Crystallography Open Database
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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 |
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1513433 | CIF | C18 H14 N2 O3 | P -1 | 6.0877; 10.9989; 11.2984 83.29; 87.571; 83.717 | 746.49 | Hao, Xin-Qi; Chen, Li-Juan; Ren, Baozeng; Li, Liu-Yan; Yang, Xin-Yan; Gong, Jun-Fang; Niu, Jun-Long; Song, Mao-Ping Copper-mediated direct aryloxylation of benzamides assisted by an n,o-bidentate directing group. Organic letters, 2014, 16, 1104-1107 |
1513434 | CIF | C24 H18 N2 O4 | P -1 | 7.2876; 12.0282; 12.8131 115.87; 93.712; 98.655 | 988.3 | Hao, Xin-Qi; Chen, Li-Juan; Ren, Baozeng; Li, Liu-Yan; Yang, Xin-Yan; Gong, Jun-Fang; Niu, Jun-Long; Song, Mao-Ping Copper-mediated direct aryloxylation of benzamides assisted by an n,o-bidentate directing group. Organic letters, 2014, 16, 1104-1107 |
1513435 | CIF | C37 H33 F3 N O4 Rh S | P -1 | 11.015; 12.485; 13.435 102.315; 110.462; 93.671 | 1672 | Yu, Songjie; Li, Xingwei Mild Synthesis of Chalcones via Rhodium(III)-Catalyzed C-C Coupling of Arenes and Cyclopropenones. Organic letters, 2014, 16, 1220-1223 |
1513436 | CIF | C26 H19 N O | P -1 | 10.7315; 13.8056; 14.032 89.874; 88.794; 68.616 | 1935.33 | Yu, Songjie; Li, Xingwei Mild Synthesis of Chalcones via Rhodium(III)-Catalyzed C-C Coupling of Arenes and Cyclopropenones. Organic letters, 2014, 16, 1220-1223 |
1513437 | CIF | C21 H18 O3 | P -1 | 8.9589; 9.9488; 10.2552 115.145; 98.6848; 96.7865 | 800.79 | Teo, Wan Teng; Rao, Weidong; Ng, Charmaine Jia Huan; Koh, Shaun Wei Yong; Chan, Philip Wai Hong Gold-Catalyzed Benzannulation of 5-Hydroxy-3-oxoalk-6-ynoate Esters to o-Phenolic Esters. Organic letters, 2014, 16, 1248-1251 |
1513438 | CIF | C12 H11 F3 N4 O2 S | P 1 21/c 1 | 9.7909; 9.9299; 15.0054 90; 108.195; 90 | 1385.92 | Qiao, Zongjun; Wei, Jianpeng; Jiang, Xuefeng Direct Cross-Coupling Access to Diverse Aromatic Sulfide: Palladium-Catalyzed Double C-S Bond Construction Using Na2S2O3 as a Sulfurating Reagent. Organic letters, 2014, 16, 1212-1215 |
1513439 | CIF | C17 H26 N2 O2 | P 1 21/c 1 | 13.224; 6.1677; 22.599 90; 118.413; 90 | 1621.2 | Luescher, Michael U.; Vo, Cam-Van T; Bode, Jeffrey W. SnAP Reagents for the Synthesis of Piperazines and Morpholines. Organic letters, 2014, 16, 1236-1239 |
1513440 | CIF | C13 H20 N2 O | P 1 21/c 1 | 9.62; 6.3559; 20.787 90; 107.642; 90 | 1211.2 | Luescher, Michael U.; Vo, Cam-Van T; Bode, Jeffrey W. SnAP Reagents for the Synthesis of Piperazines and Morpholines. Organic letters, 2014, 16, 1236-1239 |
1513441 | CIF | C20 H29 N3 O2 | P 21 21 21 | 10.1265; 10.6178; 18.064 90; 90; 90 | 1942.26 | Kapras, Vojtěch; Pohl, Radek; Císařová, Ivana; Jahn, Ullrich Asymmetric Domino Aza-Michael Addition/[3 + 2] Cycloaddition Reactions as a Versatile Approach to α,β,γ-Triamino Acid Derivatives. Organic letters, 2014, 16, 1088-1091 |
1513442 | CIF | C20 H29 N3 O2 | P 21 21 21 | 8.2352; 9.944; 23.9419 90; 90; 90 | 1960.62 | Kapras, Vojtěch; Pohl, Radek; Císařová, Ivana; Jahn, Ullrich Asymmetric Domino Aza-Michael Addition/[3 + 2] Cycloaddition Reactions as a Versatile Approach to α,β,γ-Triamino Acid Derivatives. Organic letters, 2014, 16, 1088-1091 |
1513443 | CIF | C24 H32 N O2.5 S Si | P 1 21 1 | 15.6508; 6.3555; 24.6704 90; 101.826; 90 | 2401.85 | Fustero, Santos; Lázaro, Rubén; Aiguabella, Nuria; Riera, Antoni; Simón-Fuentes, Antonio; Barrio, Pablo Asymmetric allylation/Pauson-Khand reaction: a simple entry to polycyclic amines. Application to the synthesis of aminosteroid analogues Organic Letters, 2014, 16, 1224-1227 |
1513444 | CIF | C24 H29 N O3 S | P 21 21 21 | 5.86956; 16.1458; 22.8868 90; 90; 90 | 2168.95 | Fustero, Santos; Lázaro, Rubén; Aiguabella, Nuria; Riera, Antoni; Simón-Fuentes, Antonio; Barrio, Pablo Asymmetric allylation/Pauson-Khand reaction: a simple entry to polycyclic amines. Application to the synthesis of aminosteroid analogues Organic Letters, 2014, 16, 1224-1227 |
1513445 | CIF | C70 H78 N2 | C 1 2 1 | 33.2464; 6.863; 31.448 90; 109.185; 90 | 6777 | Castro-Fernández, Silvia; Lahoz, Inmaculada R.; Llamas-Saiz, Antonio L; Alonso-Gómez, José Lorenzo; Cid, María-Magdalena; Navarro-Vázquez, Armando Preparation and Characterization of a Halogen-Bonded Shape-Persistent Chiral Alleno-acetylenic Inclusion Complex. Organic letters, 2014, 16, 1136-1139 |
1513446 | CIF | C74 H78 F8 I2 N2 | P 1 | 14.078; 15.968; 16.71 107.796; 101.993; 90.015 | 3490.3 | Castro-Fernández, Silvia; Lahoz, Inmaculada R.; Llamas-Saiz, Antonio L; Alonso-Gómez, José Lorenzo; Cid, María-Magdalena; Navarro-Vázquez, Armando Preparation and Characterization of a Halogen-Bonded Shape-Persistent Chiral Alleno-acetylenic Inclusion Complex. Organic letters, 2014, 16, 1136-1139 |
1513447 | CIF | C16 H18 N2 O3 | P 1 21 1 | 8.891; 9.473; 9.472 90; 110.488; 90 | 747.31 | Holmquist, Melireth; Blay, Gonzalo; Muñoz, M Carmen; Pedro, José R Enantioselective addition of nitromethane to 2-acylpyridine N-oxides. Expanding the generation of quaternary stereocenters with the Henry reaction. Organic letters, 2014, 16, 1204-1207 |
1513448 | CIF | C32 H56 Cu2 I2 N2 P2 | P 1 21/c 1 | 9.5602; 10.0738; 20.0433 90; 103.413; 90 | 1877.7 | Gurung, Santosh K.; Thapa, Surendra; Kafle, Arjun; Dickie, Diane A.; Giri, Ramesh Copper-Catalyzed Suzuki-Miyaura Coupling of Arylboronate Esters: Transmetalation with (PN)CuF and Identification of Intermediates. Organic letters, 2014, 16, 1264-1267 |
1513449 | CIF | C32 H56 Cu2 F2 N2 P2 | P -1 | 8.4927; 8.7287; 12.6862 86.989; 76.97; 68.516 | 852.1 | Gurung, Santosh K.; Thapa, Surendra; Kafle, Arjun; Dickie, Diane A.; Giri, Ramesh Copper-Catalyzed Suzuki-Miyaura Coupling of Arylboronate Esters: Transmetalation with (PN)CuF and Identification of Intermediates. Organic letters, 2014, 16, 1264-1267 |
1513450 | CIF | C22 H33 Cu N P | P n a 21 | 18.6292; 9.3181; 12.5012 90; 90; 90 | 2170.1 | Gurung, Santosh K.; Thapa, Surendra; Kafle, Arjun; Dickie, Diane A.; Giri, Ramesh Copper-Catalyzed Suzuki-Miyaura Coupling of Arylboronate Esters: Transmetalation with (PN)CuF and Identification of Intermediates. Organic letters, 2014, 16, 1264-1267 |
1513451 | CIF | C18 H15 N O7 | P c c n | 30.1051; 30.0687; 7.05381 90; 90; 90 | 6385.3 | Jolibois, Alexandre E. R.; Lewis, William; Moody, Christopher J. Total synthesis of (±)-distomadines a and B. Organic letters, 2014, 16, 1064-1067 |
1513452 | CIF | C31 H36 D4 N4 O12 | P -1 | 8.2246; 10.2692; 19.3753 87.895; 83.248; 88.205 | 1623.39 | Jolibois, Alexandre E. R.; Lewis, William; Moody, Christopher J. Total synthesis of (±)-distomadines a and B. Organic letters, 2014, 16, 1064-1067 |
1513453 | CIF | C26 H25 N O7 | P -1 | 7.8031; 9.1491; 16.0757 77.259; 83.756; 78.585 | 1094.72 | Jolibois, Alexandre E. R.; Lewis, William; Moody, Christopher J. Total synthesis of (±)-distomadines a and B. Organic letters, 2014, 16, 1064-1067 |
1513454 | CIF | C28 H24 O3 | P 1 21/c 1 | 10.2556; 24.4715; 9.0713 90; 106.55; 90 | 2182.3 | Shen, Ruwei; Chen, Ke; Deng, Qiulin; Yang, Jianjun; Zhang, Lixiong Highly Stereoselective Generation of Complex Oxy-Bicyclic Scaffolds via an Atom-Economic Pd(II)-Catalyzed Hydroalkynylation, Isomerization and Diels-Alder Cycloaddition Sequence. Organic letters, 2014, 16, 1208-1211 |
1513455 | CIF | C24 H23 N O4 | P 1 21/c 1 | 14.8441; 7.7448; 18.0075 90; 113.215; 90 | 1902.6 | Viswambharan, Baby; Gori, Didier; Guillot, Régis; Kouklovsky, Cyrille; Alezra, Valérie Substrate Control in Enantioselective and Diastereoselective Aldol Reaction by Memory of Chirality: A Rapid Access to Enantiopure β-Hydroxy Quaternary α-Amino Acids. Organic letters, 2014, 16, 788-791 |
1513456 | CIF | C24 H22 Br N O4 | P 21 21 21 | 8.0051; 17.9833; 28.7749 90; 90; 90 | 4142.4 | Viswambharan, Baby; Gori, Didier; Guillot, Régis; Kouklovsky, Cyrille; Alezra, Valérie Substrate Control in Enantioselective and Diastereoselective Aldol Reaction by Memory of Chirality: A Rapid Access to Enantiopure β-Hydroxy Quaternary α-Amino Acids. Organic letters, 2014, 16, 788-791 |
1513457 | CIF | C24 H22 Br N O4 | P 1 21 1 | 9.9229; 10.8841; 9.9414 90; 99.819; 90 | 1057.96 | Viswambharan, Baby; Gori, Didier; Guillot, Régis; Kouklovsky, Cyrille; Alezra, Valérie Substrate Control in Enantioselective and Diastereoselective Aldol Reaction by Memory of Chirality: A Rapid Access to Enantiopure β-Hydroxy Quaternary α-Amino Acids. Organic letters, 2014, 16, 788-791 |
1513458 | CIF | C24 H22 F N O4 | P 1 21 1 | 9.4102; 10.467; 10.3023 90; 98.469; 90 | 1003.68 | Viswambharan, Baby; Gori, Didier; Guillot, Régis; Kouklovsky, Cyrille; Alezra, Valérie Substrate Control in Enantioselective and Diastereoselective Aldol Reaction by Memory of Chirality: A Rapid Access to Enantiopure β-Hydroxy Quaternary α-Amino Acids. Organic letters, 2014, 16, 788-791 |
1513459 | CIF | C22 H21 N O5 | P 21 21 2 | 8.3847; 26.3518; 8.3634 90; 90; 90 | 1847.91 | Viswambharan, Baby; Gori, Didier; Guillot, Régis; Kouklovsky, Cyrille; Alezra, Valérie Substrate Control in Enantioselective and Diastereoselective Aldol Reaction by Memory of Chirality: A Rapid Access to Enantiopure β-Hydroxy Quaternary α-Amino Acids. Organic letters, 2014, 16, 788-791 |
1513460 | CIF | C37 H36 N2 O4 S | P 21 21 21 | 9.2689; 11.8049; 29.331 90; 90; 90 | 3209.35 | Rao, V. U. Bhaskara; Jadhav, Amol P.; Garad, Dnyaneshwar; Singh, Ravi P. Asymmetric Vinylogous Mannich Reaction of Silyloxy Furans with N-tert-Butanesulfinyl Ketimines. Organic letters, 2014, 16, 648-651 |
1513461 | CIF | C13 H9 F3 O2 S | P -1 | 5.119; 8.73; 14.233 74.729; 80.666; 79.881 | 599.5 | Yasu, Yusuke; Arai, Yusuke; Tomita, Ren; Koike, Takashi; Akita, Munetaka Highly Regio- and Diastereoselective Synthesis of CF3-Substituted Lactones via Photoredox-Catalyzed Carbolactonization of Alkenoic Acids. Organic letters, 2014, 16, 780-783 |
1513462 | CIF | C14 H15 F3 O2 | P 1 21 1 | 9.664; 10.003; 14.245 90; 109.73; 90 | 1296.2 | Yasu, Yusuke; Arai, Yusuke; Tomita, Ren; Koike, Takashi; Akita, Munetaka Highly Regio- and Diastereoselective Synthesis of CF3-Substituted Lactones via Photoredox-Catalyzed Carbolactonization of Alkenoic Acids. Organic letters, 2014, 16, 780-783 |
1513463 | CIF | C23 H18 O4 | P -1 | 5.1782; 11.752; 14.9599 69.088; 80.195; 83.679 | 836.78 | Bhojgude, Sachin Suresh; Bhunia, Anup; Gonnade, Rajesh G.; Biju, Akkattu T. Efficient synthesis of 9-aryldihydrophenanthrenes by a cascade reaction involving arynes and styrenes. Organic letters, 2014, 16, 676-679 |
1513464 | CIF | C27 H23 Br O3 S | C 1 2 1 | 31.361; 5.4611; 13.461 90; 91.404; 90 | 2304.7 | Wang, Shengzheng; Zhang, Yongqiang; Dong, Guoqiang; Wu, Shanchao; Fang, Kun; Li, Zhengang; Miao, Zhenyuan; Yao, Jianzhong; Li, Hao; Li, Jian; Zhang, Wannian; Wang, Wei; Sheng, Chunquan Facile Assembly of Chiral Tetrahydrothiopyrans Containing Four Consecutive Stereocenters via an Organocatalytic Enantioselective Michael-Michael Cascade. Organic letters, 2014, 16, 692-695 |
1513465 | CIF | C91.5 H93.48 N6 O2 Zn | P -1 | 14.6574; 15.6368; 17.2398 98.501; 92.026; 92.976 | 3898.9 | Fujimoto, Keisuke; Yorimitsu, Hideki; Osuka, Atsuhiro Facile Preparation of β-Haloporphyrins as Useful Precursors of β-Substituted Porphyrins. Organic letters, 2014, 16, 972-975 |
1513466 | CIF | C70 H82 I2 N4 O Zn | P 1 21 1 | 13.0277; 17.4618; 15.417 90; 112.166; 90 | 3247.97 | Fujimoto, Keisuke; Yorimitsu, Hideki; Osuka, Atsuhiro Facile Preparation of β-Haloporphyrins as Useful Precursors of β-Substituted Porphyrins. Organic letters, 2014, 16, 972-975 |
1513467 | CIF | C69 H79 Cl3 N7 O Zn | P -1 | 9.4123; 18.6641; 20.8623 111.756; 102.842; 97.3951 | 3227.3 | Fujimoto, Keisuke; Yorimitsu, Hideki; Osuka, Atsuhiro Facile Preparation of β-Haloporphyrins as Useful Precursors of β-Substituted Porphyrins. Organic letters, 2014, 16, 972-975 |
1513468 | CIF | C30 H27 Cl N2 O4 S | P 1 21/n 1 | 13.995; 10.384; 18.902 90; 101.9; 90 | 2688 | Zheng, Chen; Chen, Jin Jin; Fan, Renhua Dearomatization Strategy and Palladium-Catalyzed Domino Reaction: Construction of Azepino[5,4,3-cd]indoles from 2-Alkynylanilines. Organic letters, 2014, 16, 816-819 |
1513469 | CIF | C38 H28 F6 N2 O4 | P -1 | 11.1314; 11.2899; 12.8198 97.378; 98.233; 107.436 | 1495.98 | Roznyatovskiy, Vladimir V.; Gardner, Daniel M.; Eaton, Samuel W.; Wasielewski, Michael R. Radical anions of trifluoromethylated perylene and naphthalene imide and diimide electron acceptors. Organic letters, 2014, 16, 696-699 |
1513470 | CIF | C32 H36 F6 N2 O4 | P -1 | 4.9874; 8.9169; 16.946 85.639; 82.595; 81.82 | 738.46 | Roznyatovskiy, Vladimir V.; Gardner, Daniel M.; Eaton, Samuel W.; Wasielewski, Michael R. Radical anions of trifluoromethylated perylene and naphthalene imide and diimide electron acceptors. Organic letters, 2014, 16, 696-699 |
1513471 | CIF | C15 H14 O5 | P 1 21/c 1 | 3.8624; 15.954; 20.21 90; 94.944; 90 | 1240.7 | Manikandan, Rajendran; Jeganmohan, Masilamani Ruthenium-Catalyzed Dimerization of Propiolates: A Simple Route to α-Pyrones. Organic letters, 2014, 16, 652-655 |
1513472 | CIF | C20 H14 O4 | P 1 21/n 1 | 10.0981; 8.6701; 18.677 90; 93.607; 90 | 1632 | Manikandan, Rajendran; Jeganmohan, Masilamani Ruthenium-Catalyzed Dimerization of Propiolates: A Simple Route to α-Pyrones. Organic letters, 2014, 16, 652-655 |
1513473 | CIF | C21 H30 O6 | P 21 21 2 | 23.138; 24.004; 8.6874 90; 90; 90 | 4825 | Gao, Xiu; Shao, Li-Dong; Dong, Liao-Bin; Cheng, Xiao; Wu, Xing-De; Liu, Fei; Jiang, Wei-Wei; Peng, Li-Yan; He, Juan; Zhao, Qin-Shi Vibsatins A and B, Two New Tetranorvibsane-Type Diterpenoids from Viburnum tinus cv. variegatus. Organic letters, 2014, 16, 980-983 |
1513474 | CIF | C21 H26 O8 | P 1 21/n 1 | 21.692; 8.7516; 22.332 90; 101.726; 90 | 4151 | Yamamoto, Mitsuaki; Hayashi, Shunsuke; Isa, Kazuki; Kawatsura, Motoi Palladium-Catalyzed Double Alkylation of 3-Aryl-2-fluoroallyl Esters with Malonate Nucleophiles through the Carbon-Fluorine Bond Cleavage. Organic letters, 2014, 16, 700-703 |
1513475 | CIF | C42 H45 N2 O2 P | P 1 21/n 1 | 14.3562; 14.8127; 17.4328 90; 110.316; 90 | 3476.5 | Chase, Daniel T.; Moerdyk, Jonathan P.; Bielawski, Christopher W. Exploring the chemistry of n,n'-diamidocarbenes with organophosphorus compounds. Organic letters, 2014, 16, 812-815 |
1513476 | CIF | C24 H28 N2 O2 | P 1 21/c 1 | 17.07; 16.146; 7.7572 90; 91.011; 90 | 2137.6 | Chase, Daniel T.; Moerdyk, Jonathan P.; Bielawski, Christopher W. Exploring the chemistry of n,n'-diamidocarbenes with organophosphorus compounds. Organic letters, 2014, 16, 812-815 |
1513477 | CIF | C25 H30 N2 O2 | P 1 21/c 1 | 8.441; 16.218; 15.825 90; 96.725; 90 | 2151 | Chase, Daniel T.; Moerdyk, Jonathan P.; Bielawski, Christopher W. Exploring the chemistry of n,n'-diamidocarbenes with organophosphorus compounds. Organic letters, 2014, 16, 812-815 |
1513478 | CIF | C13 H17 Br O3 | P 1 21/c 1 | 7.7491; 32.258; 10.4006 90; 90.016; 90 | 2599.8 | Shen, Zhi-Liang; Peng, Zhihua; Yang, Chun-Ming; Helberg, Julian; Mayer, Peter; Marek, Ilan; Knochel, Paul Highly diastereoselective preparation of aldol products using new functionalized allylic aluminum reagents. Organic letters, 2014, 16, 956-959 |
1513479 | CIF | C31 H34 O3 | P -1 | 9.904; 10.686; 12.143 107.112; 97.167; 94.954 | 1208.3 | Nagamoto, Yuuki; Yamaoka, Yousuke; Fujimura, Shun; Takemoto, Yoshiji; Takasu, Kiyosei Synthesis of Functionalized Polycyclic Aromatic Compounds via a Formal [2 + 2]-Cycloaddition. Organic letters, 2014, 16, 1008-1011 |
1513480 | CIF | C30 H30 O2 | P -1 | 4.8479; 14.348; 16.644 87.138; 81.679; 80.307 | 1128.8 | Nagamoto, Yuuki; Yamaoka, Yousuke; Fujimura, Shun; Takemoto, Yoshiji; Takasu, Kiyosei Synthesis of Functionalized Polycyclic Aromatic Compounds via a Formal [2 + 2]-Cycloaddition. Organic letters, 2014, 16, 1008-1011 |
1513481 | CIF | C13 H14 O4 | C 1 2 1 | 21.8649; 13.0933; 17.7804 90; 110.708; 90 | 4761.4 | Youn, So Won; Song, Hyoung Sub; Park, Jong Hyub Asymmetric Domino Multicatalysis for the Synthesis of 3-Substituted Phthalides: Cinchonine/NHC Cooperative System. Organic letters, 2014, 16, 1028-1031 |
1513482 | CIF | C21 H21 Br N2 O4 | P 1 21 1 | 10.0332; 8.471; 12.9591 90; 107.322; 90 | 1051.46 | Weng, Jian-Quan; Deng, Qiao-Man; Wu, Liang; Xu, Kai; Wu, Hao; Liu, Ren-Rong; Gao, Jian-Rong; Jia, Yi-Xia Asymmetric Friedel-Crafts Alkylation of α-Substituted β-Nitroacrylates: Access to β(2,2)-Amino Acids Bearing Indolic All-Carbon Quaternary Stereocenters Organic Letters, 2014, 16, 776-779 |
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