Crystallography Open Database
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Result: there are 907 entries in the selection
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Searching journal of publication like 'Organic letters' volume of publication is 16
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
---|---|---|---|---|---|---|
1517201 | CIF | C13 H16 N2 O2 S | P 1 21/c 1 | 8.3852; 14.3202; 11.2113 90; 105.908; 90 | 1294.67 | Chen, Bo; Scott, Mark E.; Adams, Bruce A.; Hrovat, David A.; Borden, Weston Thatcher; Lautens, Mark Computational and (13)C Investigations of the Diazadienes and Oxazadienes Formed via the Rearrangement of Methylenecyclopropyl Hydrazones and Oximes. Organic letters, 2014, 16, 3930-3933 |
1517203 | CIF | C53 H46 Cl4 N2 O P2 Ru | P 1 21 1 | 11.20234; 14.9864; 14.7402 90; 107.993; 90 | 2353.6 | Chen, Xiangning; Zhou, Han; Zhang, Kunyu; Li, Jiawen; Huang, Hanmin Highly enantioselective hydrogenation of steric hindrance enones catalyzed by ru complexes with chiral diamine and achiral phosphane. Organic letters, 2014, 16, 3912-3915 |
1517204 | CIF | C29 H30 N4 O3 | P -1 | 8.3324; 11.148; 14.586 109.23; 99.14; 103.7 | 1200.8 | Wang, Kai-Bo; Di, Ying-Tong; Bao, Yu; Yuan, Chun-Mao; Chen, Gang; Li, Da-Hong; Bai, Jiao; He, Hong-Ping; Hao, Xiao-Jiang; Pei, Yue-Hu; Jing, Yong-Kui; Li, Zhan-Lin; Hua, Hui-Ming Peganumine A, a β-Carboline Dimer with a New Octacyclic Scaffold from Peganum harmala. Organic letters, 2014, 16, 4028-4031 |
1517205 | CIF | C22 H25 N O3 | P -1 | 9.615; 10.042; 10.834 87.159; 87.752; 73.682 | 1002.3 | Yan, Zhi-Ming; Wu, Na; Liang, Dong; Wang, Heng-Shan; Pan, Ying-Ming One-Pot Stepwise Approach to β-Enaminoketoesters through "Masked" 1,3-Aza-Dipoles. Organic letters, 2014, 16, 4048-4051 |
1517217 | CIF | C22 H18 N2 O3 | P 1 21/n 1 | 14.0236; 6.7864; 19.674 90; 104.499; 90 | 1812.7 | Nakamura, Itaru; Onuma, Toshiki; Kanazawa, Ryo; Nishigai, Yuki; Terada, Masahiro Efficient Synthesis of N-Alkylated α,β-Unsaturated Ketonitrones via Cu-Catalyzed Rearrangement. Organic letters, 2014, 16, 4198-4200 |
1517218 | CIF | C15 H18 O3 | P 21 21 21 | 6.8426; 12.785; 29.768 90; 90; 90 | 2604.2 | Chuang, Hsiang-Yu; Isobe, Minoru Novel synthesis of right segment of solanoeclepin a. Organic letters, 2014, 16, 4166-4169 |
1517219 | CIF | C15 H22 O5 | P 21 21 21 | 7.2566; 10.5786; 19.4869 90; 90; 90 | 1495.91 | Chuang, Hsiang-Yu; Isobe, Minoru Novel synthesis of right segment of solanoeclepin a. Organic letters, 2014, 16, 4166-4169 |
1517222 | CIF | C16 H10 O2 Se3 | P 1 21/c 1 | 17.967; 6.0336; 14.479 90; 96.147; 90 | 1560.6 | Maity, Pintu; Kundu, Debasish; Roy, Rajdip; Ranu, Brindaban C. A direct synthesis of selenophenes by cu-catalyzed one-pot addition of a selenium moiety to (e,e)-1,3-dienyl bromides and subsequent nucleophilic cyclization. Organic letters, 2014, 16, 4122-4125 |
1517228 | CIF | C20 H23 Cl2 N O2 Pd S | P 21 21 21 | 10.1386; 14.3557; 14.5248 90; 90; 90 | 2114 | Kondo, Hiroki; Yu, Feng; Yamaguchi, Junichiro; Liu, Guosheng; Itami, Kenichiro Branch-Selective Allylic C-H Carboxylation of Terminal Alkenes by Pd/sox Catalyst. Organic letters, 2014, 16, 4212-4215 |
1517229 | CIF | C20 H32 O3 | P 32 2 1 | 17.4587; 17.4587; 10.7319 90; 90; 120 | 2832.9 | Clark, J. Stephen; Delion, Laetitia; Farrugia, Louis J. Total synthesis of the purported structure of sclerophytin f. Organic letters, 2014, 16, 4300-4303 |
1517230 | CIF | C18 H26 O4 | P -1 | 8.1038; 13.1776; 16.2542 71.565; 85.809; 75.309 | 1592.81 | Clark, J. Stephen; Delion, Laetitia; Farrugia, Louis J. Total synthesis of the purported structure of sclerophytin f. Organic letters, 2014, 16, 4300-4303 |
1517231 | CIF | C20 H32 O4 | P 21 21 21 | 5.624; 16.55; 19.16 90; 90; 90 | 1783.4 | Clark, J. Stephen; Delion, Laetitia; Farrugia, Louis J. Total synthesis of the purported structure of sclerophytin f. Organic letters, 2014, 16, 4300-4303 |
1517232 | CIF | C16 H23 N O2 S | P 1 21 1 | 5.526; 11.111; 13.716 90; 98.463; 90 | 833 | Su, Lin; Zhu, Ting-Shun; Xu, Ming-Hua Indium-Mediated Asymmetric Intramolecular Allenylation of N-tert-Butanesulfinyl Imines: Efficient and Practical Access to Chiral 3-Allenyl-4-aminochromanes. Organic letters, 2014, 16, 4118-4121 |
1517233 | CIF | C19 H21 N O3 S | P 1 | 7.176; 10.859; 12.059 100.648; 106.125; 95.565 | 876.2 | Su, Lin; Zhu, Ting-Shun; Xu, Ming-Hua Indium-Mediated Asymmetric Intramolecular Allenylation of N-tert-Butanesulfinyl Imines: Efficient and Practical Access to Chiral 3-Allenyl-4-aminochromanes. Organic letters, 2014, 16, 4118-4121 |
1517234 | CIF | C16 H17 N O2 S | C 1 2 1 | 19.1174; 6.6815; 13.5889 90; 110.988; 90 | 1620.59 | Su, Lin; Zhu, Ting-Shun; Xu, Ming-Hua Indium-Mediated Asymmetric Intramolecular Allenylation of N-tert-Butanesulfinyl Imines: Efficient and Practical Access to Chiral 3-Allenyl-4-aminochromanes. Organic letters, 2014, 16, 4118-4121 |
1517235 | CIF | C19 H21 N O3 S | P 1 21 1 | 11.8178; 6.1413; 12.0958 90; 95.858; 90 | 873.29 | Su, Lin; Zhu, Ting-Shun; Xu, Ming-Hua Indium-Mediated Asymmetric Intramolecular Allenylation of N-tert-Butanesulfinyl Imines: Efficient and Practical Access to Chiral 3-Allenyl-4-aminochromanes. Organic letters, 2014, 16, 4118-4121 |
1517236 | CIF | C14 H13 N O5 | P b c a | 6.9386; 15.1121; 23.6998 90; 90; 90 | 2485.09 | Logan, Angus W. J.; Sprague, Simon J.; Foster, Robert W.; Marx, Léo B; Garzya, Vincenzo; Hallside, Michal S.; Thompson, Amber L.; Burton, Jonathan W. Diastereoselective synthesis of fused lactone-pyrrolidinones; application to a formal synthesis of (-)-salinosporamide a. Organic letters, 2014, 16, 4078-4081 |
1517237 | CIF | C26 H35 N O6 | P 21 21 21 | 6.2769; 19.0465; 20.3494 90; 90; 90 | 2432.83 | Logan, Angus W. J.; Sprague, Simon J.; Foster, Robert W.; Marx, Léo B; Garzya, Vincenzo; Hallside, Michal S.; Thompson, Amber L.; Burton, Jonathan W. Diastereoselective synthesis of fused lactone-pyrrolidinones; application to a formal synthesis of (-)-salinosporamide a. Organic letters, 2014, 16, 4078-4081 |
1517247 | CIF | C21 H23 N O4 | P 1 21 1 | 9.6514; 13.5727; 28.8023 90; 99.6158; 90 | 3720 | Azuma, Takumi; Murata, Akihiro; Kobayashi, Yusuke; Inokuma, Tsubasa; Takemoto, Yoshiji A Dual Arylboronic Acid-Aminothiourea Catalytic System for the Asymmetric Intramolecular Hetero-Michael Reaction of α,β-Unsaturated Carboxylic Acids. Organic letters, 2014, 16, 4256-4259 |
1517248 | CIF | C10 H12 O4 | I 41/a :2 | 19.225; 19.225; 10.568 90; 90; 90 | 3906 | Kasare, Sanghratna; Bankar, Siddheshwar K.; Ramasastry, S. S. V. Expeditious Metal-Free Access to Functionalized Polycyclic Acetals under Mild Aqueous Conditions. Organic letters, 2014, 16, 4284-4287 |
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