Crystallography Open Database

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Searching journal of publication like 'Organic letters' volume of publication is 14

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1508672 CIFC30 H27 Cl N2 O3P 1 21/c 19.2972; 28.872; 10.5273
90; 108.994; 90		2672Jiang, Bo; Li, Qiu-Yun; Tu, Shu-Jiang; Li, Guigen
Three-component domino reactions for selective formation of indeno[1,2-b]indole derivatives.
Organic letters, 2012, 14, 5210-5213
1508673 CIFC24 H17 N O3P 1 21/c 111.2385; 13.7508; 11.8921
90; 95.111; 90		1830.5Jiang, Bo; Li, Qiu-Yun; Tu, Shu-Jiang; Li, Guigen
Three-component domino reactions for selective formation of indeno[1,2-b]indole derivatives.
Organic letters, 2012, 14, 5210-5213
1508674 CIFC28 H25.5 F N2 O4.5C 1 2/c 114.6566; 15.3994; 21.545
90; 94.645; 90		4846.8Jiang, Bo; Li, Qiu-Yun; Tu, Shu-Jiang; Li, Guigen
Three-component domino reactions for selective formation of indeno[1,2-b]indole derivatives.
Organic letters, 2012, 14, 5210-5213
1508675 CIFC30 H27 N O5 SP -19.6216; 11.7391; 12.5857
70.506; 75.876; 75.746		1278.3Hu, Jian; Tian, Bing; Wu, Xinyan; Tong, Xiaofeng
Tertiary amine-triggered cascade S(N)2/cycloaddition: an efficient construction of complex azaheterocycles under mild conditions.
Organic letters, 2012, 14, 5074-5077
1508676 CIFC19 H19 B F2 N4 OP n a 2113.339; 18.975; 6.8571
90; 90; 90		1735.6Wu, Yun-Ying; Chen, Yong; Gou, Gao-Zhang; Mu, Wei-Hua; Lv, Xiao-Jun; Du, Mei-Ling; Fu, Wen-Fu
Large Stokes shift induced by intramolcular charge transfer in N,O-chelated naphthyridine-BF2 complexes.
Organic letters, 2012, 14, 5226-5229
1508677 CIFC19 H13 B F8 N4 OP 1 21/n 110.873; 14.773; 11.623
90; 92.752; 90		1864.8Wu, Yun-Ying; Chen, Yong; Gou, Gao-Zhang; Mu, Wei-Hua; Lv, Xiao-Jun; Du, Mei-Ling; Fu, Wen-Fu
Large Stokes shift induced by intramolcular charge transfer in N,O-chelated naphthyridine-BF2 complexes.
Organic letters, 2012, 14, 5226-5229
1508678 CIFC17 H14 B F2 N3 OC 1 2/c 118.636; 10.788; 15.333
90; 94.98; 90		3071Wu, Yun-Ying; Chen, Yong; Gou, Gao-Zhang; Mu, Wei-Hua; Lv, Xiao-Jun; Du, Mei-Ling; Fu, Wen-Fu
Large Stokes shift induced by intramolcular charge transfer in N,O-chelated naphthyridine-BF2 complexes.
Organic letters, 2012, 14, 5226-5229
1508679 CIFC17 H16 N3 O1.5C 1 2/c 125.865; 7.4047; 15.416
90; 97.89; 90		2924.6Wu, Yun-Ying; Chen, Yong; Gou, Gao-Zhang; Mu, Wei-Hua; Lv, Xiao-Jun; Du, Mei-Ling; Fu, Wen-Fu
Large Stokes shift induced by intramolcular charge transfer in N,O-chelated naphthyridine-BF2 complexes.
Organic letters, 2012, 14, 5226-5229
1508680 CIFC18 H15 N2 O0.5C 1 2/c 123.4787; 6.9212; 16.9815
90; 107.401; 90		2633.2Ammermann, Sven; Hrib, Christian; Jones, Peter G.; du Mont, Wolf-Walther; Kowalsky, Wolfgang; Johannes, Hans-Hermann
Pyrrolo[1,2-a]quinoxalines: novel synthesis via annulation of 2-alkylquinoxalines.
Organic letters, 2012, 14, 5090-5093
1508681 CIFC19 H16 N2P 1 21/n 18.3778; 11.2485; 15.3805
90; 103.626; 90		1408.63Ammermann, Sven; Hrib, Christian; Jones, Peter G.; du Mont, Wolf-Walther; Kowalsky, Wolfgang; Johannes, Hans-Hermann
Pyrrolo[1,2-a]quinoxalines: novel synthesis via annulation of 2-alkylquinoxalines.
Organic letters, 2012, 14, 5090-5093
1508682 CIFC15 H8 Br N OP 1 21/n 111.0306; 3.906; 26.505
90; 91.877; 90		1141.37Choi, Young Lok; Lim, Hye Sun; Lim, Hwan Jung; Heo, Jung-Nyoung
One-pot transition-metal-free synthesis of dibenzo[b,f]oxepins from 2-halobenzaldehydes.
Organic letters, 2012, 14, 5102-5105
1508683 CIFC20 H22 O3P b c a9.3; 18.67; 19.8
90; 90; 90		3438Yang, Ming; Wang, Lin; He, Zheng-He; Wang, Shao-Hua; Zhang, Shu-Yu; Tu, Yong-Qiang; Zhang, Fu-Min
Tandem semipinacol-type 1,2-carbon migration/aldol reaction toward the construction of [5-6-7] all-carbon tricyclic core of Calyciphylline A-type alkaloids.
Organic letters, 2012, 14, 5114-5117
1508684 CIFC15 H22 O2P -18.404; 12.59; 12.974
97.43; 103.628; 96.743		1307.2Yang, Ming; Wang, Lin; He, Zheng-He; Wang, Shao-Hua; Zhang, Shu-Yu; Tu, Yong-Qiang; Zhang, Fu-Min
Tandem semipinacol-type 1,2-carbon migration/aldol reaction toward the construction of [5-6-7] all-carbon tricyclic core of Calyciphylline A-type alkaloids.
Organic letters, 2012, 14, 5114-5117
1508685 CIFC17 H24 Br Cl N2 O5 SP 1 21/c 17.2934; 10.8198; 26.137
90; 91.847; 90		2061.5Zhou, Jing; Zhou, Ling; Yeung, Ying-Yeung
Multicomponent approach in the synthesis of 2,2,6-trisubstituted morpholine derivatives.
Organic letters, 2012, 14, 5250-5253
1508686 CIFC17 H23 Cl N2 O5 SP b c a11.4136; 11.557; 28.331
90; 90; 90		3737.1Zhou, Jing; Zhou, Ling; Yeung, Ying-Yeung
Multicomponent approach in the synthesis of 2,2,6-trisubstituted morpholine derivatives.
Organic letters, 2012, 14, 5250-5253
1508687 CIFC18 H23 Cl N2 O7 SC 1 2/c 133.128; 11.5838; 10.9008
90; 106.391; 90		4013.2Zhou, Jing; Zhou, Ling; Yeung, Ying-Yeung
Multicomponent approach in the synthesis of 2,2,6-trisubstituted morpholine derivatives.
Organic letters, 2012, 14, 5250-5253
1508688 CIFC60 H68 O12P 21 21 2110.8909; 13.7047; 34.1253
90; 90; 90		5093.4Shao, Meng; Wang, Ying; Jian, Yu-Qing; Huang, Xiao-Jun; Zhang, Dong-Mei; Tang, Qing-Fa; Jiang, Ren-Wang; Sun, Xue-Gang; Lv, Zhi-Ping; Zhang, Xiao-Qi; Ye, Wen-Cai
Guadial A and psiguadials C and D, three unusual meroterpenoids from Psidium guajava.
Organic letters, 2012, 14, 5262-5265
1508689 CIFC30 H19 N3 OP 1 21/n 19.2006; 19.587; 11.9092
90; 104.475; 90		2078.1Hao, Wen-Juan; Xu, Xiao-Ping; Bai, Hui-Wen; Wang, Shun-Yi; Ji, Shun-Jun
Efficient multicomponent strategy to pentacyclic pyrazole-fused naphtho[1,8-fg]isoquinolines through cleavage of two carbon-carbon bonds.
Organic letters, 2012, 14, 4894-4897
1508690 CIFC17 H21 Cl N2 O4P 1 21 114.9959; 7.1013; 18.0983
90; 113.682; 90		1765Barber, David M.; Sanganee, Hitesh J.; Dixon, Darren J.
One-pot catalytic enantioselective synthesis of tetrahydropyridines via a nitro-Mannich/hydroamination cascade.
Organic letters, 2012, 14, 5290-5293
1508691 CIFC20 H27 N O4P 1 21 112.5953; 6.309; 12.71
90; 110.532; 90		945.83Mukaeda, Yuki; Kato, Takuya; Hosokawa, Seijiro
Syn-selective Kobayashi aldol reaction using the E,E-vinylketene silyl N,O-acetal.
Organic letters, 2012, 14, 5298-5301
1508692 CIFC19 H24 Br N O4C 1 2 125.422; 6.1383; 12.182
90; 98.781; 90		1878.7Mukaeda, Yuki; Kato, Takuya; Hosokawa, Seijiro
Syn-selective Kobayashi aldol reaction using the E,E-vinylketene silyl N,O-acetal.
Organic letters, 2012, 14, 5298-5301
1508693 CIFC19 H24 N2 O6C 1 2 124.942; 6.13836; 12.4356
90; 97.4055; 90		1888.05Mukaeda, Yuki; Kato, Takuya; Hosokawa, Seijiro
Syn-selective Kobayashi aldol reaction using the E,E-vinylketene silyl N,O-acetal.
Organic letters, 2012, 14, 5298-5301
1508694 CIFC23 H29 N3 O9P 1 21 110.2747; 12.2094; 10.319
90; 111.243; 90		1206.54Mukaeda, Yuki; Kato, Takuya; Hosokawa, Seijiro
Syn-selective Kobayashi aldol reaction using the E,E-vinylketene silyl N,O-acetal.
Organic letters, 2012, 14, 5298-5301
1508695 CIFC15 H16 O5P 21 21 215.7572; 11.6775; 19.3379
90; 90; 90		1300.08Yang, Xiao-Yan; Feng, Tao; Li, Zheng-Hui; Sheng, Yu; Yin, Xia; Leng, Ying; Liu, Ji-Kai
Conosilane A, an unprecedented sesquiterpene from the cultures of basidiomycete Conocybe siliginea.
Organic letters, 2012, 14, 5382-5384
1508696 CIFC20 H31 Br N2 O5P 18.0748; 15.1323; 29.19
98.815; 92.189; 105.25		3388.9Goldberg, Alexander F. G.; O'Connor, Nicholas R; Craig, 2nd, Robert A; Stoltz, Brian M.
Lewis acid mediated (3 + 2) cycloadditions of donor-acceptor cyclopropanes with heterocumulenes.
Organic letters, 2012, 14, 5314-5317
1508697 CIFC20 H25 N O4 SP 1 21/c 114.5982; 16.162; 8.2014
90; 92.145; 90		1933.7Goldberg, Alexander F. G.; O'Connor, Nicholas R; Craig, 2nd, Robert A; Stoltz, Brian M.
Lewis acid mediated (3 + 2) cycloadditions of donor-acceptor cyclopropanes with heterocumulenes.
Organic letters, 2012, 14, 5314-5317
1508698 CIFC13 H24 N O3P 1 21/c 18.5917; 14.176; 11.4969
90; 97.865; 90		1387.1Paletta, Joseph T.; Pink, Maren; Foley, Bridget; Rajca, Suchada; Rajca, Andrzej
Synthesis and reduction kinetics of sterically shielded pyrrolidine nitroxides.
Organic letters, 2012, 14, 5322-5325
1508699 CIFC15 H23 N O3P 1 21/m 18.025; 9.9052; 8.9614
90; 92.41; 90		711.7Paletta, Joseph T.; Pink, Maren; Foley, Bridget; Rajca, Suchada; Rajca, Andrzej
Synthesis and reduction kinetics of sterically shielded pyrrolidine nitroxides.
Organic letters, 2012, 14, 5322-5325
1508700 CIFC15 H24 N O2P 1 21/c 111.5624; 11.0144; 10.9255
90; 104.417; 90		1347.6Paletta, Joseph T.; Pink, Maren; Foley, Bridget; Rajca, Suchada; Rajca, Andrzej
Synthesis and reduction kinetics of sterically shielded pyrrolidine nitroxides.
Organic letters, 2012, 14, 5322-5325
1508701 CIFC13 H18 N2 O3 SP 1 21/c 110.1217; 5.2676; 25.2607
90; 98.691; 90		1331.36Lu, Hongjian; Hu, Yang; Jiang, Huiling; Wojtas, Lukasz; Zhang, X. Peter
Stereoselective radical amination of electron-deficient C(sp3)-H bonds by Co(II)-based metalloradical catalysis: direct synthesis of α-amino acid derivatives via α-C-H amination.
Organic letters, 2012, 14, 5158-5161
1508702 CIFC16 H22 N2 O3 SP 1 21/n 15.099; 15.0874; 20.8353
90; 96.234; 90		1593.39Lu, Hongjian; Hu, Yang; Jiang, Huiling; Wojtas, Lukasz; Zhang, X. Peter
Stereoselective radical amination of electron-deficient C(sp3)-H bonds by Co(II)-based metalloradical catalysis: direct synthesis of α-amino acid derivatives via α-C-H amination.
Organic letters, 2012, 14, 5158-5161
1508703 CIFC16 H22 N2 O3 SP 1 21/c 110.5533; 14.5967; 10.1764
90; 96.78; 90		1556.64Lu, Hongjian; Hu, Yang; Jiang, Huiling; Wojtas, Lukasz; Zhang, X. Peter
Stereoselective radical amination of electron-deficient C(sp3)-H bonds by Co(II)-based metalloradical catalysis: direct synthesis of α-amino acid derivatives via α-C-H amination.
Organic letters, 2012, 14, 5158-5161
1508704 CIFC40 H68 B2 O6 Si2P -17.7423; 11.828; 12.677
73.699; 86.956; 83.755		1107.3Nakano, Masahiro; Shinamura, Shoji; Sugimoto, Ryusuke; Osaka, Itaru; Miyazaki, Eigo; Takimiya, Kazuo
Borylation on benzo[1,2-b:4,5-b']- and naphtho[1,2-b:5,6-b']dichalcogenophenes: different chalcogene atom effects on borylation reaction depending on fused ring structure.
Organic letters, 2012, 14, 5448-5451
1508705 CIFC40 H68 B2 O4 S2 Si2P 1 21 112.3238; 13.3375; 14.9419
90; 113.697; 90		2248.9Nakano, Masahiro; Shinamura, Shoji; Sugimoto, Ryusuke; Osaka, Itaru; Miyazaki, Eigo; Takimiya, Kazuo
Borylation on benzo[1,2-b:4,5-b']- and naphtho[1,2-b:5,6-b']dichalcogenophenes: different chalcogene atom effects on borylation reaction depending on fused ring structure.
Organic letters, 2012, 14, 5448-5451
1508706 CIFC40 H68 B2 O4 Se2 Si2P 1 21/n 112.433; 13.331; 14.725
90; 113.371; 90		2240Nakano, Masahiro; Shinamura, Shoji; Sugimoto, Ryusuke; Osaka, Itaru; Miyazaki, Eigo; Takimiya, Kazuo
Borylation on benzo[1,2-b:4,5-b']- and naphtho[1,2-b:5,6-b']dichalcogenophenes: different chalcogene atom effects on borylation reaction depending on fused ring structure.
Organic letters, 2012, 14, 5448-5451
1508707 CIFC28 H30 N2 O4 SP 1 21/n 111.5309; 8.303; 27.839
90; 98.03; 90		2639.2Li, Guifei; Ding, Zhengwei; Xu, Bin
Rhodium-catalyzed oxidative annulation of sulfonylhydrazones with alkenes.
Organic letters, 2012, 14, 5338-5341
1508708 CIFC18 H18 O5 SP 21 21 218.6017; 8.8242; 21.789
90; 90; 90		1653.9Hong, Bor-Cherng; Dange, Nitin S.; Yen, Po-Jen; Lee, Gene-Hsiang; Liao, Ju-Hsiou
Organocatalytic asymmetric anti-selective Michael reactions of aldehydes and the sequential reduction/lactonization/Pauson-Khand reaction for the enantioselective synthesis of highly functionalized hydropentalenes.
Organic letters, 2012, 14, 5346-5349
1508709 CIFC18 H18 O5 SP 21 21 218.548; 8.7031; 21.6417
90; 90; 90		1610.01Hong, Bor-Cherng; Dange, Nitin S.; Yen, Po-Jen; Lee, Gene-Hsiang; Liao, Ju-Hsiou
Organocatalytic asymmetric anti-selective Michael reactions of aldehydes and the sequential reduction/lactonization/Pauson-Khand reaction for the enantioselective synthesis of highly functionalized hydropentalenes.
Organic letters, 2012, 14, 5346-5349
1508710 CIFC18 H18 O5 SP 21 21 218.5503; 8.7108; 21.6531
90; 90; 90		1612.72Hong, Bor-Cherng; Dange, Nitin S.; Yen, Po-Jen; Lee, Gene-Hsiang; Liao, Ju-Hsiou
Organocatalytic asymmetric anti-selective Michael reactions of aldehydes and the sequential reduction/lactonization/Pauson-Khand reaction for the enantioselective synthesis of highly functionalized hydropentalenes.
Organic letters, 2012, 14, 5346-5349
1508711 CIFC18 H18 O5 SP 21 21 218.6054; 8.8177; 21.769
90; 90; 90		1651.8Hong, Bor-Cherng; Dange, Nitin S.; Yen, Po-Jen; Lee, Gene-Hsiang; Liao, Ju-Hsiou
Organocatalytic asymmetric anti-selective Michael reactions of aldehydes and the sequential reduction/lactonization/Pauson-Khand reaction for the enantioselective synthesis of highly functionalized hydropentalenes.
Organic letters, 2012, 14, 5346-5349
1508712 CIFC20 H20 O5P 1 21/c 110.7107; 8.0875; 19.702
90; 101.638; 90		1671.6Hong, Bor-Cherng; Dange, Nitin S.; Yen, Po-Jen; Lee, Gene-Hsiang; Liao, Ju-Hsiou
Organocatalytic asymmetric anti-selective Michael reactions of aldehydes and the sequential reduction/lactonization/Pauson-Khand reaction for the enantioselective synthesis of highly functionalized hydropentalenes.
Organic letters, 2012, 14, 5346-5349
1508713 CIFC61 H52 Cl2 N4 O8P -110.4767; 14.011; 20.104
103.149; 94.146; 109.798		2667.7Sun, Jing; Sun, Yan; Gong, Hui; Xie, Ya-Jing; Yan, Chao-Guo
Facile synthesis of dispirooxindole-fused heterocycles via domino 1,4-dipolar addition and Diels-Alder reaction of in situ generated Huisgen 1,4-dipoles.
Organic letters, 2012, 14, 5172-5175
1508714 CIFC61 H50 Cl4 N4 O8P -110.4418; 14.56; 20.248
103.886; 92.639; 110.608		2768.2Sun, Jing; Sun, Yan; Gong, Hui; Xie, Ya-Jing; Yan, Chao-Guo
Facile synthesis of dispirooxindole-fused heterocycles via domino 1,4-dipolar addition and Diels-Alder reaction of in situ generated Huisgen 1,4-dipoles.
Organic letters, 2012, 14, 5172-5175
1508715 CIFC24 H22 Cl N3 O3P 1 21/c 17.611; 9.414; 30.428
90; 94.599; 90		2173.1Sun, Jing; Sun, Yan; Gong, Hui; Xie, Ya-Jing; Yan, Chao-Guo
Facile synthesis of dispirooxindole-fused heterocycles via domino 1,4-dipolar addition and Diels-Alder reaction of in situ generated Huisgen 1,4-dipoles.
Organic letters, 2012, 14, 5172-5175
1508716 CIFC35 H29 Cl N2 O6P -110.5885; 12.3008; 13.451
112.414; 100.134; 98.715		1547.6Sun, Jing; Sun, Yan; Gong, Hui; Xie, Ya-Jing; Yan, Chao-Guo
Facile synthesis of dispirooxindole-fused heterocycles via domino 1,4-dipolar addition and Diels-Alder reaction of in situ generated Huisgen 1,4-dipoles.
Organic letters, 2012, 14, 5172-5175
1508717 CIFC36 H31 Cl N2 O6P 1 21/c 112.882; 13.095; 18.933
90; 99.562; 90		3149Sun, Jing; Sun, Yan; Gong, Hui; Xie, Ya-Jing; Yan, Chao-Guo
Facile synthesis of dispirooxindole-fused heterocycles via domino 1,4-dipolar addition and Diels-Alder reaction of in situ generated Huisgen 1,4-dipoles.
Organic letters, 2012, 14, 5172-5175
1508718 CIFC23 H30 N4 O9P 21 21 216.9403; 14.831; 24.1141
90; 90; 90		2482.1Asai, Teigo; Morita, Shuntaro; Shirata, Naoki; Taniguchi, Tohru; Monde, Kenji; Sakurai, Hiroaki; Ozeki, Tomoji; Oshima, Yoshiteru
Structural diversity of new C13-polyketides produced by Chaetomium mollipilium cultivated in the presence of a NAD(+)-dependent histone deacetylase inhibitor.
Organic letters, 2012, 14, 5456-5459
1508719 CIFC33 H49 N O6 SiP 1 21/c 110.3589; 30.3196; 11.4539
90; 115.063; 90		3258.69Donohoe, Timothy J.; O'Riordan, Timothy J C; Peifer, Manuel; Jones, Christopher R.; Miles, Timothy J.
Asymmetric synthesis of the fully elaborated pyrrolidinone core of oxazolomycin A.
Organic letters, 2012, 14, 5460-5463
1508720 CIFC31 H43 N O8 SiP 21 21 219.5047; 13.4605; 24.465
90; 90; 90		3130Donohoe, Timothy J.; O'Riordan, Timothy J C; Peifer, Manuel; Jones, Christopher R.; Miles, Timothy J.
Asymmetric synthesis of the fully elaborated pyrrolidinone core of oxazolomycin A.
Organic letters, 2012, 14, 5460-5463
1508721 CIFC30 H38 N2 O6 S2P 1 21/c 110.2052; 18.7686; 16.2613
90; 101.595; 90		3051.1Gharpure, Santosh J.; Niranjana, P.; Porwal, Suheel K.
Stereoselective synthesis of oxa- and aza-angular triquinanes using tandem radical cyclization to vinylogous carbonates and carbamates.
Organic letters, 2012, 14, 5476-5479

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