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
1555439 CIFC15 H15 N OP 1 21 17.0716; 6.6011; 13.3983
90; 92.659; 90
624.76Vita, 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 CIFC29 H30 Br N3 OP -18.9762; 9.2143; 15.8055
91.311; 97.75; 93.388
1292.4Duan, 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 CIFC18 H13 N O3P 1 21/n 19.2686; 16.156; 9.4109
90; 95.246; 90
1403.3Sengoku, 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 CIFC104 H170 Cl8 Cu2 N16 O17C 1 2/c 125.299; 19.2324; 28.254
90; 91.806; 90
13740Ganss, 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 CIFC28 H32 Br N3 O3P 1 21/c 116.0245; 8.5681; 19.233
90; 95.076; 90
2630.3Douchez, 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 CIFC20 H15 Br Cl N3 O3P 1 21/n 18.8959; 13.3302; 15.9639
90; 91.132; 90
1892.7Douchez, 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 CIFC24 H21 N5 O2P -18.7322; 9.9954; 12.0561
78.166; 89.574; 82.698
1021.37Ramanathan, 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 CIFC18 H22 O2P 21 21 219.0068; 10.478; 16.4734
90; 90; 90
1554.65Lai, Zengwei; Wang, Zhaobin; Sun, Jianwei
Organocatalytic Asymmetric Nucleophilic Addition to o-Quinone Methides by Alcohols.
Organic letters, 2015, 17, 6058-6061
1555447 CIFC21 H16 O3P b c a15.108; 7.54; 27.9119
90; 90; 90
3179.6Ravi 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 CIFC15 H12 O3P 1 21/n 17.8593; 4.0079; 36.679
90; 93.567; 90
1153.1Ravi 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 CIFC20 H30 O2C 1 2 120.0748; 6.8584; 25.9078
90; 106.399; 90
3421.9Zhou, 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 CIFC24 H36 O4P 1 21 111.623; 7.3026; 12.673
90; 95.271; 90
1071.1Zhou, 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 CIFC24 H36 O4C 1 2 131.775; 7.261; 19.184
90; 104.026; 90
4294.1Zhou, 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 CIFC24 H36 O4P 1 21 110.27; 7.257; 14.424
90; 92.479; 90
1074Zhou, 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 CIFC38 H54 O5P 21 21 2110.0955; 13.4185; 24.927
90; 90; 90
3376.8Zhou, 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 CIFC62 H84 N8 O2 S2 Si4P -18.2413; 12.7682; 15.6926
80.64; 82.824; 75.922
1574.06Cortizo-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 CIFC31 H23 Cl2 N O4 SP -19.8014; 12.1207; 13.323
99.552; 106.402; 111.742
1343.8Zhu, 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 CIFC30 H21 Cl2 N O3 SP -17.3264; 7.7051; 23.332
84.594; 88.837; 82.404
1299.7Zhu, 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 CIFC23 H18 N2 O3 SP -19.5468; 10.4076; 11.3179
103.653; 93.612; 114.414
978.53Qiao, 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 CIFC56 H40 F6 N6P 1 21/c 17.398; 11.831; 25.874
90; 94.823; 90
2256.6Tasior, 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 CIFC136 H112 OP -110.6194; 15.7603; 16.3359
73.944; 87.761; 73.938
2522.8He, 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 CIFC62.74 H45.48 Cl1.48P -19.9913; 15.4197; 15.7043
102.428; 92.308; 99.776
2321He, 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 CIFC104 H80 OP -110.2023; 12.2529; 16.1191
98.99; 102.37; 105.55
1846.7He, 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 CIFC52 H40 O0.5P -110.11; 10.19; 36.97
91.2; 94.1; 95.6
3779.3He, 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 CIFC58 H52 OC 1 2/c 130.72; 17.174; 16.373
90; 97.824; 90
8557.7He, 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 CIFC19 H17 Cl N2 O1.425P 1 21/c 113.0804; 18.104; 15.8995
90; 102.512; 90
3675.7Jiang, 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 CIFC21 H14 O4P n a 219.2786; 23.641; 7.5289
90; 90; 90
1651.5Zhao, 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 CIFC15 H12 O3P 1 21/n 113.899; 6.5834; 14.579
90; 117.751; 90
1180.6Zhao, 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 CIFC20 H14 O2P 21 21 217.3238; 9.814; 19.747
90; 90; 90
1419.3Zhao, 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 CIFC14 H10 O3P 1 21/n 110.271; 9.1771; 11.2051
90; 97.686; 90
1046.7Zhao, 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 CIFC22 H14 O3P b c a12.5409; 7.8473; 31.588
90; 90; 90
3108.6Zhao, 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 CIFC19 H14 O3P -16.866; 10.24; 11.188
69.311; 72.734; 83.093
702.6Zhao, 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 CIFC17 H13 N O3P 1 21/c 14.629; 16.421; 17.474
90; 91.158; 90
1328Zhao, 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 CIFC18 H12 O3P -17.4224; 7.787; 12.133
99.775; 91.453; 97.925
683.6Zhao, 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 CIFC21 H19 N O5P 1 21/c 19.3725; 21.712; 9.3146
90; 106.094; 90
1821.2Hong, 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 CIFC17 H22 N O3 SP 1 21 18.5345; 8.8037; 11.0062
90; 90.369; 90
826.94Moynihan, 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 CIFC13 H18 N3 O4P 1 21 16.1187; 15.5628; 7.4298
90; 90.617; 90
707.46Moynihan, 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 CIFC10 H20 O S2 SiP 1 21 16.642; 14.2879; 13.6807
90; 91.605; 90
1297.79Melillo, 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 CIFC18 H34 O S4 SiP -19.7683; 10.4783; 12.5293
102.548; 99.034; 115.038
1088.3Melillo, 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 CIFC23 H21 N OP 1 21/c 112.2975; 14.2131; 10.3046
90; 107.61; 90
1716.7Taguchi, 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 CIFC21 H18 Br NP 1 21 110.094; 14.285; 11.689
90; 90.952; 90
1685.2Zhang, Zhenhua; Du, Haifeng
Enantioselective Metal-Free Hydrogenations of Disubstituted Quinolines.
Organic letters, 2015, 17, 6266-6269
1555481 CIFC24 H24 N2 O2P 1 21/c 19.0073; 29.18; 7.8919
90; 104.587; 90
2007.39Bhojgude, 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 CIFC24 H24 N2 OP -110.369; 13.94; 14.494
83.533; 85.279; 75.051
2008.1Bhojgude, 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 CIFC25 H30 N2 O5P 1 21 18.73; 13.8357; 9.1173
90; 93.75; 90
1098.88Zhang, 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 CIFC17 H12 N2 O4P 1 21/c 113.389; 7.794; 13.881
90; 90.579; 90
1448.5Gao, 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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