Crystallography Open Database

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1555389 CIFC29 H25 Br N2 O3P b c a12.7295; 15.5318; 24.571
90; 90; 90
4858Li, 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 CIFC23 H25 N S2P 1 21/c 17.4977; 11.606; 23.037
90; 91.639; 90
2003.8Yamauchi, 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 CIFC48 H70 Cl I2 N7 OP 21 21 2111.7863; 15.6266; 27.3025
90; 90; 90
5028.57Tepper, 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 CIFC54.5 H73 Cl5 I2 N8P n m a16.4441; 19.3772; 19.7044
90; 90; 90
6278.62Tepper, 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 CIFC37 H35 I2 N7C 1 2/c 150.2116; 8.9517; 25.5239
90; 111.754; 90
10655.4Tepper, 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 CIFC91 H108 Cl3 I4 N15 O4P 1 21/c 120.9995; 15.2694; 28.6315
90; 90.725; 90
9179.9Tepper, 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 CIFC37 H35 I2 N7 O2P 1 21/c 117.3106; 15.673; 15.0038
90; 109.469; 90
3837.91Tepper, 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 CIFC13 H20 N2 O7P 21 21 217.5247; 13.1309; 15.066
90; 90; 90
1488.61Habibian, 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 CIFC62 H73.33 N13 O12R -3 :H20.9278; 20.9278; 11.7428
90; 90; 120
4454Ren, 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 CIFC19 H26 O2P 1 21 17.2207; 10.6225; 10.6751
90; 101.193; 90
803.23Weber, 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 CIFC18 H22 O3P 21 21 217.5988; 8.4424; 21.953
90; 90; 90
1408.33Weber, 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 CIFC20 H23 N O3P 21 21 217.2672; 12.3762; 18.5597
90; 90; 90
1669.27Weber, 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 CIFC19 H23 N O2P 1 21 17.5354; 8.5029; 11.9989
90; 90.259; 90
768.79Weber, 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 CIFC22 H15 Cl OP -16.5461; 8.998; 14.2101
92.224; 101.253; 92.809
818.92Arunprasath, 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 CIFC22 H15 Br OP 1 21/c 16.253; 15.418; 17.593
90; 92.18; 90
1694.9Arunprasath, 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 CIFC22 H16 OP 1 21/c 116.0902; 5.6098; 17.2424
90; 94.43; 90
1551.7Arunprasath, 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 CIFC23 H22 Cl N O4P 21 21 225.273; 6.4369; 12.9596
90; 90; 90
2108.3Liu, 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 CIFC17 H15 N O6 SP 1 21 17.5529; 11.091; 10.123
90; 104.11; 90
822.4Li, 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 CIFC24 H21 N O6 SP 21 21 217.7963; 11.5859; 23.086
90; 90; 90
2085.3Li, 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 CIFC18 H15 Br2 Cl2 N O5 SP 1 21 111.974; 5.7044; 15.451
90; 95.49; 90
1050.5Li, 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 CIFC20 H19 N O5 SP 21 21 217.7017; 8.4118; 27.288
90; 90; 90
1767.9Li, 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 CIFC17 H14 N4 O5 SP 1 21 18.3457; 10.924; 9.879
90; 109.46; 90
849.2Li, 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 CIFC17 H14 Br N O5 SP 1 21 18.091; 6.973; 15.224
90; 101.811; 90
840.7Li, 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 CIFC17 H12 Br F2 N O5 SP 21 21 216.8957; 12.551; 22.629
90; 90; 90
1958.5Li, 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 CIFC21 H17 N O5 S2C 2 2 2111.289; 10.612; 32.425
90; 90; 90
3884.5Li, 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 CIFC19 H17 Br Cl N O5 SP 21 21 219.155; 9.47; 23.095
90; 90; 90
2002.3Li, 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 CIFC14 H22 O4P 21 21 216.5953; 9.079; 21.403
90; 90; 90
1281.6Shen, 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 CIFC18 H28 O4 SiP 21 21 217.2691; 11.4811; 21.668
90; 90; 90
1808.4Shen, 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 CIFC15 H18 O7P 1 21 17.187; 8.7702; 11.015
90; 98.176; 90
687.23Shen, 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 CIFC17 H16 F6 O9P 1 21/c 113.5602; 8.6298; 17.3709
90; 92.1; 90
2031.4Nakhla, 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 CIFC11 H17 O5P 1 21/n 16.4697; 11.6627; 16.0124
90; 93.278; 90
1206.23Nakhla, 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 CIFC17 H19 F3 O9P 1 21/c 113.9325; 8.4366; 16.9502
90; 92.536; 90
1990.4Nakhla, 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 CIFC24 H31 N O5 SP 21 21 215.8376; 10.6992; 37.5454
90; 90; 90
2345Serpier, 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 CIFC16 H18 Li N2 OP b c n15.9311; 9.7436; 9.2498
90; 90; 90
1435.81Kornev, 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 CIFC28 H32 N2 Si2P 1 21/c 18.4866; 18.1483; 16.7017
90; 97.928; 90
2547.8Kornev, 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 CIFC44 H62 Li2 N4 O2C 1 2/c 126.34; 11.0689; 18.748
90; 134.32; 90
3910.7Kornev, 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 CIFC39 H46 N2 Si2P c a 2113.9869; 12.5966; 19.4789
90; 90; 90
3431.9Kornev, 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 CIFC13 H15 B F N O5P 1 21/c 113.4038; 9.8242; 11.011
90; 110.376; 90
1359.2St 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 CIFC15.5 H20 B N2 O7.5 SP 1 21/c 110.3226; 15.7804; 11.1047
90; 107.792; 90
1722.38St 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 CIFC15 H12 Cl2 O S2P n m a6.9371; 9.8082; 22.3442
90; 90; 90
1520.31Huang, 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 CIFC82 H54 N4P -110.1789; 11.9937; 13.2135
108.6; 95.189; 102.354
1471.38Liu, 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 CIFC82 H54 N4P -110.0347; 11.9855; 25.329
77.339; 87.855; 87.767
2968.7Liu, 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 CIFC20 H15 Cl N2 O5P 1 21 112.275; 11.187; 13.371
90; 104.835; 90
1774.9Gao, 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 CIFC25.5 H31 Cl1.5 N2 O5 P SP 1 21 113.5437; 13.0346; 16.0277
90; 102.411; 90
2763.4Kayal, 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 CIFC19 H18 F3 N O2 SP 1 c 18.9711; 9.9056; 10.1296
90; 94.135; 90
897.8Zhu, 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 CIFC40 H20 O3P 1 21/c 17.63737; 22.5914; 15.1095
90; 99.906; 90
2568.11Shyam Sundar, M.; Bedekar, Ashutosh V.
Synthesis and Study of 7,12,17-Trioxa[11]helicene.
Organic letters, 2015, 17, 5808-5811
1555435 CIFC22 H16 O4P n a 2123.0883; 8.2485; 17.6035
90; 90; 90
3352.5Shyam Sundar, M.; Bedekar, Ashutosh V.
Synthesis and Study of 7,12,17-Trioxa[11]helicene.
Organic letters, 2015, 17, 5808-5811
1555436 CIFC24 H24 N4 O3C 1 2 137.9789; 14.5891; 21.4715
90; 119.848; 90
10318.8Yang, 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 CIFC25 H28 N4 O5P 21 21 218.2785; 9.2956; 29.7576
90; 90; 90
2289.96Yang, 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 CIFC44 H63 N5 O11P 1 21/c 119.5349; 6.5541; 34.67
90; 95.943; 90
4415.1Tabor, M. Greg; Shenvi, Ryan A.
Synthesis of Lepadiformine Using a Hydroamination Transform.
Organic letters, 2015, 17, 5776-5779

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