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 |
|---|---|---|---|---|---|---|
| 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 |
| 1555439 | CIF | C15 H15 N O | P 1 21 1 | 7.0716; 6.6011; 13.3983 90; 92.659; 90 | 624.76 | Vita, Maria Victoria; Caramenti, Paola; Waser, Jerome Enantioselective Synthesis of Homoallylic Azides and Nitriles via Palladium-Catalyzed Decarboxylative Allylation. Organic letters, 2015, 17, 5832-5835 |
| 1555440 | CIF | C29 H30 Br N3 O | P -1 | 8.9762; 9.2143; 15.8055 91.311; 97.75; 93.388 | 1292.4 | Duan, Xiao-Yong; Yang, Xiu-Long; Jia, Pan-Pan; Zhang, Man; Han, Bing Hydrazonyl Radical-Participated Tandem Reaction: A Strategy for the Synthesis of Pyrazoline-Functionalized Oxindoles. Organic letters, 2015, 17, 6022-6025 |
| 1555441 | CIF | C18 H13 N O3 | P 1 21/n 1 | 9.2686; 16.156; 9.4109 90; 95.246; 90 | 1403.3 | Sengoku, Tetsuya; Murata, Yusuke; Aso, Yuwa; Kawakami, Ai; Inuzuka, Toshiyasu; Sakamoto, Masami; Takahashi, Masaki; Yoda, Hidemi Indium-Catalyzed Amide Allylation of N-Carbonyl Imides: Formation of Azaspiro-γ-lactones via Ring Opening-Reclosure. Organic letters, 2015, 17, 5846-5849 |
| 1555442 | CIF | C104 H170 Cl8 Cu2 N16 O17 | C 1 2/c 1 | 25.299; 19.2324; 28.254 90; 91.806; 90 | 13740 | Ganss, Alexander; Belda, Raquel; Pitarch, Javier; Goddard, Richard; García-España, Enrique; Kubik, Stefan Synthesis and Structural Characterization of a Cyclen-Derived Molecular Cage. Organic letters, 2015, 17, 5850-5853 |
| 1555443 | CIF | C28 H32 Br N3 O3 | P 1 21/c 1 | 16.0245; 8.5681; 19.233 90; 95.076; 90 | 2630.3 | Douchez, Antoine; Lubell, William D. Chemoselective Alkylation for Diversity-Oriented Synthesis of 1,3,4-Benzotriazepin-2-ones and Pyrrolo[1,2][1,3,4]benzotriazepin-6-ones, Potential Turn Surrogates. Organic letters, 2015, 17, 6046-6049 |
| 1555444 | CIF | C20 H15 Br Cl N3 O3 | P 1 21/n 1 | 8.8959; 13.3302; 15.9639 90; 91.132; 90 | 1892.7 | Douchez, Antoine; Lubell, William D. Chemoselective Alkylation for Diversity-Oriented Synthesis of 1,3,4-Benzotriazepin-2-ones and Pyrrolo[1,2][1,3,4]benzotriazepin-6-ones, Potential Turn Surrogates. Organic letters, 2015, 17, 6046-6049 |
| 1555445 | CIF | C24 H21 N5 O2 | P -1 | 8.7322; 9.9954; 12.0561 78.166; 89.574; 82.698 | 1021.37 | Ramanathan, Mani; Wang, Yu-Hao; Liu, Shiuh-Tzung One-Pot Reactions for Synthesis of 2,5-Substituted Tetrazoles from Aryldiazonium Salts and Amidines. Organic letters, 2015, 17, 5886-5889 |
| 1555446 | CIF | C18 H22 O2 | P 21 21 21 | 9.0068; 10.478; 16.4734 90; 90; 90 | 1554.65 | Lai, Zengwei; Wang, Zhaobin; Sun, Jianwei Organocatalytic Asymmetric Nucleophilic Addition to o-Quinone Methides by Alcohols. Organic letters, 2015, 17, 6058-6061 |
| 1555447 | CIF | C21 H16 O3 | P b c a | 15.108; 7.54; 27.9119 90; 90; 90 | 3179.6 | Ravi Kumar, Devarapalli; Satyanarayana, Gedu Domino Oxidative [Pd]-Catalysis: One-Pot Synthesis of Fluorenones Starting from Simple Benzylamines and Iodo Arenes. Organic letters, 2015, 17, 5894-5897 |
| 1555448 | CIF | C15 H12 O3 | P 1 21/n 1 | 7.8593; 4.0079; 36.679 90; 93.567; 90 | 1153.1 | Ravi Kumar, Devarapalli; Satyanarayana, Gedu Domino Oxidative [Pd]-Catalysis: One-Pot Synthesis of Fluorenones Starting from Simple Benzylamines and Iodo Arenes. Organic letters, 2015, 17, 5894-5897 |
| 1555449 | CIF | C20 H30 O2 | C 1 2 1 | 20.0748; 6.8584; 25.9078 90; 106.399; 90 | 3421.9 | Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization. Organic letters, 2015, 17, 6062-6065 |
| 1555450 | CIF | C24 H36 O4 | P 1 21 1 | 11.623; 7.3026; 12.673 90; 95.271; 90 | 1071.1 | Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization. Organic letters, 2015, 17, 6062-6065 |
| 1555451 | CIF | C24 H36 O4 | C 1 2 1 | 31.775; 7.261; 19.184 90; 104.026; 90 | 4294.1 | Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization. Organic letters, 2015, 17, 6062-6065 |
| 1555452 | CIF | C24 H36 O4 | P 1 21 1 | 10.27; 7.257; 14.424 90; 92.479; 90 | 1074 | Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization. Organic letters, 2015, 17, 6062-6065 |
| 1555453 | CIF | C38 H54 O5 | P 21 21 21 | 10.0955; 13.4185; 24.927 90; 90; 90 | 3376.8 | Zhou, Min; Li, Xing-Ren; Tang, Jian-Wei; Liu, Yang; Li, Xiao-Nian; Wu, Bin; Qin, Hong-Bo; Du, Xue; Li, Li-Mei; Wang, Wei-Guang; Pu, Jian-Xin; Sun, Han-Dong Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C-H Functionalization. Organic letters, 2015, 17, 6062-6065 |
| 1555454 | CIF | C62 H84 N8 O2 S2 Si4 | P -1 | 8.2413; 12.7682; 15.6926 80.64; 82.824; 75.922 | 1574.06 | Cortizo-Lacalle, Diego; Gozalvez, Cristian; Olano, Mikel; Sun, Xiangnan; Melle-Franco, Manuel; Hueso, Luis E.; Mateo-Alonso, Aurelio Bisthiadiazole-Fused Tetraazapentacenequinone: An Air-Stable Solution-Processable n-Type Organic Semiconductor. Organic letters, 2015, 17, 5902-5905 |
| 1555455 | CIF | C31 H23 Cl2 N O4 S | P -1 | 9.8014; 12.1207; 13.323 99.552; 106.402; 111.742 | 1343.8 | Zhu, Yi-Long; Jiang, Bo; Hao, Wen-Juan; Qiu, Jiang-Kai; Sun, Jun; Wang, De-Cai; Wei, Ping; Wang, Ai-Fang; Li, Guigen; Tu, Shu-Jiang Catalytic Arylsulfonyl Radical Triggered 1,7-Enyne Bicyclizations. Organic letters, 2015, 17, 6078-6081 |
| 1555456 | CIF | C30 H21 Cl2 N O3 S | P -1 | 7.3264; 7.7051; 23.332 84.594; 88.837; 82.404 | 1299.7 | Zhu, Yi-Long; Jiang, Bo; Hao, Wen-Juan; Qiu, Jiang-Kai; Sun, Jun; Wang, De-Cai; Wei, Ping; Wang, Ai-Fang; Li, Guigen; Tu, Shu-Jiang Catalytic Arylsulfonyl Radical Triggered 1,7-Enyne Bicyclizations. Organic letters, 2015, 17, 6078-6081 |
| 1555457 | CIF | C23 H18 N2 O3 S | P -1 | 9.5468; 10.4076; 11.3179 103.653; 93.612; 114.414 | 978.53 | Qiao, Huijie; Sun, Suyan; Yang, Fan; Zhu, Yu; Zhu, Weiguo; Dong, Yaxi; Wu, Yusheng; Kong, Xiangtao; Jiang, Ling; Wu, Yangjie Copper(I)-Catalyzed Sulfonylation of 8-Aminoquinoline Amides with Sulfonyl Chlorides in Air. Organic letters, 2015, 17, 6086-6089 |
| 1555458 | CIF | C56 H40 F6 N6 | P 1 21/c 1 | 7.398; 11.831; 25.874 90; 94.823; 90 | 2256.6 | Tasior, Mariusz; Chotkowski, Maciej; Gryko, Daniel T. Extension of Pyrrolopyrrole π-System: Approach to Constructing Hexacyclic Nitrogen-Containing Aromatic Systems. Organic letters, 2015, 17, 6106-6109 |
| 1555459 | CIF | C136 H112 O | P -1 | 10.6194; 15.7603; 16.3359 73.944; 87.761; 73.938 | 2522.8 | He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes. Organic letters, 2015, 17, 6174-6177 |
| 1555460 | CIF | C62.74 H45.48 Cl1.48 | P -1 | 9.9913; 15.4197; 15.7043 102.428; 92.308; 99.776 | 2321 | He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes. Organic letters, 2015, 17, 6174-6177 |
| 1555461 | CIF | C104 H80 O | P -1 | 10.2023; 12.2529; 16.1191 98.99; 102.37; 105.55 | 1846.7 | He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes. Organic letters, 2015, 17, 6174-6177 |
| 1555462 | CIF | C52 H40 O0.5 | P -1 | 10.11; 10.19; 36.97 91.2; 94.1; 95.6 | 3779.3 | He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes. Organic letters, 2015, 17, 6174-6177 |
| 1555463 | CIF | C58 H52 O | C 1 2/c 1 | 30.72; 17.174; 16.373 90; 97.824; 90 | 8557.7 | He, Bairong; Nie, Han; Chen, Long; Lou, Xiaoding; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong High Fluorescence Efficiencies and Large Stokes Shifts of Folded Fluorophores Consisting of a Pair of Alkenyl-Tethered, π-Stacked Oligo-p-phenylenes. Organic letters, 2015, 17, 6174-6177 |
| 1555464 | CIF | C19 H17 Cl N2 O1.425 | P 1 21/c 1 | 13.0804; 18.104; 15.8995 90; 102.512; 90 | 3675.7 | Jiang, Pingping; Li, Feng; Xu, Yongbao; Liu, Qingwen; Wang, Jing; Ding, Hong; Yu, Renfu; Wang, Qifeng Aromaticity-Dependent Regioselectivity in Pd(II)-Catalyzed C-H Direct Arylation of Aryl Ureas. Organic letters, 2015, 17, 5918-5921 |
| 1555465 | CIF | C21 H14 O4 | P n a 21 | 9.2786; 23.641; 7.5289 90; 90; 90 | 1651.5 | Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols. Organic letters, 2015, 17, 5926-5929 |
| 1555466 | CIF | C15 H12 O3 | P 1 21/n 1 | 13.899; 6.5834; 14.579 90; 117.751; 90 | 1180.6 | Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols. Organic letters, 2015, 17, 5926-5929 |
| 1555467 | CIF | C20 H14 O2 | P 21 21 21 | 7.3238; 9.814; 19.747 90; 90; 90 | 1419.3 | Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols. Organic letters, 2015, 17, 5926-5929 |
| 1555468 | CIF | C14 H10 O3 | P 1 21/n 1 | 10.271; 9.1771; 11.2051 90; 97.686; 90 | 1046.7 | Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols. Organic letters, 2015, 17, 5926-5929 |
| 1555469 | CIF | C22 H14 O3 | P b c a | 12.5409; 7.8473; 31.588 90; 90; 90 | 3108.6 | Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols. Organic letters, 2015, 17, 5926-5929 |
| 1555470 | CIF | C19 H14 O3 | P -1 | 6.866; 10.24; 11.188 69.311; 72.734; 83.093 | 702.6 | Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols. Organic letters, 2015, 17, 5926-5929 |
| 1555471 | CIF | C17 H13 N O3 | P 1 21/c 1 | 4.629; 16.421; 17.474 90; 91.158; 90 | 1328 | Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols. Organic letters, 2015, 17, 5926-5929 |
| 1555472 | CIF | C18 H12 O3 | P -1 | 7.4224; 7.787; 12.133 99.775; 91.453; 97.925 | 683.6 | Zhao, Jidong; Liu, Jun; Xie, Xin; Li, Shi; Liu, Yuanhong Gold-Catalyzed Synthesis of Tropone and Its Analogues via Oxidative Ring Expansion of Alkynyl Quinols. Organic letters, 2015, 17, 5926-5929 |
| 1555473 | CIF | C21 H19 N O5 | P 1 21/c 1 | 9.3725; 21.712; 9.3146 90; 106.094; 90 | 1821.2 | Hong, Jung-Ho; Atta, Ananta Kumar; Jung, Kwang-Bok; Kim, Seul-Bi; Heo, Jungseok; Cho, Dong-Gyu Conformationally Locked Tolans, β-Sheet Structures, and Photophysical Properties. Organic letters, 2015, 17, 6222-6225 |
| 1555474 | CIF | C17 H22 N O3 S | P 1 21 1 | 8.5345; 8.8037; 11.0062 90; 90.369; 90 | 826.94 | Moynihan, Lorna; Chadda, Rekha; McArdle, Patrick; Murphy, Paul V. Allylic Azide Rearrangement in Tandem with Huisgen Cycloaddition for Stereoselective Annulation: Synthesis of C-Glycosyl Iminosugars. Organic letters, 2015, 17, 6226-6229 |
| 1555475 | CIF | C13 H18 N3 O4 | P 1 21 1 | 6.1187; 15.5628; 7.4298 90; 90.617; 90 | 707.46 | Moynihan, Lorna; Chadda, Rekha; McArdle, Patrick; Murphy, Paul V. Allylic Azide Rearrangement in Tandem with Huisgen Cycloaddition for Stereoselective Annulation: Synthesis of C-Glycosyl Iminosugars. Organic letters, 2015, 17, 6226-6229 |
| 1555476 | CIF | C10 H20 O S2 Si | P 1 21 1 | 6.642; 14.2879; 13.6807 90; 91.605; 90 | 1297.79 | Melillo, Bruno; Chen, Ming Z.; Forestieri, Roberto; Smith, 3rd, Amos B An Effective Bifunctional Aldehyde Linchpin for Type II Anion Relay Chemistry: Development and Application to the Synthesis of a C16-C29 Fragment of Rhizopodin. Organic letters, 2015, 17, 6242-6245 |
| 1555477 | CIF | C18 H34 O S4 Si | P -1 | 9.7683; 10.4783; 12.5293 102.548; 99.034; 115.038 | 1088.3 | Melillo, Bruno; Chen, Ming Z.; Forestieri, Roberto; Smith, 3rd, Amos B An Effective Bifunctional Aldehyde Linchpin for Type II Anion Relay Chemistry: Development and Application to the Synthesis of a C16-C29 Fragment of Rhizopodin. Organic letters, 2015, 17, 6242-6245 |
| 1555478 | CIF | C23 H21 N O | P 1 21/c 1 | 12.2975; 14.2131; 10.3046 90; 107.61; 90 | 1716.7 | Taguchi, Masamitsu; Tokimizu, Yusuke; Oishi, Shinya; Fujii, Nobutaka; Ohno, Hiroaki Synthesis of Fused Carbazoles by Gold-Catalyzed Tricyclization of Conjugated Diynes via Rearrangement of an N-Propargyl Group. Organic letters, 2015, 17, 6250-6253 |
| 1555480 | CIF | C21 H18 Br N | P 1 21 1 | 10.094; 14.285; 11.689 90; 90.952; 90 | 1685.2 | Zhang, Zhenhua; Du, Haifeng Enantioselective Metal-Free Hydrogenations of Disubstituted Quinolines. Organic letters, 2015, 17, 6266-6269 |
| 1555481 | CIF | C24 H24 N2 O2 | P 1 21/c 1 | 9.0073; 29.18; 7.8919 90; 104.587; 90 | 2007.39 | Bhojgude, Sachin Suresh; Baviskar, Dnyaneshwar R.; Gonnade, Rajesh G.; Biju, Akkattu T. Three-Component Coupling Involving Arynes, Aromatic Tertiary Amines, and Aldehydes via Aryl-Aryl Amino Group Migration. Organic letters, 2015, 17, 6270-6273 |
| 1555482 | CIF | C24 H24 N2 O | P -1 | 10.369; 13.94; 14.494 83.533; 85.279; 75.051 | 2008.1 | Bhojgude, Sachin Suresh; Baviskar, Dnyaneshwar R.; Gonnade, Rajesh G.; Biju, Akkattu T. Three-Component Coupling Involving Arynes, Aromatic Tertiary Amines, and Aldehydes via Aryl-Aryl Amino Group Migration. Organic letters, 2015, 17, 6270-6273 |
| 1555483 | CIF | C25 H30 N2 O5 | P 1 21 1 | 8.73; 13.8357; 9.1173 90; 93.75; 90 | 1098.88 | Zhang, Hua; Zhu, Kong-Kai; Han, Ying-Shan; Luo, Cheng; Wainberg, Mark A.; Yue, Jian-Min Flueggether A and Virosinine A, Anti-HIV Alkaloids from Flueggea virosa. Organic letters, 2015, 17, 6274-6277 |
| 1556257 | CIF | C17 H12 N2 O4 | P 1 21/c 1 | 13.389; 7.794; 13.881 90; 90.579; 90 | 1448.5 | Gao, Qinghe; Zhang, Jingjing; Wu, Xia; Liu, Shan; Wu, Anxin Direct regioselective oxidative cross-coupling of indoles with methyl ketones: a novel route to C3-dicarbonylation of indoles. Organic letters, 2015, 17, 134-137 |
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