Crystallography Open Database
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Searching journal of publication like 'Organic letters' volume of publication is 18
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1555755 | CIF | C28 H27 N O2 | P -1 | 11.3527; 11.6672; 16.7434 96.567; 95.824; 102.162 | 2135.7 | Huang, Yu-Wen; Frontier, Alison J. Nazarov Cyclization/Internal Redox Cyclization Sequence for the Synthesis of N-Heterocyclic Bridged Ring Systems. Organic letters, 2016, 18, 4896-4899 |
| 1555756 | CIF | C24 H23 N O3 | P 21 21 21 | 6.9578; 11.041; 24.685 90; 90; 90 | 1896.3 | Huang, Yu-Wen; Frontier, Alison J. Nazarov Cyclization/Internal Redox Cyclization Sequence for the Synthesis of N-Heterocyclic Bridged Ring Systems. Organic letters, 2016, 18, 4896-4899 |
| 1555757 | CIF | C21 H22 N2 O3 | P -1 | 8.5529; 9.1794; 12.3004 75.507; 77.927; 82.204 | 910.75 | Foley, Christopher; Shaw, Arthur; Hulme, Christopher Two-Step Route to Diverse N-Functionalized Peptidomimetic-like Isatins through an Oxidation/Intramolecular Oxidative-Amidation Cascade of Ugi Azide and Ugi Three-Component Reaction Products. Organic letters, 2016, 18, 4904-4907 |
| 1555758 | CIF | C25 H23 N O4 | P 1 21/c 1 | 8.1296; 15.4679; 33.0511 90; 94.9069; 90 | 4140.9 | Chen, Cuili; Zou, Yongzhen; Chen, Xianxiao; Zhang, Xiaoxiang; Rao, Weidong; Chan, Philip Wai Hong Gold-Catalyzed Tandem 1,3-Migration/Double Cyclopropanation of 1-Ene-4,n-diyne Esters to Tetracyclodecene and Tetracycloundecene Derivatives. Organic letters, 2016, 18, 4730-4733 |
| 1555759 | CIF | C17 H18 O | P 1 21/c 1 | 8.1119; 15.0586; 10.8705 90; 101.345; 90 | 1301.93 | Chen, Cuili; Zou, Yongzhen; Chen, Xianxiao; Zhang, Xiaoxiang; Rao, Weidong; Chan, Philip Wai Hong Gold-Catalyzed Tandem 1,3-Migration/Double Cyclopropanation of 1-Ene-4,n-diyne Esters to Tetracyclodecene and Tetracycloundecene Derivatives. Organic letters, 2016, 18, 4730-4733 |
| 1555760 | CIF | C25 H27 O6 | P 1 21/c 1 | 11.481; 13.8874; 14.2299 90; 111.405; 90 | 2112.3 | Qiao, Chuang; Zhang, Wen; Han, Jing-Chun; Li, Chuang-Chuang Catalytic Enantioselective Total Synthesis of Hypocrolide A. Organic letters, 2016, 18, 4932-4935 |
| 1555761 | CIF | C29 H30 N2 O8 | P 1 21/c 1 | 28.362; 5.9866; 16.1832 90; 100.97; 90 | 2697.6 | Qiao, Chuang; Zhang, Wen; Han, Jing-Chun; Li, Chuang-Chuang Catalytic Enantioselective Total Synthesis of Hypocrolide A. Organic letters, 2016, 18, 4932-4935 |
| 1555762 | CIF | C15 H24 O4 | P 1 21/c 1 | 9.22; 9.221; 17.022 90; 95.108; 90 | 1441.4 | Qiao, Chuang; Zhang, Wen; Han, Jing-Chun; Li, Chuang-Chuang Catalytic Enantioselective Total Synthesis of Hypocrolide A. Organic letters, 2016, 18, 4932-4935 |
| 1555763 | CIF | C25 H26 O6 | P n a 21 | 15.6433; 8.7737; 31.105 90; 90; 90 | 4269.1 | Qiao, Chuang; Zhang, Wen; Han, Jing-Chun; Li, Chuang-Chuang Catalytic Enantioselective Total Synthesis of Hypocrolide A. Organic letters, 2016, 18, 4932-4935 |
| 1555764 | CIF | C17 H18 N O6 | C 1 2 1 | 20.9111; 10.4665; 15.9414 90; 105.059; 90 | 3369.21 | Qiao, Chuang; Zhang, Wen; Han, Jing-Chun; Li, Chuang-Chuang Catalytic Enantioselective Total Synthesis of Hypocrolide A. Organic letters, 2016, 18, 4932-4935 |
| 1555765 | CIF | C23 H30 N2 O7 | P 1 21/n 1 | 9.0774; 15.15; 16.882 90; 93.62; 90 | 2317 | Yang, Changjiang; Liu, Wei; He, Zijian; He, Zhengjie Divergent Reactivity of Nitrocyclopropanes with Huisgen Zwitterions and Facile Syntheses of 3-Alkoxy Pyrazolines and Pyrazoles. Organic letters, 2016, 18, 4936-4939 |
| 1555766 | CIF | C13 H13 Br N2 O3 | P -1 | 8.296; 8.793; 10.13 100.061; 106.015; 108.472 | 645.2 | Yang, Changjiang; Liu, Wei; He, Zijian; He, Zhengjie Divergent Reactivity of Nitrocyclopropanes with Huisgen Zwitterions and Facile Syntheses of 3-Alkoxy Pyrazolines and Pyrazoles. Organic letters, 2016, 18, 4936-4939 |
| 1555767 | CIF | C19 H21 N O2 | P 21 21 21 | 5.3836; 31.775; 9.5511 90; 90; 90 | 1633.85 | Lynch, Denis; Deasy, Rebecca E.; Clarke, Leslie-Ann; Slattery, Catherine N.; Khandavilli, U. B. Rao; Lawrence, Simon E.; Maguire, Anita R.; Magnus, Nicholas A.; Moynihan, Humphrey A. Exploring the Scope of Asymmetric Synthesis of β-Hydroxy-γ-lactams via Noyori-type Reductions. Organic letters, 2016, 18, 4978-4981 |
| 1555768 | CIF | C19 H27 N O2 | P 1 21 1 | 11.0767; 6.1023; 13.1637 90; 104.848; 90 | 860.07 | Lynch, Denis; Deasy, Rebecca E.; Clarke, Leslie-Ann; Slattery, Catherine N.; Khandavilli, U. B. Rao; Lawrence, Simon E.; Maguire, Anita R.; Magnus, Nicholas A.; Moynihan, Humphrey A. Exploring the Scope of Asymmetric Synthesis of β-Hydroxy-γ-lactams via Noyori-type Reductions. Organic letters, 2016, 18, 4978-4981 |
| 1555769 | CIF | C25 H29 N O9 S | P 1 21/c 1 | 21.365; 9.334; 26.587 90; 92.256; 90 | 5298 | Ghosh, Asit; Mandal, Subhajit; Chattaraj, Pratim Kumar; Banerjee, Prabal Ring Expansion of Donor-Acceptor Cyclopropane via Substituent Controlled Selective N-Transfer of Oxaziridine: Synthetic and Mechanistic Insights. Organic letters, 2016, 18, 4940-4943 |
| 1555770 | CIF | C26 H31 N O6 | C 1 2/c 1 | 21.286; 12.49; 20.712 90; 118.061; 90 | 4859 | Ghosh, Asit; Mandal, Subhajit; Chattaraj, Pratim Kumar; Banerjee, Prabal Ring Expansion of Donor-Acceptor Cyclopropane via Substituent Controlled Selective N-Transfer of Oxaziridine: Synthetic and Mechanistic Insights. Organic letters, 2016, 18, 4940-4943 |
| 1555771 | CIF | C49 H53 B3 F6 N6 | P b n m | 8.651; 18.3861; 29.434 90; 90; 90 | 4681.7 | Ozdemir, Tugba; Bila, Jose Luis; Sozmen, Fazli; Yildirim, Leyla T.; Akkaya, Engin U. Orthogonal Bodipy Trimers as Photosensitizers for Photodynamic Action. Organic letters, 2016, 18, 4821-4823 |
| 1555772 | CIF | C35 H33 N O6 | P -1 | 8.6021; 11.6111; 16.938 70.766; 89.038; 68.763 | 1478.7 | Luo, Hejiang; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa A Route to Polysubstituted Aziridines from Carbenes and Imines through a Nondiazo Approach. Organic letters, 2016, 18, 5208-5211 |
| 1555773 | CIF | C28 H25 N O2 | P -1 | 9.92; 11.199; 12.122 64.365; 68.38; 81.92 | 1128.4 | Luo, Hejiang; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa A Route to Polysubstituted Aziridines from Carbenes and Imines through a Nondiazo Approach. Organic letters, 2016, 18, 5208-5211 |
| 1555774 | CIF | C37 H41 N3 O6 | P -1 | 11.0788; 11.3956; 13.782 74.825; 88.857; 85.704 | 1674.6 | Luo, Hejiang; Chen, Kai; Jiang, Huanfeng; Zhu, Shifa A Route to Polysubstituted Aziridines from Carbenes and Imines through a Nondiazo Approach. Organic letters, 2016, 18, 5208-5211 |
| 1555775 | CIF | C9 H8 Cl N O2 | P 21 21 21 | 5.961; 7.819; 20.316 90; 90; 90 | 946.9 | Gao, Mingchun; Xu, Bin Copper Nitrate Mediated Regio- and Stereoselective Difunctionalization of Alkynes: A Direct Approach to α-Chloro-β-nitroolefins. Organic letters, 2016, 18, 4746-4749 |
| 1555776 | CIF | C10 H8 N2 O2 S | P 21 21 21 | 6.758; 8.245; 18.741 90; 90; 90 | 1044.2 | Gao, Mingchun; Xu, Bin Copper Nitrate Mediated Regio- and Stereoselective Difunctionalization of Alkynes: A Direct Approach to α-Chloro-β-nitroolefins. Organic letters, 2016, 18, 4746-4749 |
| 1555777 | CIF | C14 H18 N2 O2 | P 1 21/c 1 | 8.018; 16.118; 10.272 90; 94.878; 90 | 1322.7 | Gao, Mingchun; Xu, Bin Copper Nitrate Mediated Regio- and Stereoselective Difunctionalization of Alkynes: A Direct Approach to α-Chloro-β-nitroolefins. Organic letters, 2016, 18, 4746-4749 |
| 1555778 | CIF | C21 H18 O2 | P 21 21 21 | 12.151; 23.564; 5.864 90; 90; 90 | 1679 | Li, Jingfu; Chang, Wenju; Ren, Wenlong; Dai, Jie; Shi, Yian Palladium-Catalyzed Highly Regio- and Enantioselective Hydroesterification of Aryl Olefins with Phenyl Formate. Organic letters, 2016, 18, 5456-5459 |
| 1555779 | CIF | C21 H24 Br2 O3 | P -1 | 10.2906; 13.6532; 15.2519 81.694; 78.662; 68.752 | 1951.9 | Shen, Minxing; Kretschmer, Manuel; Brill, Zachary G.; Snyder, Scott A. Strategies for the Total Synthesis of Diverse Bromo-Chamigrenes. Organic letters, 2016, 18, 5018-5021 |
| 1555780 | CIF | C14 H21 Br O | P 1 21/c 1 | 15.8482; 6.3578; 12.9413 90; 90.951; 90 | 1303.78 | Shen, Minxing; Kretschmer, Manuel; Brill, Zachary G.; Snyder, Scott A. Strategies for the Total Synthesis of Diverse Bromo-Chamigrenes. Organic letters, 2016, 18, 5018-5021 |
| 1555781 | CIF | C15 H25 Br O2 | P n a 21 | 10.9219; 22.3462; 13.7789 90; 90; 90 | 3362.9 | Shen, Minxing; Kretschmer, Manuel; Brill, Zachary G.; Snyder, Scott A. Strategies for the Total Synthesis of Diverse Bromo-Chamigrenes. Organic letters, 2016, 18, 5018-5021 |
| 1555782 | CIF | C14 H21 Br O | P 1 21/c 1 | 6.2175; 13.6079; 15.1894 90; 93.374; 90 | 1282.9 | Shen, Minxing; Kretschmer, Manuel; Brill, Zachary G.; Snyder, Scott A. Strategies for the Total Synthesis of Diverse Bromo-Chamigrenes. Organic letters, 2016, 18, 5018-5021 |
| 1555783 | CIF | C15 H25 Br O2 | C 1 2/c 1 | 31.909; 22.347; 13.1317 90; 97.044; 90 | 9293.2 | Shen, Minxing; Kretschmer, Manuel; Brill, Zachary G.; Snyder, Scott A. Strategies for the Total Synthesis of Diverse Bromo-Chamigrenes. Organic letters, 2016, 18, 5018-5021 |
| 1555784 | CIF | C31 H27 N O6 S | P -1 | 10.8777; 11.0084; 13.1029 112.434; 105.665; 98.631 | 1338.75 | Yang, Yanyan; Liu, Hongxu; Peng, Cheng; Wu, Jie; Zhang, Jingyi; Qiao, Yan; Wang, Xiao-Na; Chang, Junbiao AlCl<sub>3</sub>-Catalyzed Annulations of Ynamides Involving a Torquoselective Process for the Simultaneous Control of Central and Axial Chirality. Organic letters, 2016, 18, 5022-5025 |
| 1555785 | CIF | C31 H25 N O7 S | P -1 | 10.0018; 11.5034; 12.0989 88.001; 75.075; 78.255 | 1316.69 | Yang, Yanyan; Liu, Hongxu; Peng, Cheng; Wu, Jie; Zhang, Jingyi; Qiao, Yan; Wang, Xiao-Na; Chang, Junbiao AlCl<sub>3</sub>-Catalyzed Annulations of Ynamides Involving a Torquoselective Process for the Simultaneous Control of Central and Axial Chirality. Organic letters, 2016, 18, 5022-5025 |
| 1555786 | CIF | C32 H29 N O6 S | P 1 21/n 1 | 11.089; 21.075; 12.128 90; 97.24; 90 | 2811.7 | Yang, Yanyan; Liu, Hongxu; Peng, Cheng; Wu, Jie; Zhang, Jingyi; Qiao, Yan; Wang, Xiao-Na; Chang, Junbiao AlCl<sub>3</sub>-Catalyzed Annulations of Ynamides Involving a Torquoselective Process for the Simultaneous Control of Central and Axial Chirality. Organic letters, 2016, 18, 5022-5025 |
| 1555787 | CIF | C32 H29 N O6 S | P 1 21/c 1 | 11.544; 14.011; 17.128 90; 99.02; 90 | 2736.1 | Yang, Yanyan; Liu, Hongxu; Peng, Cheng; Wu, Jie; Zhang, Jingyi; Qiao, Yan; Wang, Xiao-Na; Chang, Junbiao AlCl<sub>3</sub>-Catalyzed Annulations of Ynamides Involving a Torquoselective Process for the Simultaneous Control of Central and Axial Chirality. Organic letters, 2016, 18, 5022-5025 |
| 1555788 | CIF | C31 H27 N O6 S | P -1 | 9.6744; 11.557; 12.09 86.67; 80.45; 87.22 | 1329.7 | Yang, Yanyan; Liu, Hongxu; Peng, Cheng; Wu, Jie; Zhang, Jingyi; Qiao, Yan; Wang, Xiao-Na; Chang, Junbiao AlCl<sub>3</sub>-Catalyzed Annulations of Ynamides Involving a Torquoselective Process for the Simultaneous Control of Central and Axial Chirality. Organic letters, 2016, 18, 5022-5025 |
| 1555789 | CIF | C74 H18 F30 N8 | P 1 21/n 1 | 17.864; 23.111; 18.348 90; 110.537; 90 | 7094 | Kong, Jiahui; Zhang, Qiong; Savage, Mathew; Li, Minzhi; Li, Xin; Yang, Sihai; Liang, Xu; Zhu, Weihua; Ågren, Hans; Xie, Yongshu Tetra- and Octapyrroles Synthesized from Confusion and Fusion Approaches. Organic letters, 2016, 18, 5046-5049 |
| 1555790 | CIF | C40 H18 F15 N5 O | P 1 21/n 1 | 16.2619; 30.2509; 10.0784 90; 133.451; 90 | 3599.3 | Kong, Jiahui; Zhang, Qiong; Savage, Mathew; Li, Minzhi; Li, Xin; Yang, Sihai; Liang, Xu; Zhu, Weihua; Ågren, Hans; Xie, Yongshu Tetra- and Octapyrroles Synthesized from Confusion and Fusion Approaches. Organic letters, 2016, 18, 5046-5049 |
| 1555791 | CIF | C43 H19 Cl2 F15 N4 Ni O2 | P -1 | 12.7733; 12.9992; 14.5801 95.103; 107.136; 114.829 | 2035.5 | Kong, Jiahui; Zhang, Qiong; Savage, Mathew; Li, Minzhi; Li, Xin; Yang, Sihai; Liang, Xu; Zhu, Weihua; Ågren, Hans; Xie, Yongshu Tetra- and Octapyrroles Synthesized from Confusion and Fusion Approaches. Organic letters, 2016, 18, 5046-5049 |
| 1555792 | CIF | C30 H24 N2 O4 S2 | P 1 21/c 1 | 10.4528; 14.3902; 8.7251 90; 92.7628; 90 | 1310.89 | Seo, Boram; Kim, Ya Gob; Lee, Phil Ho Synthesis of Isothiazole via the Rhodium-Catalyzed Transannulation of 1,2,3-Thiadiazoles with Nitriles. Organic letters, 2016, 18, 5050-5053 |
| 1555793 | CIF | C30 H22 Br2 N2 O4 S2 | P 1 | 7.9207; 9.0758; 11.1924 80.79; 71.85; 65.087 | 693.02 | Seo, Boram; Kim, Ya Gob; Lee, Phil Ho Synthesis of Isothiazole via the Rhodium-Catalyzed Transannulation of 1,2,3-Thiadiazoles with Nitriles. Organic letters, 2016, 18, 5050-5053 |
| 1555794 | CIF | C18 H14 Br N O2 S | P -1 | 9.5374; 9.5911; 9.782 102.386; 108.954; 91.485 | 822.15 | Seo, Boram; Kim, Ya Gob; Lee, Phil Ho Synthesis of Isothiazole via the Rhodium-Catalyzed Transannulation of 1,2,3-Thiadiazoles with Nitriles. Organic letters, 2016, 18, 5050-5053 |
| 1555795 | CIF | C66 H62 Cl6 N4 | P 1 21/c 1 | 16.487; 19.2778; 18.1092 90; 101.874; 90 | 5632.5 | Zhu, Huangtianzhi; Shi, Bingbing; Chen, Kexian; Wei, Peifa; Xia, Danyu; Mondal, Julfikar Hassan; Huang, Feihe Cyclo[4]carbazole, an Iodide Anion Macrocyclic Receptor. Organic letters, 2016, 18, 5054-5057 |
| 1555796 | CIF | C64 H60 N4 | R -3 :H | 31.6291; 31.6291; 12.7824 90; 90; 120 | 11074.3 | Zhu, Huangtianzhi; Shi, Bingbing; Chen, Kexian; Wei, Peifa; Xia, Danyu; Mondal, Julfikar Hassan; Huang, Feihe Cyclo[4]carbazole, an Iodide Anion Macrocyclic Receptor. Organic letters, 2016, 18, 5054-5057 |
| 1555797 | CIF | C18 H15 N O3 | P 1 21/n 1 | 7.9712; 7.3926; 23.378 90; 94.406; 90 | 1373.5 | Jia, Feng-Cheng; Xu, Cheng; Zhou, Zhi-Wen; Cai, Qun; Wu, Yan-Dong; Wu, An-Xin Substrates as Electron-Donor Precursors: Synthesis of Naphtho-Fused Oxindoles via Benzannulation of 2-Halobenzaldehydes and Indolin-2-ones. Organic letters, 2016, 18, 5232-5235 |
| 1555798 | CIF | C17 H13 N O2 | P -1 | 8.338; 8.477; 9.528 93.456; 101.166; 104.331 | 636 | Jia, Feng-Cheng; Xu, Cheng; Zhou, Zhi-Wen; Cai, Qun; Wu, Yan-Dong; Wu, An-Xin Substrates as Electron-Donor Precursors: Synthesis of Naphtho-Fused Oxindoles via Benzannulation of 2-Halobenzaldehydes and Indolin-2-ones. Organic letters, 2016, 18, 5232-5235 |
| 1555799 | CIF | C15 H9 N O | P n a 21 | 14.933; 5.3922; 25.637 90; 90; 90 | 2064.3 | Jia, Feng-Cheng; Xu, Cheng; Zhou, Zhi-Wen; Cai, Qun; Wu, Yan-Dong; Wu, An-Xin Substrates as Electron-Donor Precursors: Synthesis of Naphtho-Fused Oxindoles via Benzannulation of 2-Halobenzaldehydes and Indolin-2-ones. Organic letters, 2016, 18, 5232-5235 |
| 1555800 | CIF | C17 H13 N O | P 21 21 21 | 7.2723; 12.1743; 13.9939 90; 90; 90 | 1239 | Jia, Feng-Cheng; Xu, Cheng; Zhou, Zhi-Wen; Cai, Qun; Wu, Yan-Dong; Wu, An-Xin Substrates as Electron-Donor Precursors: Synthesis of Naphtho-Fused Oxindoles via Benzannulation of 2-Halobenzaldehydes and Indolin-2-ones. Organic letters, 2016, 18, 5232-5235 |
| 1555801 | CIF | C21 H17 Br O2 | P 21 21 21 | 8.2974; 13.684; 15.775 90; 90; 90 | 1791.12 | Chen, Tao; Li, Yi-Fan; An, Yang; Zhang, Fu-Min Iron-Catalyzed α-Arylation of Deoxybenzoins with Arenes through an Oxidative Dehydrogenative Approach. Organic letters, 2016, 18, 4754-4757 |
| 1555802 | CIF | C21 H16 Cl2 O2 | P 1 21/n 1 | 10.0284; 17.8821; 10.2286 90; 98.735; 90 | 1813.01 | Chen, Tao; Li, Yi-Fan; An, Yang; Zhang, Fu-Min Iron-Catalyzed α-Arylation of Deoxybenzoins with Arenes through an Oxidative Dehydrogenative Approach. Organic letters, 2016, 18, 4754-4757 |
| 1555803 | CIF | C21 H16 Cl2 O2 | P -1 | 7.5712; 8.8981; 14.6818 76.585; 82.407; 74.099 | 922.81 | Chen, Tao; Li, Yi-Fan; An, Yang; Zhang, Fu-Min Iron-Catalyzed α-Arylation of Deoxybenzoins with Arenes through an Oxidative Dehydrogenative Approach. Organic letters, 2016, 18, 4754-4757 |
| 1555804 | CIF | C25 H18 N2 | P -1 | 10.098; 12.6554; 15.8728 103.793; 91.637; 111.127 | 1822.8 | Zhou, Tao; Wang, Yanwei; Li, Bin; Wang, Baiquan Rh(III)-Catalyzed Carbocyclization of 3-(Indolin-1-yl)-3-oxopropanenitriles with Alkynes and Alkenes through C-H Activation. Organic letters, 2016, 18, 5066-5069 |
| 1555805 | CIF | C20 H16 N2 | P 1 21/c 1 | 11.17; 16.077; 8.4209 90; 108.359; 90 | 1435.3 | Zhou, Tao; Wang, Yanwei; Li, Bin; Wang, Baiquan Rh(III)-Catalyzed Carbocyclization of 3-(Indolin-1-yl)-3-oxopropanenitriles with Alkynes and Alkenes through C-H Activation. Organic letters, 2016, 18, 5066-5069 |
| 1555806 | CIF | C25 H16 N2 | P 1 21/n 1 | 11.1107; 9.7397; 15.8289 90; 101.488; 90 | 1678.6 | Zhou, Tao; Wang, Yanwei; Li, Bin; Wang, Baiquan Rh(III)-Catalyzed Carbocyclization of 3-(Indolin-1-yl)-3-oxopropanenitriles with Alkynes and Alkenes through C-H Activation. Organic letters, 2016, 18, 5066-5069 |
| 1555807 | CIF | C19 H20 N2 O3 | P b c a | 10.6778; 15.1304; 20.376 90; 90; 90 | 3291.9 | Zhou, Tao; Wang, Yanwei; Li, Bin; Wang, Baiquan Rh(III)-Catalyzed Carbocyclization of 3-(Indolin-1-yl)-3-oxopropanenitriles with Alkynes and Alkenes through C-H Activation. Organic letters, 2016, 18, 5066-5069 |
| 1555808 | CIF | C24 H19 F N2 O3 | P 21 21 21 | 5.86821; 16.6995; 20.8172 90; 90; 90 | 2040.01 | Guo, Songsong; Liu, Xiaohua; Shen, Bin; Lin, Lili; Feng, Xiaoming Organocatalytic Asymmetric Cascade Reaction of 2-Hydroxyphenyl-Substituted Enones and Isocyanates To Construct 1,3-Benzoxazin-2-ones. Organic letters, 2016, 18, 5070-5073 |
| 1555809 | CIF | C23 H22 Cl N O3 S | P -1 | 12.179; 12.639; 15.612 95.437; 101.771; 115.319 | 2081.2 | Yabuuchi, Yuto; Kuzuguchi, Takeo; Yoshimura, Tomoyuki; Matsuo, Jun-Ichi Synthesis of α-Halo-γ-hydroxyenamides by Titanium Tetrahalide Mediated Addition of Aldehydes or Ketones to Ynamides. Organic letters, 2016, 18, 4951-4953 |
| 1555810 | CIF | C17 H18 Cl N O2 S | C 1 2/c 1 | 30.1678; 8.0311; 14.2794 90; 100.975; 90 | 3396.4 | Yabuuchi, Yuto; Kuzuguchi, Takeo; Yoshimura, Tomoyuki; Matsuo, Jun-Ichi Synthesis of α-Halo-γ-hydroxyenamides by Titanium Tetrahalide Mediated Addition of Aldehydes or Ketones to Ynamides. Organic letters, 2016, 18, 4951-4953 |
| 1555811 | CIF | C35 H31 N7 | P 1 21/c 1 | 19.24; 21.296; 14.917 90; 111.847; 90 | 5673 | Liu, Yang; Long, Chao; Zhao, Liang; Wang, Mei-Xiang Functionalization of Azacalixaromatics by Cu(II)-Catalyzed Oxidative Cross-Coupling Reaction between the Arene C-H Bond and Boronic Acids. Organic letters, 2016, 18, 5078-5081 |
| 1555812 | CIF | C35 H31 N7 | P 1 21/c 1 | 17.296; 10.5965; 15.8781 90; 101.794; 90 | 2848.7 | Liu, Yang; Long, Chao; Zhao, Liang; Wang, Mei-Xiang Functionalization of Azacalixaromatics by Cu(II)-Catalyzed Oxidative Cross-Coupling Reaction between the Arene C-H Bond and Boronic Acids. Organic letters, 2016, 18, 5078-5081 |
| 1555813 | CIF | C27 H23 N O4 S | P 1 21/n 1 | 9.3674; 22.177; 11.7 90; 106.835; 90 | 2326.4 | Guo, Songjin; Yuan, Kai; Gu, Meng; Lin, Aijun; Yao, Hequan Rh(III)-Catalyzed Cascade Annulation/C-H Activation of o-Ethynylanilines with Diazo Compounds: One-Pot Synthesis of Benzo[a]carbazoles via 1,4-Rhodium Migration. Organic letters, 2016, 18, 5236-5239 |
| 1555814 | CIF | C27 H24 O S2 | P -1 | 9.7091; 10.2062; 12.3 79.629; 69.436; 72.515 | 1084.7 | Liang, Yongping; Lai, Junshan; Liu, Teng; Tang, Shouchu Direct Regioselective [3 + 2]-Cyclization Reactions of Ambivalent Electrophilic/Nucleophilic β-Chlorovinyl Dithianes: Access to Cyclopentene Derivatives. Organic letters, 2016, 18, 5086-5089 |
| 1555815 | CIF | C27 H24 O S2 | P 1 21/n 1 | 15.4129; 9.30538; 15.704 90; 99.233; 90 | 2223.13 | Liang, Yongping; Lai, Junshan; Liu, Teng; Tang, Shouchu Direct Regioselective [3 + 2]-Cyclization Reactions of Ambivalent Electrophilic/Nucleophilic β-Chlorovinyl Dithianes: Access to Cyclopentene Derivatives. Organic letters, 2016, 18, 5086-5089 |
| 1555816 | CIF | C20 H17 Cl O4 | P 1 21/c 1 | 6.2163; 23.306; 11.8875 90; 96.96; 90 | 1709.5 | Zhang, Ming-Liang; Wu, Zhi-Jun; Zhao, Jian-Qiang; Luo, Yuan; Xu, Xiao-Ying; Zhang, Xiao-Mei; Yuan, Wei-Cheng Michael Addition-Lactonization of Arylacetyl Phosphonate to β,γ-Unsaturated α-Keto Esters for the Synthesis of Chiral syn-3,4-Dihydropyranones and 5,6-Dihydropyranones. Organic letters, 2016, 18, 5110-5113 |
| 1555817 | CIF | C19 H15 Br O4 | P 21 21 21 | 6.86; 10.8272; 22.448 90; 90; 90 | 1667.3 | Zhang, Ming-Liang; Wu, Zhi-Jun; Zhao, Jian-Qiang; Luo, Yuan; Xu, Xiao-Ying; Zhang, Xiao-Mei; Yuan, Wei-Cheng Michael Addition-Lactonization of Arylacetyl Phosphonate to β,γ-Unsaturated α-Keto Esters for the Synthesis of Chiral syn-3,4-Dihydropyranones and 5,6-Dihydropyranones. Organic letters, 2016, 18, 5110-5113 |
| 1555818 | CIF | C29 H23 O2 P Se | P 2 21 21 | 7.4297; 13.2923; 23.557 90; 90; 90 | 2326.4 | Maekawa, Yuuki; Maruyama, Toshifumi; Murai, Toshiaki Sequential Deprotonation-Alkylation of Binaphthyloxy-Substituted Phosphonochalcogenoates: Chiral Tri- and Tetrasubstituted Carbon Centers Adjacent to a Phosphorus Atom. Organic letters, 2016, 18, 5264-5267 |
| 1555819 | CIF | C30 H25 O2 P Se | P 21 21 21 | 7.48; 16.779; 19.319 90; 90; 90 | 2424.7 | Maekawa, Yuuki; Maruyama, Toshifumi; Murai, Toshiaki Sequential Deprotonation-Alkylation of Binaphthyloxy-Substituted Phosphonochalcogenoates: Chiral Tri- and Tetrasubstituted Carbon Centers Adjacent to a Phosphorus Atom. Organic letters, 2016, 18, 5264-5267 |
| 1555820 | CIF | C36 H27 O4 P Se | P 21 21 21 | 11.8545; 15.6874; 16.0313 90; 90; 90 | 2981.3 | Maekawa, Yuuki; Maruyama, Toshifumi; Murai, Toshiaki Sequential Deprotonation-Alkylation of Binaphthyloxy-Substituted Phosphonochalcogenoates: Chiral Tri- and Tetrasubstituted Carbon Centers Adjacent to a Phosphorus Atom. Organic letters, 2016, 18, 5264-5267 |
| 1555821 | CIF | C21 H22 O5 | P 1 21 1 | 8.4714; 6.2472; 17.1326 90; 101.606; 90 | 888.16 | Akula, Ramulu; Guiry, Patrick J. Enantioselective Synthesis of α-Allyl-α-aryldihydrocoumarins and 3-Isochromanones via Pd-Catalyzed Decarboxylative Asymmetric Allylic Alkylation. Organic letters, 2016, 18, 5472-5475 |
| 1555822 | CIF | C21 H18 O2 | P b c a | 7.5079; 14.0053; 29.564 90; 90; 90 | 3108.7 | Li, Deng Yuan; Jiang, Liang Liang; Chen, Shuang; Huang, Zheng Lu; Dang, Li; Wu, Xin Yan; Liu, Pei Nian Cascade Reaction of Alkynols and 7-Oxabenzonorbornadienes Involving Transient Hemiketal Group Directed C-H Activation and Synergistic Rh<sup>III</sup>/Sc<sup>III</sup> Catalysis. Organic letters, 2016, 18, 5134-5137 |
| 1555823 | CIF | C23 H21 Br2 N2 O | P 1 21/c 1 | 16.6039; 12.5136; 9.0084 90; 101.188; 90 | 1836.1 | Lin, Dongqing; Wei, Ying; Ou, Changjin; Huang, Hao; Xie, Linghai; Tang, Lei; Huang, Wei Carbon Cationic Relay via Superelectrophiles: Synthesis of Spiro-diazafluorenes. Organic letters, 2016, 18, 6220-6223 |
| 1555824 | CIF | C27 H28 O9 S | P -1 | 9.7672; 11.7742; 24.7073 101.224; 93.188; 112.05 | 2557.16 | Huang, Lin; Ye, Liu; Li, Xiao-Hua; Li, Zhong-Liang; Lin, Jin-Shun; Liu, Xin-Yuan Stereoselective Radical Cyclization Cascades Triggered by Addition of Diverse Radicals to Alkynes To Construct 6(5)-6-5 Fused Rings. Organic letters, 2016, 18, 5284-5287 |
| 1555825 | CIF | C16 H10 Br F3 N2 O | P -1 | 6.9696; 7.0783; 16.56 101.962; 93.626; 94.073 | 794.6 | Huang, Lin; Ye, Liu; Li, Xiao-Hua; Li, Zhong-Liang; Lin, Jin-Shun; Liu, Xin-Yuan Stereoselective Radical Cyclization Cascades Triggered by Addition of Diverse Radicals to Alkynes To Construct 6(5)-6-5 Fused Rings. Organic letters, 2016, 18, 5284-5287 |
| 1555826 | CIF | C18 H14 O3 | P 1 | 7.6607; 9.2315; 11.127 72.019; 79.887; 74.428 | 717.29 | Zhu, Gongming; Bao, Guangjun; Li, Yiping; Yang, Junxian; Sun, Wangsheng; Li, Jing; Hong, Liang; Wang, Rui Chiral Phosphoric Acid Catalyzed Asymmetric Oxidative Dearomatization of Naphthols with Quinones. Organic letters, 2016, 18, 5288-5291 |
| 1555827 | CIF | C23 H15 N O | P 1 21/n 1 | 8.542; 10.786; 18.502 90; 102.652; 90 | 1663.3 | Zhang, Fangfang; Qin, Zhengchen; Kong, Lingkai; Zhao, Yulei; Liu, Yuanyuan; Li, Yanzhong Metal/Benzoyl Peroxide (BPO)-Controlled Chemoselective Cycloisomerization of (o-Alkynyl)phenyl Enaminones: Synthesis of α-Naphthylamines and Indeno[1,2-c]pyrrolones. Organic letters, 2016, 18, 5150-5153 |
| 1555828 | CIF | C23 H17 N O | P -1 | 8.369; 9.476; 11.907 108.133; 106.771; 92.352 | 850.3 | Zhang, Fangfang; Qin, Zhengchen; Kong, Lingkai; Zhao, Yulei; Liu, Yuanyuan; Li, Yanzhong Metal/Benzoyl Peroxide (BPO)-Controlled Chemoselective Cycloisomerization of (o-Alkynyl)phenyl Enaminones: Synthesis of α-Naphthylamines and Indeno[1,2-c]pyrrolones. Organic letters, 2016, 18, 5150-5153 |
| 1555829 | CIF | C18 H14 N2 O4 | C 1 c 1 | 5.5545; 22.3478; 25.462 90; 94.477; 90 | 3151 | Meng, Ling-Hong; Wang, Chen-Yin; Mándi, Attila; Li, Xiao-Ming; Hu, Xue-Yi; Kassack, Matthias U.; Kurtán, Tibor; Wang, Bin-Gui Three Diketopiperazine Alkaloids with Spirocyclic Skeletons and One Bisthiodiketopiperazine Derivative from the Mangrove-Derived Endophytic Fungus Penicillium brocae MA-231. Organic letters, 2016, 18, 5304-5307 |
| 1555830 | CIF | C18 H20 O7 | P 1 21 1 | 6.7535; 10.0644; 12.3488 90; 91.205; 90 | 839.16 | Shi, Yunlong; Pierce, Joshua G. Stereocontrolled Synthesis of (+)-Plagiogyrin A. Organic letters, 2016, 18, 5308-5311 |
| 1555831 | CIF | C18 H20 O7 | P -1 | 8.8256; 9.3741; 10.7509 69.044; 81.513; 81.953 | 817.85 | Shi, Yunlong; Pierce, Joshua G. Stereocontrolled Synthesis of (+)-Plagiogyrin A. Organic letters, 2016, 18, 5308-5311 |
| 1555832 | CIF | C25 H30 N2 O9 | P -1 | 9.4188; 11.1969; 12.4356 101.95; 109.822; 95.373 | 1187.75 | Dwight, Stephen J.; Levin, Sergiy Scalable Regioselective Synthesis of Rhodamine Dyes. Organic letters, 2016, 18, 5316-5319 |
| 1555833 | CIF | C22 H21 N O5 | P -1 | 8.5998; 9.2091; 13.2372 84.15; 72.472; 64.512 | 901.91 | Dwight, Stephen J.; Levin, Sergiy Scalable Regioselective Synthesis of Rhodamine Dyes. Organic letters, 2016, 18, 5316-5319 |
| 1555834 | CIF | C9 H6 O5 | P 1 c 1 | 7.26017; 9.48057; 11.4368 90; 91.943; 90 | 786.75 | Dwight, Stephen J.; Levin, Sergiy Scalable Regioselective Synthesis of Rhodamine Dyes. Organic letters, 2016, 18, 5316-5319 |
| 1555835 | CIF | C15 H21 N O5 | P -1 | 8.8765; 9.1065; 9.7523 96.026; 90.185; 110.137 | 735.38 | Dwight, Stephen J.; Levin, Sergiy Scalable Regioselective Synthesis of Rhodamine Dyes. Organic letters, 2016, 18, 5316-5319 |
| 1555836 | CIF | C8 H5 Cl O3 | C 1 2/c 1 | 12.8414; 7.46056; 15.3814 90; 101.17; 90 | 1445.69 | Dwight, Stephen J.; Levin, Sergiy Scalable Regioselective Synthesis of Rhodamine Dyes. Organic letters, 2016, 18, 5316-5319 |
| 1555837 | CIF | C35 H34 N2 O5 | P 1 21/n 1 | 9.36155; 12.6426; 22.9131 90; 90.3246; 90 | 2711.82 | Dwight, Stephen J.; Levin, Sergiy Scalable Regioselective Synthesis of Rhodamine Dyes. Organic letters, 2016, 18, 5316-5319 |
| 1555838 | CIF | C34 H33 Cl N2 O3 | P 21 21 21 | 7.61287; 18.37433; 18.9503 90; 90; 90 | 2650.79 | Dwight, Stephen J.; Levin, Sergiy Scalable Regioselective Synthesis of Rhodamine Dyes. Organic letters, 2016, 18, 5316-5319 |
| 1555839 | CIF | C21 H20 Cl N O3 | P -1 | 8.3659; 8.5097; 13.3207 108.425; 106.74; 90.498 | 856.37 | Dwight, Stephen J.; Levin, Sergiy Scalable Regioselective Synthesis of Rhodamine Dyes. Organic letters, 2016, 18, 5316-5319 |
| 1555840 | CIF | C35 H40 N2 O8 | P -1 | 9.6296; 11.8041; 14.0277 96.799; 105.982; 92.907 | 1516.29 | Dwight, Stephen J.; Levin, Sergiy Scalable Regioselective Synthesis of Rhodamine Dyes. Organic letters, 2016, 18, 5316-5319 |
| 1555841 | CIF | C12 H13 N2 O S | P 1 21/c 1 | 5.8328; 14.6676; 14.1401 90; 106.475; 90 | 1160.06 | Andeme Edzang, Judicaelle; Chen, Zhongrui; Audi, Hassib; Canard, Gabriel; Siri, Olivier Transamination at the Crossroad of the One-Pot Synthesis of N-Substituted Quinonediimines and C-Substituted Benzobisimidazoles. Organic letters, 2016, 18, 5340-5343 |
| 1555842 | CIF | C11 H20 N2 | P -1 | 6.5009; 8.0222; 11.3792 85.438; 77.389; 72.879 | 553.39 | Andeme Edzang, Judicaelle; Chen, Zhongrui; Audi, Hassib; Canard, Gabriel; Siri, Olivier Transamination at the Crossroad of the One-Pot Synthesis of N-Substituted Quinonediimines and C-Substituted Benzobisimidazoles. Organic letters, 2016, 18, 5340-5343 |
| 1555843 | CIF | C25 H24 O4 | P 1 21/n 1 | 8.8495; 15.8052; 14.3121 90; 95.864; 90 | 1991.3 | Gratia, Synthia; Mosesohn, Kathryn; Diver, Steven T. Highly Selective Ring Expansion of Bicyclo[3.1.0]hexenes. Organic letters, 2016, 18, 5320-5323 |
| 1555844 | CIF | C21 H22 N2 | P -1 | 8.8501; 9.6086; 10.7805 74.645; 86.219; 69.215 | 826.09 | Song, Runzhe; Han, Zhaomeng; He, Qiuqin; Fan, Renhua Amine-Mediated Transimination and Aromatization-Triggered Domino Reaction in the Synthesis of Polyfunctionalized 4-Aminoquinolines. Organic letters, 2016, 18, 5328-5331 |
| 1555845 | CIF | C14 H16 O2 | P 1 21/n 1 | 8.5881; 15.4507; 8.7345 90; 99.603; 90 | 1142.76 | Peng, Yu; Xiao, Jian; Xu, Xiao-Bo; Duan, Shu-Ming; Ren, Li; Shao, Yong-Liang; Wang, Ya-Wen Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization. Organic letters, 2016, 18, 5170-5173 |
| 1555846 | CIF | C22 H22 O7 | P c a 21 | 15.8269; 5.82087; 20.8138 90; 90; 90 | 1917.5 | Peng, Yu; Xiao, Jian; Xu, Xiao-Bo; Duan, Shu-Ming; Ren, Li; Shao, Yong-Liang; Wang, Ya-Wen Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization. Organic letters, 2016, 18, 5170-5173 |
| 1555847 | CIF | C13 H14 O2 | P 1 21/n 1 | 6.8052; 10.2396; 15.216 90; 100.317; 90 | 1043.15 | Peng, Yu; Xiao, Jian; Xu, Xiao-Bo; Duan, Shu-Ming; Ren, Li; Shao, Yong-Liang; Wang, Ya-Wen Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization. Organic letters, 2016, 18, 5170-5173 |
| 1555848 | CIF | C14 H14 O2 | P b c a | 14.9062; 8.6079; 17.2918 90; 90; 90 | 2218.7 | Peng, Yu; Xiao, Jian; Xu, Xiao-Bo; Duan, Shu-Ming; Ren, Li; Shao, Yong-Liang; Wang, Ya-Wen Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization. Organic letters, 2016, 18, 5170-5173 |
| 1555849 | CIF | C16 H22 O4 | P 1 21/c 1 | 25.983; 5.7576; 10.4224 90; 100.35; 90 | 1533.8 | Peng, Yu; Xiao, Jian; Xu, Xiao-Bo; Duan, Shu-Ming; Ren, Li; Shao, Yong-Liang; Wang, Ya-Wen Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization. Organic letters, 2016, 18, 5170-5173 |
| 1555850 | CIF | C12 H12 O2 | P 1 21/n 1 | 8.27; 8.534; 13.743 90; 90.047; 90 | 969.9 | Peng, Yu; Xiao, Jian; Xu, Xiao-Bo; Duan, Shu-Ming; Ren, Li; Shao, Yong-Liang; Wang, Ya-Wen Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization. Organic letters, 2016, 18, 5170-5173 |
| 1555851 | CIF | C15 H15 N O3 | P -1 | 7.236; 8.5114; 11.77 107.206; 104.236; 99.256 | 649.5 | Lanke, Veeranjaneyulu; Bettadapur, Kiran R.; Prabhu, Kandikere Ramaiah Electronic Nature of Ketone Directing Group as a Key To Control C-2 vs C-4 Alkenylation of Indoles. Organic letters, 2016, 18, 5496-5499 |
| 1555852 | CIF | C15 H12 F3 N O3 | C 1 c 1 | 28.703; 13.0666; 8.1548 90; 106.279; 90 | 2935.8 | Lanke, Veeranjaneyulu; Bettadapur, Kiran R.; Prabhu, Kandikere Ramaiah Electronic Nature of Ketone Directing Group as a Key To Control C-2 vs C-4 Alkenylation of Indoles. Organic letters, 2016, 18, 5496-5499 |
| 1555853 | CIF | C23 H23 N O7 S | P 1 21/c 1 | 12.0449; 17.559; 11.278 90; 105.674; 90 | 2296.56 | Yuan, Hao; Gong, Jianxian; Yang, Zhen Stereoselective Synthesis of Oxabicyclo[2.2.1]heptenes via a Tandem Dirhodium(II)-Catalyzed Triazole Denitrogenation and [3 + 2] Cycloaddition. Organic letters, 2016, 18, 5500-5503 |
| 1555854 | CIF | C28 H31 N O7 S | P 1 21/c 1 | 16.125; 19.416; 9.015 90; 102.099; 90 | 2759.7 | Yuan, Hao; Gong, Jianxian; Yang, Zhen Stereoselective Synthesis of Oxabicyclo[2.2.1]heptenes via a Tandem Dirhodium(II)-Catalyzed Triazole Denitrogenation and [3 + 2] Cycloaddition. Organic letters, 2016, 18, 5500-5503 |
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