Crystallography Open Database
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Searching journal of publication like 'Organic letters' volume of publication is 17
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
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1555389 | CIF | C29 H25 Br N2 O3 | P b c a | 12.7295; 15.5318; 24.571 90; 90; 90 | 4858 | Li, Falin; Chen, Jiangfei; Hou, Yading; Li, Yujie; Wu, Xin-Yan; Tong, Xiaofeng 1,3-Dipolar Cycloadditions of 4-Acetoxy Allenoates: Access to 2,3-Dihydropyrazoles, 2,3-Dihydroisoxazoles, and Indolizines. Organic letters, 2015, 17, 5376-5379 |
1555390 | CIF | C23 H25 N S2 | P 1 21/c 1 | 7.4977; 11.606; 23.037 90; 91.639; 90 | 2003.8 | Yamauchi, Takayuki; Shibahara, Fumitoshi; Murai, Toshiaki Direct C-H Bond Arylation of Thienyl Thioamides Catalyzed by Pd-Phenanthroline Complexes. Organic letters, 2015, 17, 5392-5395 |
1555391 | CIF | C48 H70 Cl I2 N7 O | P 21 21 21 | 11.7863; 15.6266; 27.3025 90; 90; 90 | 5028.57 | Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S. Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors. Organic letters, 2015, 17, 5740-5743 |
1555392 | CIF | C54.5 H73 Cl5 I2 N8 | P n m a | 16.4441; 19.3772; 19.7044 90; 90; 90 | 6278.62 | Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S. Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors. Organic letters, 2015, 17, 5740-5743 |
1555393 | CIF | C37 H35 I2 N7 | C 1 2/c 1 | 50.2116; 8.9517; 25.5239 90; 111.754; 90 | 10655.4 | Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S. Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors. Organic letters, 2015, 17, 5740-5743 |
1555394 | CIF | C91 H108 Cl3 I4 N15 O4 | P 1 21/c 1 | 20.9995; 15.2694; 28.6315 90; 90.725; 90 | 9179.9 | Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S. Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors. Organic letters, 2015, 17, 5740-5743 |
1555395 | CIF | C37 H35 I2 N7 O2 | P 1 21/c 1 | 17.3106; 15.673; 15.0038 90; 109.469; 90 | 3837.91 | Tepper, Ronny; Schulze, Benjamin; Görls, Helmar; Bellstedt, Peter; Jäger, Michael; Schubert, Ulrich S. Preorganization in a Cleft-Type Anion Receptor Featuring Iodo-1,2,3-Triazoles As Halogen Bond Donors. Organic letters, 2015, 17, 5740-5743 |
1555396 | CIF | C13 H20 N2 O7 | P 21 21 21 | 7.5247; 13.1309; 15.066 90; 90; 90 | 1488.61 | Habibian, Maryam; Martínez-Montero, Saúl; Portella, Guillem; Chua, Zhijie; Bohle, D. Scott; Orozco, Modesto; Damha, Masad J. Seven-Membered Ring Nucleoside Analogues: Stereoselective Synthesis and Studies on Their Conformational Properties. Organic letters, 2015, 17, 5416-5419 |
1555397 | CIF | C62 H73.33 N13 O12 | R -3 :H | 20.9278; 20.9278; 11.7428 90; 90; 120 | 4454 | Ren, Changliang; Shen, Jie; Zeng, Huaqiang One-Pot Synthesis of Strained Macrocyclic Pyridone Hexamers and Their High Selectivity toward Cu(2+) Recognition. Organic letters, 2015, 17, 5946-5949 |
1555398 | CIF | C19 H26 O2 | P 1 21 1 | 7.2207; 10.6225; 10.6751 90; 101.193; 90 | 803.23 | Weber, Manuel; Owens, Kyle; Masarwa, Ahmad; Sarpong, Richmond Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction. Organic letters, 2015, 17, 5432-5435 |
1555399 | CIF | C18 H22 O3 | P 21 21 21 | 7.5988; 8.4424; 21.953 90; 90; 90 | 1408.33 | Weber, Manuel; Owens, Kyle; Masarwa, Ahmad; Sarpong, Richmond Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction. Organic letters, 2015, 17, 5432-5435 |
1555400 | CIF | C20 H23 N O3 | P 21 21 21 | 7.2672; 12.3762; 18.5597 90; 90; 90 | 1669.27 | Weber, Manuel; Owens, Kyle; Masarwa, Ahmad; Sarpong, Richmond Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction. Organic letters, 2015, 17, 5432-5435 |
1555401 | CIF | C19 H23 N O2 | P 1 21 1 | 7.5354; 8.5029; 11.9989 90; 90.259; 90 | 768.79 | Weber, Manuel; Owens, Kyle; Masarwa, Ahmad; Sarpong, Richmond Construction of Enantiopure Taxoid and Natural Product-like Scaffolds Using a C-C Bond Cleavage/Arylation Reaction. Organic letters, 2015, 17, 5432-5435 |
1555402 | CIF | C22 H15 Cl O | P -1 | 6.5461; 8.998; 14.2101 92.224; 101.253; 92.809 | 818.92 | Arunprasath, Dhanarajan; Muthupandi, Pandi; Sekar, Govindasamy Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones. Organic letters, 2015, 17, 5448-5451 |
1555403 | CIF | C22 H15 Br O | P 1 21/c 1 | 6.253; 15.418; 17.593 90; 92.18; 90 | 1694.9 | Arunprasath, Dhanarajan; Muthupandi, Pandi; Sekar, Govindasamy Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones. Organic letters, 2015, 17, 5448-5451 |
1555404 | CIF | C22 H16 O | P 1 21/c 1 | 16.0902; 5.6098; 17.2424 90; 94.43; 90 | 1551.7 | Arunprasath, Dhanarajan; Muthupandi, Pandi; Sekar, Govindasamy Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones. Organic letters, 2015, 17, 5448-5451 |
1555405 | CIF | C23 H22 Cl N O4 | P 21 21 2 | 25.273; 6.4369; 12.9596 90; 90; 90 | 2108.3 | Liu, Hua-Chao; Liu, Kang; Xue, Zhi-Yong; He, Zhao-Lin; Wang, Chun-Jiang Silver(I)-Catalyzed Enantioselective Desymmetrization of Cyclopentenediones: Access to Highly Functionalized Bicyclic Pyrrolidines. Organic letters, 2015, 17, 5440-5443 |
1555406 | CIF | C17 H15 N O6 S | P 1 21 1 | 7.5529; 11.091; 10.123 90; 104.11; 90 | 822.4 | Li, Zequan; Shi, Yian Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds. Organic letters, 2015, 17, 5752-5755 |
1555407 | CIF | C24 H21 N O6 S | P 21 21 21 | 7.7963; 11.5859; 23.086 90; 90; 90 | 2085.3 | Li, Zequan; Shi, Yian Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds. Organic letters, 2015, 17, 5752-5755 |
1555408 | CIF | C18 H15 Br2 Cl2 N O5 S | P 1 21 1 | 11.974; 5.7044; 15.451 90; 95.49; 90 | 1050.5 | Li, Zequan; Shi, Yian Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds. Organic letters, 2015, 17, 5752-5755 |
1555409 | CIF | C20 H19 N O5 S | P 21 21 21 | 7.7017; 8.4118; 27.288 90; 90; 90 | 1767.9 | Li, Zequan; Shi, Yian Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds. Organic letters, 2015, 17, 5752-5755 |
1555410 | CIF | C17 H14 N4 O5 S | P 1 21 1 | 8.3457; 10.924; 9.879 90; 109.46; 90 | 849.2 | Li, Zequan; Shi, Yian Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds. Organic letters, 2015, 17, 5752-5755 |
1555411 | CIF | C17 H14 Br N O5 S | P 1 21 1 | 8.091; 6.973; 15.224 90; 101.811; 90 | 840.7 | Li, Zequan; Shi, Yian Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds. Organic letters, 2015, 17, 5752-5755 |
1555412 | CIF | C17 H12 Br F2 N O5 S | P 21 21 21 | 6.8957; 12.551; 22.629 90; 90; 90 | 1958.5 | Li, Zequan; Shi, Yian Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds. Organic letters, 2015, 17, 5752-5755 |
1555413 | CIF | C21 H17 N O5 S2 | C 2 2 21 | 11.289; 10.612; 32.425 90; 90; 90 | 3884.5 | Li, Zequan; Shi, Yian Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds. Organic letters, 2015, 17, 5752-5755 |
1555414 | CIF | C19 H17 Br Cl N O5 S | P 21 21 21 | 9.155; 9.47; 23.095 90; 90; 90 | 2002.3 | Li, Zequan; Shi, Yian Chiral Phosphine Oxide-Sc(OTf)3 Complex Catalyzed Enantioselective Bromoaminocyclization of 2-Benzofuranylmethyl N-Tosylcarbamates. Approach to a Novel Class of Optically Active Spiro Compounds. Organic letters, 2015, 17, 5752-5755 |
1555415 | CIF | C14 H22 O4 | P 21 21 21 | 6.5953; 9.079; 21.403 90; 90; 90 | 1281.6 | Shen, Yang; Li, Linbin; Pan, Zhisheng; Wang, Yinglu; Li, Jundong; Wang, Kuangyu; Wang, Xiance; Zhang, Youyu; Hu, Tianhui; Zhang, Yandong Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans. Organic letters, 2015, 17, 5480-5483 |
1555416 | CIF | C18 H28 O4 Si | P 21 21 21 | 7.2691; 11.4811; 21.668 90; 90; 90 | 1808.4 | Shen, Yang; Li, Linbin; Pan, Zhisheng; Wang, Yinglu; Li, Jundong; Wang, Kuangyu; Wang, Xiance; Zhang, Youyu; Hu, Tianhui; Zhang, Yandong Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans. Organic letters, 2015, 17, 5480-5483 |
1555417 | CIF | C15 H18 O7 | P 1 21 1 | 7.187; 8.7702; 11.015 90; 98.176; 90 | 687.23 | Shen, Yang; Li, Linbin; Pan, Zhisheng; Wang, Yinglu; Li, Jundong; Wang, Kuangyu; Wang, Xiance; Zhang, Youyu; Hu, Tianhui; Zhang, Yandong Protecting-Group-Free Total Synthesis of (-)-Jiadifenolide: Development of a [4 + 1] Annulation toward Multisubstituted Tetrahydrofurans. Organic letters, 2015, 17, 5480-5483 |
1555418 | CIF | C17 H16 F6 O9 | P 1 21/c 1 | 13.5602; 8.6298; 17.3709 90; 92.1; 90 | 2031.4 | Nakhla, Mina C.; Lee, Che-Wah; Wood, John L. Chemoselective Intramolecular Carbonyl Ylide Formation through Electronically Differentiated Malonate Diesters. Organic letters, 2015, 17, 5760-5763 |
1555419 | CIF | C11 H17 O5 | P 1 21/n 1 | 6.4697; 11.6627; 16.0124 90; 93.278; 90 | 1206.23 | Nakhla, Mina C.; Lee, Che-Wah; Wood, John L. Chemoselective Intramolecular Carbonyl Ylide Formation through Electronically Differentiated Malonate Diesters. Organic letters, 2015, 17, 5760-5763 |
1555420 | CIF | C17 H19 F3 O9 | P 1 21/c 1 | 13.9325; 8.4366; 16.9502 90; 92.536; 90 | 1990.4 | Nakhla, Mina C.; Lee, Che-Wah; Wood, John L. Chemoselective Intramolecular Carbonyl Ylide Formation through Electronically Differentiated Malonate Diesters. Organic letters, 2015, 17, 5760-5763 |
1555421 | CIF | C24 H31 N O5 S | P 21 21 21 | 5.8376; 10.6992; 37.5454 90; 90; 90 | 2345 | Serpier, Fabien; Brayer, Jean-Louis; Folléas, Benoît; Darses, Sylvain Access to Polyfunctionalized Chiral Piperidines through Enantioselective Addition-Carbocyclization Cascade Reaction Catalyzed by a Rhodium(I)-Diene Complex. Organic letters, 2015, 17, 5496-5499 |
1555422 | CIF | C16 H18 Li N2 O | P b c n | 15.9311; 9.7436; 9.2498 90; 90; 90 | 1435.81 | Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A. Interaction of Azobenzene and Benzalaniline with Strong Amido Bases. Organic letters, 2015, 17, 6154-6157 |
1555423 | CIF | C28 H32 N2 Si2 | P 1 21/c 1 | 8.4866; 18.1483; 16.7017 90; 97.928; 90 | 2547.8 | Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A. Interaction of Azobenzene and Benzalaniline with Strong Amido Bases. Organic letters, 2015, 17, 6154-6157 |
1555424 | CIF | C44 H62 Li2 N4 O2 | C 1 2/c 1 | 26.34; 11.0689; 18.748 90; 134.32; 90 | 3910.7 | Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A. Interaction of Azobenzene and Benzalaniline with Strong Amido Bases. Organic letters, 2015, 17, 6154-6157 |
1555425 | CIF | C39 H46 N2 Si2 | P c a 21 | 13.9869; 12.5966; 19.4789 90; 90; 90 | 3431.9 | Kornev, Alexander N.; Sushev, Vyacheslav V.; Zolotareva, Natalia V.; Baranov, Evgenii V.; Fukin, Georgy K.; Abakumov, Gleb A. Interaction of Azobenzene and Benzalaniline with Strong Amido Bases. Organic letters, 2015, 17, 6154-6157 |
1555426 | CIF | C13 H15 B F N O5 | P 1 21/c 1 | 13.4038; 9.8242; 11.011 90; 110.376; 90 | 1359.2 | St Denis, Jeffrey D.; Lee, C. Frank; Yudin, Andrei K. Access to Cyclic Amino Boronates via Rhodium-Catalyzed Functionalization of Alkyl MIDA Boronates. Organic letters, 2015, 17, 5764-5767 |
1555427 | CIF | C15.5 H20 B N2 O7.5 S | P 1 21/c 1 | 10.3226; 15.7804; 11.1047 90; 107.792; 90 | 1722.38 | St Denis, Jeffrey D.; Lee, C. Frank; Yudin, Andrei K. Access to Cyclic Amino Boronates via Rhodium-Catalyzed Functionalization of Alkyl MIDA Boronates. Organic letters, 2015, 17, 5764-5767 |
1555428 | CIF | C15 H12 Cl2 O S2 | P n m a | 6.9371; 9.8082; 22.3442 90; 90; 90 | 1520.31 | Huang, Xin; Wang, Jichao; Ni, Zhangqin; Wang, Sichang; Pan, Yuanjiang Synthesis of α,α-Disulfenylated Aldehydes via Oxidative Transformation of Tertiary Amines. Organic letters, 2015, 17, 5488-5491 |
1555429 | CIF | C82 H54 N4 | P -1 | 10.1789; 11.9937; 13.2135 108.6; 95.189; 102.354 | 1471.38 | Liu, Yulong; Shan, Tong; Yao, Liang; Bai, Qing; Guo, Yachen; Li, Jinyu; Han, Xiao; Li, Weijun; Wang, Zhiming; Yang, Bing; Lu, Ping; Ma, Yuguang Isomers of Pyrene-Imidazole Compounds: Synthesis and Configuration Effect on Optical Properties. Organic letters, 2015, 17, 6138-6141 |
1555430 | CIF | C82 H54 N4 | P -1 | 10.0347; 11.9855; 25.329 77.339; 87.855; 87.767 | 2968.7 | Liu, Yulong; Shan, Tong; Yao, Liang; Bai, Qing; Guo, Yachen; Li, Jinyu; Han, Xiao; Li, Weijun; Wang, Zhiming; Yang, Bing; Lu, Ping; Ma, Yuguang Isomers of Pyrene-Imidazole Compounds: Synthesis and Configuration Effect on Optical Properties. Organic letters, 2015, 17, 6138-6141 |
1555431 | CIF | C20 H15 Cl N2 O5 | P 1 21 1 | 12.275; 11.187; 13.371 90; 104.835; 90 | 1774.9 | Gao, Hang; Luo, Zhenli; Ge, Pingjin; He, Junqian; Zhou, Feng; Zheng, Peipei; Jiang, Jun Direct Catalytic Asymmetric Synthesis of β-Hydroxy Acids from Malonic Acid. Organic letters, 2015, 17, 5962-5965 |
1555432 | CIF | C25.5 H31 Cl1.5 N2 O5 P S | P 1 21 1 | 13.5437; 13.0346; 16.0277 90; 102.411; 90 | 2763.4 | Kayal, Satavisha; Mukherjee, Santanu Catalytic Aldol-Cyclization Cascade of 3-Isothiocyanato Oxindoles with α-Ketophosphonates for the Enantioselective Synthesis of β-Amino-α-hydroxyphosphonates. Organic letters, 2015, 17, 5508-5511 |
1555433 | CIF | C19 H18 F3 N O2 S | P 1 c 1 | 8.9711; 9.9056; 10.1296 90; 94.135; 90 | 897.8 | Zhu, Zi-Zhong; Chen, Kai; Yu, Liu-Zhu; Tang, Xiang-Ying; Shi, Min Copper(I)-Catalyzed Intramolecular Trifluoromethylation of Methylenecyclopropanes. Organic letters, 2015, 17, 5994-5997 |
1555434 | CIF | C40 H20 O3 | P 1 21/c 1 | 7.63737; 22.5914; 15.1095 90; 99.906; 90 | 2568.11 | Shyam Sundar, M.; Bedekar, Ashutosh V. Synthesis and Study of 7,12,17-Trioxa[11]helicene. Organic letters, 2015, 17, 5808-5811 |
1555435 | CIF | C22 H16 O4 | P n a 21 | 23.0883; 8.2485; 17.6035 90; 90; 90 | 3352.5 | Shyam Sundar, M.; Bedekar, Ashutosh V. Synthesis and Study of 7,12,17-Trioxa[11]helicene. Organic letters, 2015, 17, 5808-5811 |
1555436 | CIF | C24 H24 N4 O3 | C 1 2 1 | 37.9789; 14.5891; 21.4715 90; 119.848; 90 | 10318.8 | Yang, Van-Wei; Hong, Bor-Cherng; Kao, Hsin-Kai; Tu, Ting-Hsun; Shen, Jiun-Yi; Chen, Chi-Lin; Lee, Gene-Hsiang; Chou, Pi-Tai One-Pot Dichotomous Construction of Inside-Azayohimban and Pro-Azayohimban Systems via an Enantioselective Organocatalytic Cascade; Their Use as a Model to Probe the (Aza-)Indole Local Solvent Environment. Organic letters, 2015, 17, 5816-5819 |
1555437 | CIF | C25 H28 N4 O5 | P 21 21 21 | 8.2785; 9.2956; 29.7576 90; 90; 90 | 2289.96 | Yang, Van-Wei; Hong, Bor-Cherng; Kao, Hsin-Kai; Tu, Ting-Hsun; Shen, Jiun-Yi; Chen, Chi-Lin; Lee, Gene-Hsiang; Chou, Pi-Tai One-Pot Dichotomous Construction of Inside-Azayohimban and Pro-Azayohimban Systems via an Enantioselective Organocatalytic Cascade; Their Use as a Model to Probe the (Aza-)Indole Local Solvent Environment. Organic letters, 2015, 17, 5816-5819 |
1555438 | CIF | C44 H63 N5 O11 | P 1 21/c 1 | 19.5349; 6.5541; 34.67 90; 95.943; 90 | 4415.1 | Tabor, M. Greg; Shenvi, Ryan A. Synthesis of Lepadiformine Using a Hydroamination Transform. Organic letters, 2015, 17, 5776-5779 |
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