Crystallography Open Database
Search results
Result: there are 895 entries in the selection
Switch to the old layout of the pageDownload all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)
Searching journal of publication like 'Organic letters' volume of publication is 17
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
---|---|---|---|---|---|---|
1518687 | CIF | C63 H70 N4 O16 | P -1 | 11.12; 14.029; 20.02 108.726; 98.537; 94.981 | 2894.8 | Tominaga, Masahide; Kunitomi, Nobuto; Katagiri, Kosuke; Itoh, Tsutomu Adamantane-based oxacyclophanes containing pyrazines: synthesis, crystal structure, and self-assembly behavior. Organic letters, 2015, 17, 786-789 |
1518712 | CIF | C21 H28 O3 | P 21 21 21 | 6.0078; 15.1366; 20.0221 90; 90; 90 | 1820.76 | Parr, Brendan T.; Davies, Huw M. L. Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence. Organic letters, 2015, 17, 794-797 |
1518713 | CIF | C23 H27 F3 O3 | P 21 21 21 | 6.2097; 14.9142; 23.193 90; 90; 90 | 2147.97 | Parr, Brendan T.; Davies, Huw M. L. Stereoselective synthesis of highly substituted cyclohexanes by a rhodium-carbene initiated domino sequence. Organic letters, 2015, 17, 794-797 |
1518718 | CIF | C18 H26 O4 Si | P b c a | 16.759; 7.4334; 30.141 90; 90; 90 | 3754.9 | Xu, Xinfang; Wang, Xiangbo; Zavalij, Peter Y.; Doyle, Michael P. Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade. Organic letters, 2015, 17, 790-793 |
1518719 | CIF | C18 H26 O4 Si | P -1 | 6.1239; 16.8945; 17.8873 91.468; 95.3024; 90.184 | 1842.1 | Xu, Xinfang; Wang, Xiangbo; Zavalij, Peter Y.; Doyle, Michael P. Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade. Organic letters, 2015, 17, 790-793 |
1518723 | CIF | C32 H28 O4 Si | P -1 | 7.0418; 10.4998; 17.4226 93.591; 96.204; 103.663 | 1239.21 | Pogula, Vedamayee D.; Wang, Tao; Hoye, Thomas R. Intramolecular [4 + 2] Trapping of a Hexadehydro-Diels-Alder (HDDA) Benzyne by Tethered Arenes. Organic letters, 2015, 17, 856-859 |
1518724 | CIF | C31 H28 O4 Si | P 1 21/n 1 | 14.0146; 10.5314; 16.6752 90; 100.775; 90 | 2417.8 | Pogula, Vedamayee D.; Wang, Tao; Hoye, Thomas R. Intramolecular [4 + 2] Trapping of a Hexadehydro-Diels-Alder (HDDA) Benzyne by Tethered Arenes. Organic letters, 2015, 17, 856-859 |
1518725 | CIF | C18 H12 F N O3 | P 1 21/c 1 | 3.798; 11.416; 31.2 90; 90.82; 90 | 1353 | Qian, Jinlong; Yi, Wenbin; Huang, Xin; Miao, Yongbo; Zhang, Junkai; Cai, Chun; Zhang, Wei One-pot synthesis of 3,5-disubstituted and polysubstituted phenols from acyclic precursors. Organic letters, 2015, 17, 1090-1093 |
1518726 | CIF | C22 H16 F4 O3 | P -1 | 7.668; 11.45; 11.497 97.96; 98.584; 103.944 | 952.6 | Qian, Jinlong; Yi, Wenbin; Huang, Xin; Miao, Yongbo; Zhang, Junkai; Cai, Chun; Zhang, Wei One-pot synthesis of 3,5-disubstituted and polysubstituted phenols from acyclic precursors. Organic letters, 2015, 17, 1090-1093 |
1518747 | CIF | C14 H9 Cl N4 O2 | P -1 | 11.31; 13.792; 13.982 93.902; 90.56; 112.233 | 2012.7 | Chen, Yunfeng; Nie, Gang; Zhang, Qi; Ma, Shan; Li, Huan; Hu, Qinquan Copper-Catalyzed [3 + 2] Cycloaddition/Oxidation Reactions between Nitro-olefins and Organic Azides: Highly Regioselective Synthesis of NO2-Substituted 1,2,3-Triazoles. Organic letters, 2015, 17, 1118-1121 |
1518748 | CIF | C15 H11 Br N4 O2 | P b c a | 10.784; 9.6655; 28.858 90; 90; 90 | 3007.9 | Chen, Yunfeng; Nie, Gang; Zhang, Qi; Ma, Shan; Li, Huan; Hu, Qinquan Copper-Catalyzed [3 + 2] Cycloaddition/Oxidation Reactions between Nitro-olefins and Organic Azides: Highly Regioselective Synthesis of NO2-Substituted 1,2,3-Triazoles. Organic letters, 2015, 17, 1118-1121 |
1518770 | CIF | C20 H16 Cl4 N2 | P b c a | 11.2813; 14.1148; 24.5832 90; 90; 90 | 3914.5 | Zhan, Ming; Zhang, Shaoguang; Huang, Zhe; Xi, Zhenfeng Synthesis of α,α,α',α'-Tetrachloro-Δ(1)-bipyrrolines and 4,8-Dichloro-2,6-diazasemibuvallenes. Organic letters, 2015, 17, 1026-1029 |
1518771 | CIF | C18 H26 Cl2 N2 | P -1 | 9.3474; 9.8657; 12.3923 66.695; 69.579; 62.115 | 908.59 | Zhan, Ming; Zhang, Shaoguang; Huang, Zhe; Xi, Zhenfeng Synthesis of α,α,α',α'-Tetrachloro-Δ(1)-bipyrrolines and 4,8-Dichloro-2,6-diazasemibuvallenes. Organic letters, 2015, 17, 1026-1029 |
1518772 | CIF | C28 H23 Br Cl3 N O2 | P 21 21 21 | 9.6557; 10.7366; 25.0366 90; 90; 90 | 2595.53 | Saha, Satyajit; Schneider, Christoph Directing Group Assisted Nucleophilic Substitution of Propargylic Alcohols via o-Quinone Methide Intermediates: Brønsted Acid Catalyzed, Highly Enantio- and Diastereoselective Synthesis of 7-Alkynyl-12a-acetamido-Substituted Benzoxanthenes. Organic letters, 2015, 17, 648-651 |
1518773 | CIF | C26 H21 N O2 S | P 21 21 21 | 7.3516; 9.5635; 29.4896 90; 90; 90 | 2073.33 | Saha, Satyajit; Schneider, Christoph Directing Group Assisted Nucleophilic Substitution of Propargylic Alcohols via o-Quinone Methide Intermediates: Brønsted Acid Catalyzed, Highly Enantio- and Diastereoselective Synthesis of 7-Alkynyl-12a-acetamido-Substituted Benzoxanthenes. Organic letters, 2015, 17, 648-651 |
1518783 | CIF | C23 H16 N2 | P 1 21/c 1 | 14.9264; 8.5389; 13.3223 90; 96.518; 90 | 1687.02 | Zhang, Wei; Wei, Jun; Fu, Shaomin; Lin, Dongen; Jiang, Huanfeng; Zeng, Wei Highly Stereoselective Ruthenium(II)-Catalyzed Direct C2-syn-Alkenylation of Indoles with Alkynes. Organic letters, 2015, 17, 1349-1352 |
1518820 | CIF | C23 H17 N O | P 1 | 9.9575; 10.7208; 16.4862 91.531; 105.749; 104.208 | 1633.82 | Yang, Xiao-Fei; Hu, Xu-Hong; Loh, Teck-Peng Expedient Synthesis of Pyrroloquinolinones by Rh-Catalyzed Annulation of N-Carbamoyl Indolines with Alkynes through a Directed C-H Functionalization/C-N Cleavage Sequence. Organic letters, 2015, 17, 1481-1484 |
1518842 | CIF | C15 H13 F O2 S | P 21 21 21 | 5.9536; 7.269; 31.978 90; 90; 90 | 1383.9 | Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones. Organic letters, 2015, 17, 1692-1695 |
1518936 | CIF | C18 H24 F N O4 S | P 1 21/c 1 | 9.8882; 17.552; 11.4151 90; 103.067; 90 | 1929.9 | Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K. Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery. Organic letters, 2015, 17, 1922-1925 |
1518937 | CIF | C13 H15 N O4 S | P -1 | 6.7205; 8.781; 11.3856 103.22; 104.242; 92.033 | 630.98 | Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K. Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery. Organic letters, 2015, 17, 1922-1925 |
1518938 | CIF | C19 H28 N2 O4 S | P -1 | 10.0063; 10.3287; 10.8385 65.843; 70.701; 84.706 | 963.4 | Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K. Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery. Organic letters, 2015, 17, 1922-1925 |
1518939 | CIF | C15 H18 N2 S | P 1 21/c 1 | 10.8363; 14.406; 9.9733 90; 117.4; 90 | 1382.2 | Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K. Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery. Organic letters, 2015, 17, 1922-1925 |
1518940 | CIF | C15 H21 N O3 S | P 1 21/c 1 | 7.3226; 10.563; 18.9019 90; 92.929; 90 | 1460.13 | Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K. Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery. Organic letters, 2015, 17, 1922-1925 |
1518941 | CIF | C14 H19 N O3 S | P b c a | 8.4818; 10.9461; 30.035 90; 90; 90 | 2788.5 | Druzhenko, Tetiana; Denisenko, Olexandr; Kheylik, Yuri; Zozulya, Sergey; Shishkina, Svitlana S.; Tolmachev, Andrei; Mykhailiuk, Pavel K. Design, Synthesis, and Characterization of SO2-Containing Azabicyclo[3.n.1]alkanes: Promising Building Blocks for Drug Discovery. Organic letters, 2015, 17, 1922-1925 |
1518989 | CIF | C19 H12 Cl2 N2 | P 1 21/c 1 | 12.7382; 11.0562; 12.4976 90; 112.701; 90 | 1623.76 | Tiwari, Virendra Kumar; Kamal, Neha; Kapur, Manmohan Ruthenium-catalyzed heteroatom-directed regioselective C-h arylation of indoles using a removable tether. Organic letters, 2015, 17, 1766-1769 |
1518990 | CIF | C17 H17 O P Si | P c a 21 | 14.4427; 6.5207; 16.6673 90; 90; 90 | 1569.67 | Xu, Youzhi; Wang, Zhihua; Gan, Zhenjie; Xi, Qiuzhen; Duan, Zheng; Mathey, François Versatile synthesis of phospholides from open-chain precursors. Application to annelated pyrrole- and silole-phosphole rings. Organic letters, 2015, 17, 1732-1734 |
1518991 | CIF | C21 H17 F O2 S | P 1 21/n 1 | 12.402; 5.782; 24.377 90; 100.253; 90 | 1720.1 | Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones. Organic letters, 2015, 17, 1692-1695 |
1518992 | CIF | C16 H16 O2 S | P 21 21 21 | 5.7471; 8.0541; 31.351 90; 90; 90 | 1451.2 | Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones. Organic letters, 2015, 17, 1692-1695 |
1518993 | CIF | C21 H18 O2 S | P 1 21/n 1 | 12.3084; 5.8277; 24.345 90; 100.373; 90 | 1717.7 | Mao, Shuai; Gao, Ya-Ru; Zhu, Xue-Qing; Guo, Dong-Dong; Wang, Yong-Qiang Copper-catalyzed radical reaction of N-tosylhydrazones: stereoselective synthesis of (e)-vinyl sulfones. Organic letters, 2015, 17, 1692-1695 |
1518994 | CIF | C14 H17 N O3 S | C 1 2/c 1 | 25.7457; 5.8011; 19.0494 90; 98.23; 90 | 2815.79 | Cheng, Cungui; Liu, Shuiyou; Zhu, Gangguo Palladium-catalyzed cycloisomerization and aerobic oxidative cycloisomerization of homoallenyl amides: a facile and divergent approach to 2-aminofurans. Organic letters, 2015, 17, 1581-1584 |
1518995 | CIF | C15 H21 N O4 S | P b c n | 16.428; 13.329; 14.387 90; 90; 90 | 3150 | Zhu, Haitao; Chen, Pinhong; Liu, Guosheng Palladium-catalyzed intramolecular aminoacetoxylation of unactivated alkenes with hydrogen peroxide as oxidant. Organic letters, 2015, 17, 1485-1488 |
1518996 | CIF | C20 H20 N2 O3 | P 21 21 21 | 9.8991; 10.1513; 17.5003 90; 90; 90 | 1758.6 | Yetra, Santhivardhana Reddy; Mondal, Santigopal; Suresh, Eringathodi; Biju, Akkattu T. Enantioselective Synthesis of Functionalized Pyrazoles by NHC-Catalyzed Reaction of Pyrazolones with α,β-Unsaturated Aldehydes. Organic letters, 2015, 17, 1417-1420 |
1518997 | CIF | C11 H14 O3 | P n a 21 | 14.5121; 5.9558; 24.1332 90; 90; 90 | 2085.9 | Qin, Yan; Zhang, Long; Lv, Jian; Luo, Sanzhong; Cheng, Jin-Pei Bioinspired Organocatalytic Aerobic C-H Oxidation of Amines with an ortho-Quinone Catalyst. Organic letters, 2015, 17, 1469-1472 |
1518998 | CIF | C16 H14 O2 | P 21 21 21 | 8.477; 8.5847; 17.547 90; 90; 90 | 1276.94 | Jiang, Liyin; Jia, Tao; Wang, Min; Liao, Jian; Cao, Peng Pd-catalyzed enantioselective hydroalkoxylation of alkoxyallenes with phenol for construction of acyclic o,o-acetals. Organic letters, 2015, 17, 1070-1073 |
1518999 | CIF | C17 H13 F O3 S | P 1 21/n 1 | 9.2698; 11.0134; 15.0573 90; 105.111; 90 | 1484.08 | Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju Bi(OTf)3-Mediated Cycloisomerization of γ-Alkynyl Arylketones: Application to the Synthesis of Substituted Furans. Organic letters, 2015, 17, 1264-1267 |
1519496 | CIF | C22 H20 Br N | P 1 | 6.134; 7.123; 10.777 102.328; 106.299; 90.659 | 440.2 | Zhang, Zhenhua; Du, Haifeng Cis-selective and highly enantioselective hydrogenation of 2,3,4-trisubstituted quinolines. Organic letters, 2015, 17, 2816-2819 |
1519622 | CIF | C22 H18 Cl N O3 Pd | P 1 21/c 1 | 19.306; 4.5687; 22.128 90; 103.674; 90 | 1896.4 | Ren, Zhi; Schulz, Jonathan E.; Dong, Guangbin Catalytic Ortho-Acetoxylation of Masked Benzyl Alcohols via an Exo-Directing Mode. Organic letters, 2015, 17, 2696-2699 |
1519623 | CIF | C15 H10 I N O2 | C 1 c 1 | 24.877; 7.087; 7.92 90; 90.593; 90 | 1396.2 | Huang, Hai; Zhu, Xiaolin; He, Guangke; Liu, Qi; Fan, Junzhen; Zhu, Hongjun Controlled Synthesis of 1,3,5-Oxadiazin-2-ones and Oxazolones through Regioselective Iodocyclization of Ynamides. Organic letters, 2015, 17, 2510-2513 |
1519625 | CIF | C32 H30 B N | P 1 21/c 1 | 10.2671; 10.1236; 23.3329 90; 98.876; 90 | 2396.18 | Yang, Deng-Tao; Radtke, Julian; Mellerup, Soren K.; Yuan, Kang; Wang, Xiang; Wagner, Matthias; Wang, Suning One-Pot Synthesis of Brightly Fluorescent Mes2B-Functionalized Indolizine Derivatives via Cycloaddition Reactions. Organic letters, 2015, 17, 2486-2489 |
1519626 | CIF | C32 H32 B N | P 1 21/c 1 | 10.0993; 10.2609; 23.8794 90; 97.3582; 90 | 2454.19 | Yang, Deng-Tao; Radtke, Julian; Mellerup, Soren K.; Yuan, Kang; Wang, Xiang; Wagner, Matthias; Wang, Suning One-Pot Synthesis of Brightly Fluorescent Mes2B-Functionalized Indolizine Derivatives via Cycloaddition Reactions. Organic letters, 2015, 17, 2486-2489 |
1519627 | CIF | C38 H34 B N | P -1 | 8.8087; 11.1753; 16.1219 72.148; 78.052; 74.662 | 1443.04 | Yang, Deng-Tao; Radtke, Julian; Mellerup, Soren K.; Yuan, Kang; Wang, Xiang; Wagner, Matthias; Wang, Suning One-Pot Synthesis of Brightly Fluorescent Mes2B-Functionalized Indolizine Derivatives via Cycloaddition Reactions. Organic letters, 2015, 17, 2486-2489 |
1519628 | CIF | C102 H70 B4 O20 | C 1 2/c 1 | 30.624; 56.38; 22.177 90; 93.399; 90 | 38223 | Danjo, Hiroshi; Kidena, Yuki; Kawahata, Masatoshi; Sato, Hiroyasu; Katagiri, Kosuke; Miyazawa, Toshifumi; Yamaguchi, Kentaro Multilayered inclusion nanocycles of anionic spiroborates. Organic letters, 2015, 17, 2466-2469 |
1519629 | CIF | C21 H26 N2 O2 S | P 1 21/c 1 | 7.3915; 13.779; 19.135 90; 93.863; 90 | 1944.4 | Kumar, Yalla Kiran; Kumar, Gadi Ranjith; Reddy, Thota Jagadeshwar; Sridhar, Balasubramanian; Reddy, Maddi Sridhar Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion. Organic letters, 2015, 17, 2226-2229 |
1519630 | CIF | C16 H14 N2 O2 S | P 1 21/c 1 | 11.225; 13.361; 11.0143 90; 118.102; 90 | 1457.2 | Kumar, Yalla Kiran; Kumar, Gadi Ranjith; Reddy, Thota Jagadeshwar; Sridhar, Balasubramanian; Reddy, Maddi Sridhar Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion. Organic letters, 2015, 17, 2226-2229 |
1519631 | CIF | C17 H16 N2 O2 S | P 1 21/c 1 | 8.9148; 16.7339; 10.5655 90; 95.855; 90 | 1567.93 | Kumar, Yalla Kiran; Kumar, Gadi Ranjith; Reddy, Thota Jagadeshwar; Sridhar, Balasubramanian; Reddy, Maddi Sridhar Synthesis of 3-Sulfonylamino Quinolines from 1-(2-Aminophenyl) Propargyl Alcohols through a Ag(I)-Catalyzed Hydroamination, (2 + 3) Cycloaddition, and an Unusual Strain-Driven Ring Expansion. Organic letters, 2015, 17, 2226-2229 |
1519651 | CIF | C14 H15 F3 O4 S | P 1 21/n 1 | 5.4571; 34.89; 7.6271 90; 96.378; 90 | 1443.2 | Liu, Yafei; Shao, Xinxin; Zhang, Panpan; Lu, Long; Shen, Qilong Trifluoromethyl-substituted sulfonium ylide: rh-catalyzed carbenoid addition to trifluoromethylthioether. Organic letters, 2015, 17, 2752-2755 |
1519652 | CIF | C47 H59 N O5 | P n 21 a | 18.4589; 58.006; 11.59672 90; 90; 90 | 12416.9 | Slavík, Petr; Eigner, Václav; Lhoták, Pavel Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds. Organic letters, 2015, 17, 2788-2791 |
1519653 | CIF | C41 H46 O5 | C 1 2/c 1 | 34.9361; 10.48642; 26.842 90; 135.583; 90 | 6882.4 | Slavík, Petr; Eigner, Václav; Lhoták, Pavel Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds. Organic letters, 2015, 17, 2788-2791 |
1519654 | CIF | C48.5 H58 O6.5 | P 1 21 1 | 20.7243; 10.45113; 21.5504 90; 113.543; 90 | 4279.1 | Slavík, Petr; Eigner, Václav; Lhoták, Pavel Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds. Organic letters, 2015, 17, 2788-2791 |
1519655 | CIF | C20 H16 Br N O4 | C 1 c 1 | 14.0307; 8.5721; 15.203 90; 109.89; 90 | 1719.4 | Lin, Chao; Zhen, Le; Cheng, Yong; Du, Hong-Jin; Zhao, Hui; Wen, Xiaoan; Kong, Ling-Yi; Xu, Qing-Long; Sun, Hongbin Visible-light induced isoindoles formation to trigger intermolecular diels-alder reactions in the presence of air. Organic letters, 2015, 17, 2684-2687 |
1519656 | CIF | C25 H20 N2 O2 | P 1 21/c 1 | 13.373; 16.581; 8.8083 90; 93.638; 90 | 1949.2 | Lin, Chao; Zhen, Le; Cheng, Yong; Du, Hong-Jin; Zhao, Hui; Wen, Xiaoan; Kong, Ling-Yi; Xu, Qing-Long; Sun, Hongbin Visible-light induced isoindoles formation to trigger intermolecular diels-alder reactions in the presence of air. Organic letters, 2015, 17, 2684-2687 |
1519657 | CIF | C24 H28 Cl N O7 | P 1 21/n 1 | 10.5446; 9.5462; 24.575 90; 91.778; 90 | 2472.5 | Hu, Jiang-Lin; Wang, Lijia; Xu, Hao; Xie, Zuowei; Tang, Yong Highly diastereoselective and enantioselective formal [4 + 3] cycloaddition of donor-acceptor cyclobutanes with nitrones. Organic letters, 2015, 17, 2680-2683 |
1519658 | CIF | C28 H28 Br N O6 | P 21 21 21 | 10.409; 15.4718; 16.588 90; 90; 90 | 2671.4 | Hu, Jiang-Lin; Wang, Lijia; Xu, Hao; Xie, Zuowei; Tang, Yong Highly diastereoselective and enantioselective formal [4 + 3] cycloaddition of donor-acceptor cyclobutanes with nitrones. Organic letters, 2015, 17, 2680-2683 |
1519694 | CIF | C14 H11 N O4 S | P 1 21/c 1 | 5.7372; 21.0648; 10.9631 90; 94.428; 90 | 1321 | Singh, Rahul; Allam, Bharat Kumar; Singh, Neetu; Kumari, Kumkum; Singh, Satish Kumar; Singh, Krishna Nand A Direct Metal-Free Decarboxylative Sulfono Functionalization (DSF) of Cinnamic Acids to α,β-Unsaturated Phenyl Sulfones. Organic letters, 2015, 17, 2656-2659 |
1519695 | CIF | C23 H22 O2 | P 21 21 21 | 8.099; 13.445; 16.407 90; 90; 90 | 1786.6 | Mitra, Nirmal K.; Meudom, Rolande; Gorden, John D.; Merner, Bradley L. A non-cross-coupling approach to arene-bridged macrocycles: synthesis, structure, and direct, regioselective functionalization of a cycloparaphenylene fragment. Organic letters, 2015, 17, 2700-2703 |
1519696 | CIF | C13 H13 F O | P 21 21 21 | 6.1061; 18.8064; 27.8827 90; 90; 90 | 3201.88 | Witten, Michael R.; Jacobsen, Eric N. A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes. Organic letters, 2015, 17, 2772-2775 |
1519697 | CIF | C9 H10 Br F O | P 1 21 1 | 8.013; 5.1662; 10.972 90; 93.376; 90 | 453.4 | Witten, Michael R.; Jacobsen, Eric N. A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes. Organic letters, 2015, 17, 2772-2775 |
1519698 | CIF | C10 H13 F O | P 21 21 21 | 5.5342; 11.1421; 14.6505 90; 90; 90 | 903.39 | Witten, Michael R.; Jacobsen, Eric N. A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes. Organic letters, 2015, 17, 2772-2775 |
1519755 | CIF | C15 H16 O4 | P 1 21/c 1 | 7.4665; 21.583; 8.4033 90; 107.586; 90 | 1290.9 | Zhang, Xuxue; Dai, Wenpeng; Wu, Wei; Cao, Song Copper-Catalyzed Coupling Cyclization of gem-Difluoroalkenes with Activated Methylene Carbonyl Compounds: Facile Domino Access to Polysubstituted Furans. Organic letters, 2015, 17, 2708-2711 |
1519756 | CIF | C30 H42 O5 | P 1 21 1 | 7.3312; 12.6193; 14.4778 90; 98.847; 90 | 1323.47 | Zhao, Qian-Qian; Song, Qiu-Yan; Jiang, Kan; Li, Guang-Da; Wei, Wen-Jun; Li, Ya; Gao, Kun Spirochensilides A and B, Two New Rearranged Triterpenoids from Abies chensiensis. Organic letters, 2015, 17, 2760-2763 |
1519757 | CIF | C10 H7 Br Cl2 N2 O | P b c a | 12.6226; 12.3709; 14.1124 90; 90; 90 | 2203.7 | Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles. Organic letters, 2015, 17, 2856-2859 |
1519758 | CIF | C12 H12 Br2 N2 O | P 1 21/c 1 | 7.3945; 20.124; 17.43 90; 91.44; 90 | 2592.9 | Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles. Organic letters, 2015, 17, 2856-2859 |
1519759 | CIF | C11 H10 Br2 N2 | P 1 21/c 1 | 14.9133; 10.5056; 7.3297 90; 103.561; 90 | 1116.35 | Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles. Organic letters, 2015, 17, 2856-2859 |
1519760 | CIF | C11 H7 Cl2 F3 N2 O1.5 | P 1 21/c 1 | 7.501; 40.025; 16.7795 90; 94.664; 90 | 5021 | Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles. Organic letters, 2015, 17, 2856-2859 |
1519761 | CIF | C11 H9 Br2 F N2 | P b c a | 14.443; 7.5861; 21.306 90; 90; 90 | 2334.4 | Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles. Organic letters, 2015, 17, 2856-2859 |
1519848 | CIF | C12 H14 O3 | P 1 21/c 1 | 8.8887; 18.4179; 6.9957 90; 115.638; 90 | 1032.52 | Hassan, Ahmed H. E.; Lee, Jae Kyun; Pae, Ae Nim; Min, Sun-Joon; Cho, Yong Seo Synthesis of the Tricyclic Ring Structure of Daphnanes via Intramolecular [4 + 3] Cycloaddition/SmI2-Pinacol Coupling. Organic letters, 2015, 17, 2672-2675 |
1519849 | CIF | C12 H14 O3 | P 1 21/c 1 | 10.7308; 8.7467; 12.089 90; 109.485; 90 | 1069.68 | Hassan, Ahmed H. E.; Lee, Jae Kyun; Pae, Ae Nim; Min, Sun-Joon; Cho, Yong Seo Synthesis of the Tricyclic Ring Structure of Daphnanes via Intramolecular [4 + 3] Cycloaddition/SmI2-Pinacol Coupling. Organic letters, 2015, 17, 2672-2675 |
1519850 | CIF | C22 H16 Br N O2 | P 1 21/c 1 | 5.7399; 15.532; 20.365 90; 96.93; 90 | 1802.3 | Dhanasekaran, Sivasankaran; Kayet, Anirban; Suneja, Arun; Bisai, Vishnumaya; Singh, Vinod K. Unified Approach to Isoindolinones and THIQs via Lewis Acid Catalyzed Domino Mukaiyama-Mannich Lactamization/Alkylations: Application in the Synthesis of (±)-Homolaudanosine. Organic letters, 2015, 17, 2780-2783 |
1519851 | CIF | C16 H12 N4 | P 1 21/c 1 | 4.8624; 11.167; 23.437 90; 94.33; 90 | 1269 | Jia, Feng-Cheng; Xu, Cheng; Zhou, Zhi-Wen; Cai, Qun; Li, Deng-Kui; Wu, An-Xin Consecutive Cycloaddition/SNAr/Reduction/Cyclization/Oxidation Sequences: A Copper-Catalyzed Multicomponent Synthesis of Fused N-Heterocycles. Organic letters, 2015, 17, 2820-2823 |
1519923 | CIF | C21 H34 O3 | P 1 21 1 | 6.1791; 23.0423; 6.9392 90; 110.037; 90 | 928.21 | Hosseini, Abolfazl; Seidel, Daniel; Miska, Andreas; Schreiner, Peter R. Fluoride-assisted activation of calcium carbide: a simple method for the ethynylation of aldehydes and ketones. Organic letters, 2015, 17, 2808-2811 |
1519924 | CIF | C25 H21 Fe N3 | P 1 21/c 1 | 10.9392; 8.3314; 22.5089 90; 102.759; 90 | 2000.78 | Wei, Fang; Li, Haoyu; Song, Chuanling; Ma, Yudao; Zhou, Ling; Tung, Chen-Ho; Xu, Zhenghu Cu/Pd-Catalyzed, Three-Component Click Reaction of Azide, Alkyne, and Aryl Halide: One-Pot Strategy toward Trisubstituted Triazoles. Organic letters, 2015, 17, 2860-2863 |
1519998 | CIF | C20 H30 N0 O5 | P 21 21 21 | 7.0685; 15.143; 17.388 90; 90; 90 | 1861.2 | Annam, S Ch V Appa Rao; Ankireddy, Madhu; Sura, Madhu Babu; Ponnapalli, Mangala Gowri; Sarma, Akella V. S.; S, Jeelani Basha Epimeric Excolides from the Stems of Excoecaria agallocha and Structural Revision of Rhizophorin A. Organic letters, 2015, 17, 2840-2843 |
1519999 | CIF | C20 H28 O5 | P 1 21 1 | 9.4777; 7.3392; 13.4089 90; 91.432; 90 | 932.41 | Annam, S Ch V Appa Rao; Ankireddy, Madhu; Sura, Madhu Babu; Ponnapalli, Mangala Gowri; Sarma, Akella V. S.; S, Jeelani Basha Epimeric Excolides from the Stems of Excoecaria agallocha and Structural Revision of Rhizophorin A. Organic letters, 2015, 17, 2840-2843 |
1520000 | CIF | C29 H36 O8 | P 1 21/c 1 | 13.2416; 13.1779; 15.2428 90; 109.387; 90 | 2509 | Fukaya, Keisuke; Kodama, Keisuke; Tanaka, Yuta; Yamazaki, Hirohisa; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka Synthesis of Paclitaxel. 2. Construction of the ABCD Ring and Formal Synthesis. Organic letters, 2015, 17, 2574-2577 |
1520001 | CIF | C54 H46 Co N2 P3 | P 1 21/n 1 | 14.376; 14.699; 21.34 90; 107.79; 90 | 4293.8 | Scheuermann, Margaret L.; Johnson, Elizabeth J.; Chirik, Paul J. Alkene isomerization-hydroboration promoted by phosphine-ligated cobalt catalysts. Organic letters, 2015, 17, 2716-2719 |
1520002 | CIF | C29 H38 O8 | P 1 21/n 1 | 9.3612; 19.6336; 14.1965 90; 101.762; 90 | 2554.4 | Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization. Organic letters, 2015, 17, 2570-2573 |
1520003 | CIF Paper | C42 H50 O10 | P -1 | 9.6397; 13.6008; 15.0461 83.6966; 77.488; 77.9768 | 1879.2 | Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization. Organic letters, 2015, 17, 2570-2573 |
1520004 | CIF | C30.25 H41 O8 | P -1 | 11.3343; 15.4666; 16.487 85.1124; 78.3773; 78.5231 | 2771.3 | Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization. Organic letters, 2015, 17, 2570-2573 |
1520005 | CIF | C15 H21 N O2 | P 1 21/c 1 | 8.5353; 10.6984; 15.609 90; 104.429; 90 | 1380.4 | Zhou, Wei; Ni, Shengyang; Mei, Haibo; Han, Jianlin; Pan, Yi Hydroxyalkylation-initiated radical cyclization of N-allylbenzamide for direct construction of isoquinolinone. Organic letters, 2015, 17, 2724-2727 |
1520068 | CIF | C32 H36 Br2 N4 O2 | P 1 21/c 1 | 10.037; 8.2451; 18.991 90; 101.279; 90 | 1541.3 | Zhu, Xiaxia; Du, Haifeng A Highly Stereoselective Metal-Free Hydrogenation of Diimines for the Synthesis of Cis-Vicinal Diamines. Organic letters, 2015, 17, 3106-3109 |
1520116 | CIF | C28 H19 N | P -1 | 9.0455; 9.563; 11.529 103.716; 98.763; 98.986 | 938.1 | Liu, Xingyan; Li, Xiaoyu; Liu, Hu; Guo, Qiang; Lan, Jingbo; Wang, Ruilin; You, Jingsong Aldehyde as a Traceless Directing Group for Rh(III)-Catalyzed C-H Activation: A Facile Access to Diverse Indolo[1,2-a]quinolines. Organic letters, 2015, 17, 2936-2939 |
1520117 | CIF | C17.5 H18 F8 I O3.5 S2 | P -1 | 8.9435; 12.1892; 12.2642 63.163; 87.526; 77.6 | 1162.92 | Matsuzaki, Kohei; Okuyama, Kenta; Tokunaga, Etsuko; Saito, Norimichi; Shiro, Motoo; Shibata, Norio Synthesis of Diaryliodonium Salts Having Pentafluorosulfanylarenes and Their Application to Electrophilic Pentafluorosulfanylarylation of C-, O-, N-, and S-Nucleophiles. Organic letters, 2015, 17, 3038-3041 |
1520220 | CIF | C24 H19 N | C 1 2/c 1 | 42.784; 6.0454; 31.552 90; 119.951; 90 | 7071 | Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade. Organic letters, 2015, 17, 2984-2987 |
1520221 | CIF | C30 H23 N | P 1 21/c 1 | 12.0216; 6.2012; 30.083 90; 101.315; 90 | 2199 | Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade. Organic letters, 2015, 17, 2984-2987 |
1520222 | CIF | C23 H19 N | C 1 2/c 1 | 29.558; 6.041; 19.696 90; 104.661; 90 | 3402.4 | Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade. Organic letters, 2015, 17, 2984-2987 |
1520223 | CIF | C14 H16 Cl3 N O3 | P 32 | 16.1172; 16.1172; 5.6393 90; 90; 120 | 1268.63 | Skvorcova, Marija; Grigorjeva, Liene; Jirgensons, Aigars Tetrahydro-1,3-oxazepines via Intramolecular Amination of Cyclopropylmethyl Cation. Organic letters, 2015, 17, 2902-2904 |
1520224 | CIF | C22 H22 N4 O2 S | P 1 21 1 | 10.363; 9.318; 11.453 90; 112.7; 90 | 1020.3 | Wang, Linqing; Yang, Dongxu; Li, Dan; Wang, Rui Catalytic Enantioselective Ring-Opening and Ring-Closing Reactions of 3-Isothiocyanato Oxindoles and N-(2-Picolinoyl)aziridines. Organic letters, 2015, 17, 3004-3007 |
1520225 | CIF | C13 H21 N3 O3 | P 1 21/c 1 | 4.5905; 23.474; 13.2529 90; 91.746; 90 | 1427.4 | Martínez, Luís; Martorell, Gabriel; Sampedro, Ángel; Ballester, Pablo; Costa, Antoni; Rotger, Carmen Hydrogen Bonded Squaramide-Based Foldable Module Induces Both β- and α-Turns in Hairpin Structures of α-Peptides in Water. Organic letters, 2015, 17, 2980-2983 |
1520297 | CIF | C52 H60 Br N4 O18 S2 | C 1 2/c 1 | 26.6011; 19.037; 14.4208 90; 114.731; 90 | 6633 | Carrasco-Ruiz, Anayeli; Tiburcio, Jorge Electrostatic Kinetic Barriers in the Threading/Dethreading Motion of a Rotaxane-like Complex. Organic letters, 2015, 17, 1858-1861 |
1520298 | CIF | C52 H86 N4 O32 S2 | P 1 21/n 1 | 11.8381; 23.4128; 11.8991 90; 107.339; 90 | 3148.12 | Carrasco-Ruiz, Anayeli; Tiburcio, Jorge Electrostatic Kinetic Barriers in the Threading/Dethreading Motion of a Rotaxane-like Complex. Organic letters, 2015, 17, 1858-1861 |
1520299 | CIF | C22 H23 I O3 | P 21 21 21 | 5.7232; 10.8546; 32.913 90; 90; 90 | 2044.7 | Merad, Jérémy; Borkar, Prashant; Bouyon Yenda, Tracy; Roux, Christèle; Pons, Jean-Marc; Parrain, Jean-Luc; Chuzel, Olivier; Bressy, Cyril Highly Enantioselective Acylation of Acyclic Meso 1,3-Diols through Synergistic Isothiourea-Catalyzed Desymmetrization/Chiroablative Kinetic Resolution. Organic letters, 2015, 17, 2118-2121 |
1520300 | CIF | C36 H46 N4 O2 | P -1 | 7.1052; 14.1156; 16.3735 105.153; 91.858; 102.309 | 1541.85 | Meehan, Eileen; Li, Ruoshi; Zeller, Matthias; Brückner, Christian Octaethyl-1,3-oxazinochlorin: A β-Octaethylchlorin Analogue Made by Pyrrole Expansion. Organic letters, 2015, 17, 2210-2213 |
1520301 | CIF | C41 H58.333 N5 O | P 1 21/c 1 | 26.0651; 15.2582; 9.5468 90; 96.584; 90 | 3771.8 | Meehan, Eileen; Li, Ruoshi; Zeller, Matthias; Brückner, Christian Octaethyl-1,3-oxazinochlorin: A β-Octaethylchlorin Analogue Made by Pyrrole Expansion. Organic letters, 2015, 17, 2210-2213 |
1520302 | CIF | C33 H31 Br2 N O6 | P 1 21/c 1 | 18.4779; 9.1189; 19.3437 90; 109.352; 90 | 3075.2 | Tang, Shaojian; Park, Jong Yeun; Yeagley, Andrew A.; Sabat, Michal; Chruma, Jason J. Decarboxylative Generation of 2-Azaallyl Anions: 2-Iminoalcohols via a Decarboxylative Erlenmeyer Reaction. Organic letters, 2015, 17, 2042-2045 |
1520303 | CIF | C13 H23 Cl N2 Ni | P 1 21/n 1 | 11.1164; 12.6843; 11.5897 90; 118.363; 90 | 1438.02 | Shields, Jason D.; Gray, Erin E.; Doyle, Abigail G. A modular, air-stable nickel precatalyst. Organic letters, 2015, 17, 2166-2169 |
1520304 | CIF | C66.33 H81.67 N2 O4 Yb | P 21 21 21 | 15.592; 20.5827; 60.065 90; 90; 90 | 19276.4 | Zeng, Chao; Yuan, Dan; Zhao, Bei; Yao, Yingming Highly Enantioselective Epoxidation of α,β-Unsaturated Ketones Catalyzed by Rare-Earth Amides [(Me3Si)2N]3RE(μ-Cl)Li(THF)3 with Phenoxy-Functionalized Chiral Prolinols. Organic letters, 2015, 17, 2242-2245 |
1520305 | CIF | C6 H9 N O4 | C 1 2/c 1 | 16.4651; 6.6186; 14.9686 90; 109.033; 90 | 1542 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520306 | CIF | C12 H19 N O3 | P 1 21/c 1 | 11.0623; 9.4884; 11.6015 90; 90.961; 90 | 1217.56 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520307 | CIF | C10 H16 B F2 N O3 | P -1 | 9.5474; 11.4938; 11.5223 92.227; 96.964; 91.605 | 1253.45 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520308 | CIF | C12 H20 B F2 N O3 | P 1 21/n 1 | 7.8638; 14.0418; 12.6427 90; 91.6599; 90 | 1395.45 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
Back to the search form
Your own data is not in the COD? Deposit it, thanks!