of 1-benzoyl-3-phenylthiourea with Br(2)/enolizable ketone. Organic letters, 2006, 8, 5397-5399 |
| 1506299 | CIF | C17 H13 Br N2 O S | P 1 21/c 1 | 16.059; 13.4006; 7.6695 90; 98.68; 90 | 1631.6 | Singh, C. B.; Murru, Siva; Kavala, Veerababurao; Patel, Bhisma K. It is "thiazolidene-2-imine" and not imidazole-2-thione as the reaction product of 1-benzoyl-3-phenylthiourea with Br(2)/enolizable ketone. Organic letters, 2006, 8, 5397-5399 |
| 1506300 | CIF | C12 H15 N O3 | P 1 21/n 1 | 10.9577; 9.0799; 11.3076 90; 96.931; 90 | 1116.8 | Malona, John A.; Colbourne, Jessica M.; Frontier, Alison J. A general method for the catalytic nazarov cyclization of heteroaromatic compounds. Organic letters, 2006, 8, 5661-5664 |
| 1506301 | CIF | C21 H24 O6 | P 1 21/c 1 | 11.0511; 20.5371; 9.0441 90; 96.047; 90 | 2041.2 | Duan, Xin-Hua; Guo, Li-Na; Bi, Hai-Peng; Liu, Xue-Yuan; Liang, Yong-Min Highly regioselective synthesis of 2,3-disubstituted indenes via a novel palladium-catalyzed cyclization reaction of propargylic carbonates with carbon nucleophiles. Organic letters, 2006, 8, 5777-5780 |
| 1506302 | CIF | C15 H16 O5 | P -1 | 8.193; 8.974; 18.504 89.169; 81.157; 72.754 | 1283.2 | Pittelkow, Michael; Boas, Ulrik; Christensen, Jørn B Carbocations in action. Design, synthesis, and evaluation of a highly acid-sensitive naphthalene-based backbone amide linker for solid-phase synthesis. Organic letters, 2006, 8, 5817-5820 |
| 1506303 | CIF | C19 H16 O5 | P 1 21/c 1 | 7.764; 21.989; 8.721 90; 94.738; 90 | 1483.8 | Dahl, Bart J.; Branchaud, Bruce P. 180 degree unidirectional bond rotation in a biaryl lactone artificial molecular motor prototype. Organic letters, 2006, 8, 5841-5844 |
| 1506304 | CIF | C22 H18 F6 N4 O8 Pd2 S2 | P -1 | 7.7003; 12.9161; 14.763 87.536; 84.658; 74.544 | 1408.8 | Zhao, Baowei; Lu, Xiyan Cationic palladium(II)-catalyzed addition of arylboronic acids to nitriles. One-step synthesis of benzofurans from phenoxyacetonitriles. Organic letters, 2006, 8, 5987-5990 |
| 1506305 | CIF | C46.38 H37 Cl2.76 N10 O2 | P -1 | 16.654; 17.694; 17.91 77.62; 64.1; 89.91 | 4612 | Wang, Qi-Qiang; Wang, De-Xian; Ma, Hong-Wei; Wang, Mei-Xiang Synthesis of tetraazacalix[2]arene[2]triazines: tuning the cavity by the substituents on the bridging nitrogen atoms. Organic letters, 2006, 8, 5967-5970 |
| 1506306 | CIF | C33.5 H27.5 Cl2 N10.5 O2.5 | P -1 | 13.477; 15.305; 16.878 76.66; 89.07; 88.22 | 3385.6 | Wang, Qi-Qiang; Wang, De-Xian; Ma, Hong-Wei; Wang, Mei-Xiang Synthesis of tetraazacalix[2]arene[2]triazines: tuning the cavity by the substituents on the bridging nitrogen atoms. Organic letters, 2006, 8, 5967-5970 |
| 1506307 | CIF | C32 H24 Cl2 N10 | P n a 21 | 13.007; 14.042; 16.794 90; 90; 90 | 3067.3 | Wang, Qi-Qiang; Wang, De-Xian; Ma, Hong-Wei; Wang, Mei-Xiang Synthesis of tetraazacalix[2]arene[2]triazines: tuning the cavity by the substituents on the bridging nitrogen atoms. Organic letters, 2006, 8, 5967-5970 |
| 1506308 | CIF | C51 H50 Cl2 N12 O4 | C 1 2/c 1 | 26.598; 9.4281; 20.033 90; 110.21; 90 | 4714.4 | Wang, Qi-Qiang; Wang, De-Xian; Ma, Hong-Wei; Wang, Mei-Xiang Synthesis of tetraazacalix[2]arene[2]triazines: tuning the cavity by the substituents on the bridging nitrogen atoms. Organic letters, 2006, 8, 5967-5970 |
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