Crystallography Open Database

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Searching journal of publication like 'Organic letters' volume of publication is 12

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1503084 CIFC32 H50 N2 O4P 438.2499; 8.2499; 42.596
90; 90; 90
2899.1Yang, Yu-Rong; Lai, Zeng-Wei; Shen, Liang; Huang, Jiu-Zhong; Wu, Xing-De; Yin, Jun-Lin; Wei, Kun
Total synthesis of (-)-8-deoxyserratinine via an efficient Helquist annulation and double N-alkylation reaction.
Organic letters, 2010, 12, 3430-3433
1503085 CIFC16 H13 Br O2P 1 21 19.977; 5.5033; 13.198
90; 108.25; 90
688.2Chen, Zhengwang; Li, Jinghao; Jiang, Huanfeng; Zhu, Shifa; Li, Yibiao; Qi, Chaorong
Silver-catalyzed difunctionalization of terminal alkynes: highly regio- and stereoselective synthesis of (Z)-beta-haloenol acetates.
Organic letters, 2010, 12, 3262-3265
1503086 CIFC44 H49 Ni O PP 1 21/c 112.8408; 15.1873; 18.453
90; 97.9023; 90
3564.5Ogoshi, Sensuke; Nishimura, Akira; Ohashi, Masato
Nickel-catalyzed [2 + 2 + 2] cycloaddition of two enones and an alkyne.
Organic letters, 2010, 12, 3450-3452
1503087 CIFC24 H26 O2P 1 21/a 110.2808; 15.2707; 12.1045
90; 95.07; 90
1892.91Ogoshi, Sensuke; Nishimura, Akira; Ohashi, Masato
Nickel-catalyzed [2 + 2 + 2] cycloaddition of two enones and an alkyne.
Organic letters, 2010, 12, 3450-3452
1503088 CIFC24 H26 O2P 1 21/c 16.08838; 37.5923; 9.11131
90; 114.271; 90
1901.04Ogoshi, Sensuke; Nishimura, Akira; Ohashi, Masato
Nickel-catalyzed [2 + 2 + 2] cycloaddition of two enones and an alkyne.
Organic letters, 2010, 12, 3450-3452
1503089 CIFC95 H139 Cl9 N16 O22P 21 21 221.4551; 28.4412; 8.9866
90; 90; 90
5483.7Fernandes, Carlos; Faure, Sophie; Pereira, Elisabeth; Théry, Vincent; Declerck, Valérie; Guillot, Régis; Aitken, David J.
12-Helix folding of cyclobutane beta-amino acid oligomers.
Organic letters, 2010, 12, 3606-3609
1503090 CIFC21 H12 N2 O2P 1 2/c 115.444; 7.4809; 14.862
90; 116.866; 90
1531.7Saha, Sukdeb; Ghosh, Amrita; Mahato, Prasenjit; Mishra, Sandhya; Mishra, Sanjiv K.; Suresh, E.; Das, Satyabrata; Das, Amitava
Specific recognition and sensing of CN- in sodium cyanide solution.
Organic letters, 2010, 12, 3406-3409
1503091 CIFC25 H16 Fe N2 O2P b c n27.672; 10.248; 13.417
90; 90; 90
3804.8Saha, Sukdeb; Ghosh, Amrita; Mahato, Prasenjit; Mishra, Sandhya; Mishra, Sanjiv K.; Suresh, E.; Das, Satyabrata; Das, Amitava
Specific recognition and sensing of CN- in sodium cyanide solution.
Organic letters, 2010, 12, 3406-3409
1503092 CIFC26 H22 F3 N O2 SP b c a15.2284; 17.6487; 17.8733
90; 90; 90
4803.7Minami, Yasunori; Kuniyasu, Hitoshi; Sanagawa, Atsushi; Kambe, Nobuaki
Pd-catalyzed regioselective iminothiolation of alkynes: a remarkable effect of the CF3 group of iminosulfides.
Organic letters, 2010, 12, 3744-3747
1503093 CIFC26 H24 OP 1 21 112.393; 5.8186; 14.691
90; 111.21; 90
987.6Chen, Zili; Zhang, Yu-Xin; Wang, Ya-Hui; Zhu, Li-Li; Liu, Heng; Li, Xiao-Xiao; Guo, Lin
Gold catalyzed diastereoselective cascade allylation/enyne cycloisomerization to construct densely functionalized oxygen heterocycles.
Organic letters, 2010, 12, 3468-3471
1503094 CIFC18 H20 O2P 1 21/c 123.7529; 6.5856; 17.3617
90; 90.515; 90
2715.73Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503095 CIFC18 H20 O2R -3 :H23.8832; 23.8832; 6.3231
90; 90; 120
3123.53Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503096 CIFC12 H17 Cl OP -110.9259; 11.4009; 14.825
100.201; 96.264; 115.471
1604.8Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503097 CIFC12 H17 Cl OR -3 :H22.0572; 22.0572; 11.2664
90; 90; 120
4746.97Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503098 CIFC13 H19 Cl OP 1 21/n 111.5914; 14.8542; 21.2577
90; 96.95; 90
3633.3Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503099 CIFC18 H21 Cl O2P 1 21/c 119.5539; 6.3547; 12.0615
90; 100.778; 90
1472.31Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503100 CIFC18 H21 Cl O2P b c a18.9939; 7.0672; 21.2043
90; 90; 90
2846.33Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503101 CIFC18 H22 O1.5P -16.3057; 10.0701; 11.3997
79.458; 81.737; 77.069
689.603Valiulin, Roman A.; Arisco, Teresa M.; Kutateladze, Andrei G.
Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes.
Organic letters, 2010, 12, 3398-3401
1503102 CIFC36 H55 Cl2 N O10P 21 21 2110.613; 10.756; 33.591
90; 90; 90
3834.5Igarashi, Yasuhiro; Kim, Youngju; In, Yasuko; Ishida, Toshimasa; Kan, Yukiko; Fujita, Tsuyoshi; Iwashita, Takashi; Tabata, Hirokazu; Onaka, Hiroyasu; Furumai, Tamotsu
Alchivemycin A, a bioactive polycyclic polyketide with an unprecedented skeleton from Streptomyces sp.
Organic letters, 2010, 12, 3402-3405
1503103 CIFC24 H23 F3 OP -19.5151; 9.9721; 10.8051
86.882; 89.898; 75.105
989.3Yang, Chun-Ming; Jeganmohan, Masilamani; Parthasarathy, Kanniyappan; Cheng, Chien-Hong
Highly selective nickel-catalyzed three-component coupling of alkynes with enones and alkenyl boronic acids: a novel route to substituted 1,3-dienes
Organic Letters, 2010, 12, 3610-3613
1503104 CIFC19 H20 O4P 15.3565; 7.6392; 10.099
76.068; 85.27; 86.338
399.308Yang, Chun-Ming; Jeganmohan, Masilamani; Parthasarathy, Kanniyappan; Cheng, Chien-Hong
Highly selective nickel-catalyzed three-component coupling of alkynes with enones and alkenyl boronic acids: a novel route to substituted 1,3-dienes
Organic Letters, 2010, 12, 3610-3613
1503105 CIFC11 H5 Cl F O2P 1 21/c 113.0998; 6.0571; 11.6096
90; 98.514; 90
911.03Colquhoun, Howard M.; Zhu, Zhixue; Cardin, Christine J.; White, Andrew J. P.; Drew, Michael G. B.; Gan, Yu
Bis(hydroxy-isoindolinone)s: synthesis, stereochemistry, polymer chemistry, and supramolecular assembly.
Organic letters, 2010, 12, 3756-3759
1503106 CIFC58 H34 F2 O4P -19.124; 12.5563; 15.4232
108.753; 100.834; 98.211
1603.59Colquhoun, Howard M.; Zhu, Zhixue; Cardin, Christine J.; White, Andrew J. P.; Drew, Michael G. B.; Gan, Yu
Bis(hydroxy-isoindolinone)s: synthesis, stereochemistry, polymer chemistry, and supramolecular assembly.
Organic letters, 2010, 12, 3756-3759
1503107 CIFC56 H36 F2 N2 O5C m c 2137.353; 15.704; 7.5165
90; 90; 90
4409.1Colquhoun, Howard M.; Zhu, Zhixue; Cardin, Christine J.; White, Andrew J. P.; Drew, Michael G. B.; Gan, Yu
Bis(hydroxy-isoindolinone)s: synthesis, stereochemistry, polymer chemistry, and supramolecular assembly.
Organic letters, 2010, 12, 3756-3759
1503108 CIFC78 H45 F N3 O12 S2P -112.0725; 22.6806; 32.2434
84.168; 85.204; 74.958
8466.9Colquhoun, Howard M.; Zhu, Zhixue; Cardin, Christine J.; White, Andrew J. P.; Drew, Michael G. B.; Gan, Yu
Bis(hydroxy-isoindolinone)s: synthesis, stereochemistry, polymer chemistry, and supramolecular assembly.
Organic letters, 2010, 12, 3756-3759
1503109 CIFC48 H54 F2 N6 O8P -18.572; 9.6617; 13.723
93.667; 92.869; 96.67
1124.6Colquhoun, Howard M.; Zhu, Zhixue; Cardin, Christine J.; White, Andrew J. P.; Drew, Michael G. B.; Gan, Yu
Bis(hydroxy-isoindolinone)s: synthesis, stereochemistry, polymer chemistry, and supramolecular assembly.
Organic letters, 2010, 12, 3756-3759
1503110 CIFC18 H24 O5P -17.4222; 9.2295; 13.544
85; 74.87; 84.77
890Patel, Paresma R.; Boger, Dale L.
Intramolecular Diels-Alder reactions of cyclopropenone ketals.
Organic letters, 2010, 12, 3540-3543
1503111 CIFC16 H19 N O3P 1 21/c 119.271; 9.716; 17.52
90; 117.04; 90
2921.8Patel, Paresma R.; Boger, Dale L.
Intramolecular Diels-Alder reactions of cyclopropenone ketals.
Organic letters, 2010, 12, 3540-3543
1503112 CIFC30 H21 N3 O6P -18.2637; 12.0452; 13.7503
76.768; 80.817; 69.691
1244.7Jones, Ian M.; Hamilton, Andrew D.
Designed molecular switches: controlling the conformation of benzamido-diphenylacetylenes.
Organic letters, 2010, 12, 3651-3653
1503113 CIFC22 H28 Br2 O2P -19.211; 10.794; 11.994
106.031; 96.445; 112.428
1027.1Shenvi, Ryan A.; Corey, E. J.
Synthetic access to bent polycycles by cation-pi cyclization.
Organic letters, 2010, 12, 3548-3551
1503114 CIFC58 H68 Br4 O7P 1 21 119.335; 7.4272; 20.267
90; 104.272; 90
2820.6Shenvi, Ryan A.; Corey, E. J.
Synthetic access to bent polycycles by cation-pi cyclization.
Organic letters, 2010, 12, 3548-3551
1503115 CIFC24 H30 N2 O5P 1 21/n 113.6877; 9.8076; 15.7743
90; 90.763; 90
2117.4Kulyk, Svitlana; Dougherty, Jr, William G; Kassel, W. Scott; Fleming, Steven A.; Sieburth, Scott McN
Enyne [4 + 4] photocycloaddition: bridged 1,2,5-cyclooctatrienes.
Organic letters, 2010, 12, 3296-3299
1503116 CIFC23 H25 N O4 SP 21 21 218.274; 10.2749; 23.741
90; 90; 90
2018.3Li, Hongyan; Hsung, Richard P.; DeKorver, Kyle A.; Wei, Yonggang
Copper-catalyzed Ficini [2 + 2] cycloaddition of ynamides.
Organic letters, 2010, 12, 3780-3783
1503117 CIFC33 H33 Cl3 N2 O6 SP 21 21 215.7619; 19.3032; 29.1369
90; 90; 90
3240.7Li, Meiling; Dixon, Darren J.
Stereoselective spirolactam synthesis via palladium catalyzed arylative allene carbocyclization cascades.
Organic letters, 2010, 12, 3784-3787
1503118 CIFC17 H19 N O6P -18.8667; 9.048; 11.101
105.71; 98.61; 96.29
837.1Xu, Silong; Zou, Wen; Wu, Guiping; Song, Haibin; He, Zhengjie
Stereoselective synthesis of 1,2,3,4-tetrasubstituted dienes from allenoates and aldehydes: an observation of phosphine-induced chemoselectivity.
Organic letters, 2010, 12, 3556-3559
1503119 CIFC18 H22 O4P 1 21/n 114.985; 7.503; 15.386
90; 108.888; 90
1636.7Xu, Silong; Zou, Wen; Wu, Guiping; Song, Haibin; He, Zhengjie
Stereoselective synthesis of 1,2,3,4-tetrasubstituted dienes from allenoates and aldehydes: an observation of phosphine-induced chemoselectivity.
Organic letters, 2010, 12, 3556-3559
1503120 CIFC44 H78 N6 O11P 3121.328; 21.328; 29.108
90; 90; 120
11467Nagano, Masanobu; Doi, Mitsunobu; Kurihara, Masaaki; Suemune, Hiroshi; Tanaka, Masakazu
Stabilized alpha-helix-catalyzed enantioselective epoxidation of alpha,beta-unsaturated ketones.
Organic letters, 2010, 12, 3564-3566
1503121 CIFC63 H115 N9 O17P 21 21 2112.247; 15.641; 77.051
90; 90; 90
14760Nagano, Masanobu; Doi, Mitsunobu; Kurihara, Masaaki; Suemune, Hiroshi; Tanaka, Masakazu
Stabilized alpha-helix-catalyzed enantioselective epoxidation of alpha,beta-unsaturated ketones.
Organic letters, 2010, 12, 3564-3566
1503122 CIFC84 H151 N13 O22P 111.2535; 11.6895; 19.1693
86.46; 80.779; 87.428
2482.8Nagano, Masanobu; Doi, Mitsunobu; Kurihara, Masaaki; Suemune, Hiroshi; Tanaka, Masakazu
Stabilized alpha-helix-catalyzed enantioselective epoxidation of alpha,beta-unsaturated ketones.
Organic letters, 2010, 12, 3564-3566
1503123 CIFC24 H24 N2 O6 SP 1 21/c 113.5739; 15.7377; 11.1867
90; 101.209; 90
2344.1Zhu, Zhi-Bin; Shi, Min
Ruthenium-catalyzed tandem ring-opening/ring-closing/cross-metathesis of 1,6-cyclopropene-ynes and olefins for the construction of the 3-pyrroline skeleton.
Organic letters, 2010, 12, 4462-4465
1503124 CIFC11 H14 N2 OP 1 21/c 18.925; 13.408; 17.122
90; 91.162; 90
2048.5Wei, Ying; Liu, Jing; Lin, Shaoxia; Ding, Hongqian; Liang, Fushun; Zhao, Baozhong
Acetoacetanilides as masked isocyanates: facile and efficient synthesis of unsymmetrically substituted ureas
Organic Letters, 2010, 12, 4220-4223
1503125 CIFC23 H20 Br N3 O4P -111.309; 11.587; 16.784
87.93; 80.536; 86.22
2164Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503126 CIFC22.66667 H19.66667 Cl2 N3 O4.66667P -114.308; 14.59; 19.733
101.072; 100.8; 110.784
3630.1Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503127 CIFC26 H20 Cl N3 O4P 1 21/c 111.9281; 10.2727; 22.909
90; 109.026; 90
2653.8Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503128 CIFC25 H25 Cl N2 O6P 1 21/c 110.6943; 25.494; 8.9322
90; 103.349; 90
2369.5Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503129 CIFC27 H29 Br N2 O7P -110.8467; 16.631; 17.796
112.348; 97.654; 105.826
2753.5Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503130 CIFC28 H25 Cl N2 O6P -110.3872; 11.3862; 11.9876
69.288; 72.049; 85.319
1261Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503131 CIFC29 H33 Cl N2 O5P -17.9609; 11.5503; 15.081
78.065; 83.794; 89.496
1348.7Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503132 CIFC28 H30 Cl2 N2 O5P -110.8157; 12.2522; 12.6256
101.082; 110.327; 109.908
1380.6Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681
1503133 CIFC23 H22 Cl N3 O5P 1 21/c 111.156; 26.984; 11.394
90; 110.121; 90
3221Sun, Jing; Xia, Er-Yan; Wu, Qun; Yan, Chao-Guo
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate.
Organic letters, 2010, 12, 3678-3681

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