Crystallography Open Database
Search results
Result: there are 136 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 Chemistry Frontiers' volume of publication is 2
COD ID ![]() |
Links | Formula ![]() |
Space group ![]() |
Cell parameters | Cell volume ![]() |
Bibliography |
---|---|---|---|---|---|---|
1553040 | CIF | C27 H31 N O6 S | P 1 21 1 | 18.2388; 14.6418; 20.7375 90; 90.251; 90 | 5537.9 | Liu, Feng; Wang, Yidong; Ye, Weiming; Zhang, Junliang Gold(i)-catalyzed asymmetric [3 + 2]-cycloadditions of γ-1-ethoxyethoxy-propiolates and aldehydes Organic Chemistry Frontiers, 2015, 2, 221 |
1553041 | CIF | C38 H42 Au Cl N O2 P | P 1 21 1 | 8.893; 20.6873; 9.7453 90; 105.318; 90 | 1729.17 | Liu, Feng; Wang, Yidong; Ye, Weiming; Zhang, Junliang Gold(i)-catalyzed asymmetric [3 + 2]-cycloadditions of γ-1-ethoxyethoxy-propiolates and aldehydes Organic Chemistry Frontiers, 2015, 2, 221 |
1553042 | CIF | C92 H98 N8 | P n n 2 | 15.865; 16.43; 14.961 90; 90; 90 | 3899.8 | Ie, Machiko; Setsune, Jun-ichiro; Eda, Kazuo; Tsuda, Akihiko Chiroptical sensing of oligonucleotides with a cyclic octapyrrole Organic Chemistry Frontiers, 2015, 2, 29 |
1553043 | CIF | C20 H20 N2 O2 | P 21 21 21 | 10.255; 10.8108; 15.4763 90; 90; 90 | 1715.8 | Yin, Xue-Song; Li, Yi-Chen; Yuan, Jun; Gu, Wen-Jia; Shi, Bing-Feng Copper(ii)-catalyzed methoxylation of unactivated (hetero)aryl C‒H bonds using a removable bidentate auxiliary Organic Chemistry Frontiers, 2015, 2, 119 |
1553044 | CIF | C17 H17 F3 N2 O2 | P 1 21/c 1 | 10.5428; 16.2625; 10.8624 90; 118.846; 90 | 1631.3 | Yin, Xue-Song; Li, Yi-Chen; Yuan, Jun; Gu, Wen-Jia; Shi, Bing-Feng Copper(ii)-catalyzed methoxylation of unactivated (hetero)aryl C‒H bonds using a removable bidentate auxiliary Organic Chemistry Frontiers, 2015, 2, 119 |
1553045 | CIF | C16 H19 N3 O2 | P -1 | 8.0742; 12.4409; 17.6473 71.94; 79.009; 72.177 | 1595.4 | Yin, Xue-Song; Li, Yi-Chen; Yuan, Jun; Gu, Wen-Jia; Shi, Bing-Feng Copper(ii)-catalyzed methoxylation of unactivated (hetero)aryl C‒H bonds using a removable bidentate auxiliary Organic Chemistry Frontiers, 2015, 2, 119 |
1553046 | CIF | C44 H33 F10 Ir N11 P | P -1 | 9.5524; 13.2533; 18.9296 101.946; 101.154; 103.248 | 2208 | Cai, Rong; Yan, Wuming; Bologna, Matthew G.; de Silva, Kaushalya; Ma, Zhao; Finklea, Harry O.; Petersen, Jeffrey L.; Li, Minyong; Shi, Xiaodong Synthesis and characterization of N-2-aryl-1,2,3-triazole based iridium complexes as photocatalysts with tunable photoredox potential Organic Chemistry Frontiers, 2015, 2, 141 |
1553047 | CIF | C34 H23 F2 Ir N8 O | P -1 | 11.0054; 14.2851; 21.789 71.698; 89.997; 67.306 | 2971.6 | Cai, Rong; Yan, Wuming; Bologna, Matthew G.; de Silva, Kaushalya; Ma, Zhao; Finklea, Harry O.; Petersen, Jeffrey L.; Li, Minyong; Shi, Xiaodong Synthesis and characterization of N-2-aryl-1,2,3-triazole based iridium complexes as photocatalysts with tunable photoredox potential Organic Chemistry Frontiers, 2015, 2, 141 |
1553048 | CIF | C27 H33 N O3 S Si | P 1 21/c 1 | 10.8466; 23.0405; 10.6995 90; 102.658; 90 | 2608.9 | Shen, Kun; Han, Xiuling; Xia, Guoqin; Lu, Xiyan Cationic Pd(ii)-catalyzed cyclization of N-tosyl-aniline tethered alkynyl ketones initiated by hydropalladation of alkynes: a facile way to 1,2-dihydro or 1,2,3,4-tetrahydroquinoline derivatives Organic Chemistry Frontiers, 2015, 2, 145 |
1553049 | CIF | C26 H28 Cl N O3 S Si | C 1 2/c 1 | 32.673; 12.2122; 12.9554 90; 92.633; 90 | 5163.9 | Shen, Kun; Han, Xiuling; Xia, Guoqin; Lu, Xiyan Cationic Pd(ii)-catalyzed cyclization of N-tosyl-aniline tethered alkynyl ketones initiated by hydropalladation of alkynes: a facile way to 1,2-dihydro or 1,2,3,4-tetrahydroquinoline derivatives Organic Chemistry Frontiers, 2015, 2, 145 |
1553050 | CIF | C32 H53 B11 N2 | P b c a | 17.5053; 20.281; 21.1684 90; 90; 90 | 7515.3 | Zheng, Fangrui; Xie, Zuowei Reaction of N-heterocyclic carbenes with 13-vertex closo-carboranes: synthesis and structural characterization of zwitterionic salts of 13-vertex nido-carboranes Organic Chemistry Frontiers, 2015, 2, 55 |
1553051 | CIF | C32 H55 B11 N2 | P b c a | 17.474; 20.161; 21.123 90; 90; 90 | 7441.5 | Zheng, Fangrui; Xie, Zuowei Reaction of N-heterocyclic carbenes with 13-vertex closo-carboranes: synthesis and structural characterization of zwitterionic salts of 13-vertex nido-carboranes Organic Chemistry Frontiers, 2015, 2, 55 |
1553052 | CIF | C26 H43 B11 N2 | P 21 21 21 | 11.591; 15.516; 16.796 90; 90; 90 | 3020.7 | Zheng, Fangrui; Xie, Zuowei Reaction of N-heterocyclic carbenes with 13-vertex closo-carboranes: synthesis and structural characterization of zwitterionic salts of 13-vertex nido-carboranes Organic Chemistry Frontiers, 2015, 2, 55 |
1553053 | CIF | C41 H63 B11 N2 O | P 21 21 21 | 10.343; 18.963; 22.347 90; 90; 90 | 4383 | Zheng, Fangrui; Xie, Zuowei Reaction of N-heterocyclic carbenes with 13-vertex closo-carboranes: synthesis and structural characterization of zwitterionic salts of 13-vertex nido-carboranes Organic Chemistry Frontiers, 2015, 2, 55 |
1553054 | CIF | C33 H55 B11 N2 | P b c a | 17.5189; 20.3686; 21.3348 90; 90; 90 | 7613 | Zheng, Fangrui; Xie, Zuowei Reaction of N-heterocyclic carbenes with 13-vertex closo-carboranes: synthesis and structural characterization of zwitterionic salts of 13-vertex nido-carboranes Organic Chemistry Frontiers, 2015, 2, 55 |
1553055 | CIF | C27 H43 B11 N2 | P 1 21/n 1 | 10.2998; 16.7445; 19.7479 90; 101.979; 90 | 3331.7 | Zheng, Fangrui; Xie, Zuowei Reaction of N-heterocyclic carbenes with 13-vertex closo-carboranes: synthesis and structural characterization of zwitterionic salts of 13-vertex nido-carboranes Organic Chemistry Frontiers, 2015, 2, 55 |
1553056 | CIF | C39 H59 B11 N2 | P 21 21 21 | 10.4375; 19.3175; 22.8874 90; 90; 90 | 4614.7 | Zheng, Fangrui; Xie, Zuowei Reaction of N-heterocyclic carbenes with 13-vertex closo-carboranes: synthesis and structural characterization of zwitterionic salts of 13-vertex nido-carboranes Organic Chemistry Frontiers, 2015, 2, 55 |
1553057 | CIF | C20 H23 N3 O2 S | P 1 21/n 1 | 9.2469; 12.1137; 17.1803 90; 99.893; 90 | 1895.8 | Zhu, Tong-Hao; Wei, Tian-Qi; Wang, Shun-Yi; Ji, Shun-Jun NIS/CHP-mediated reaction of isocyanides with hydrazones: access to aminopyrazoles Organic Chemistry Frontiers, 2015, 2, 259 |
1553058 | CIF | C25 H25 Br N2 O7 | P 21 21 21 | 10.943; 12.564; 18.454 90; 90; 90 | 2537.2 | Sun, Qiang-Sheng; Chen, Xiao-Yang; Zhu, Hua; Lin, Hua; Sun, Xing-Wen; Lin, Guo-Qiang Asymmetric synthesis of poly-substituted spirocyclohexane oxindole via a squaramide catalyzed cascade Michael‒Michael‒aldol sequence Organic Chemistry Frontiers, 2015, 2, 110 |
1553059 | CIF | C17 H18 Br N O5 | P 21 21 21 | 6.6023; 7.8736; 32.754 90; 90; 90 | 1702.7 | Li, Ying-Zi; Wang, Jie; Sun, Wang-Bin; Shan, Yi-Fan; Sun, Bing-Feng; Lin, Guo-Qiang; Zou, Jian-Ping Enantioselective synthesis of bicyclo[2.2.2]octane-1-carboxylates under metal free conditions Organic Chemistry Frontiers, 2015, 2, 274 |
1553060 | CIF | C12 H17 N O4 S | P 21 21 21 | 8.7741; 9.7409; 14.5365 90; 90; 90 | 1242.4 | Riaño, Iker; Uria, Uxue; Carrillo, Luisa; Reyes, Efraim; Vicario, Jose L. 4-Alkenyl-5H-1,2,3-oxathiazole 2,2-dioxides in catalytic and enantioselective [4 + 2] cycloaddition through iminium activation. Straightforward access to the trans-decaline framework and to densely functionalized cyclohexanes Organic Chemistry Frontiers, 2015, 2, 206 |
1553061 | CIF | C8 H10 O3 | P -1 | 3.9045; 9.1939; 22.5383 88.422; 88.131; 78.161 | 791.26 | Wang, Qiang; Xu, Qin; Shi, Min Co-catalysis between DABCO and a Brønsted acid in the catalytic [4 + 2] annulation of isatin with but-3-yn-2-one and mechanistic investigations Organic Chemistry Frontiers, 2015, 2, 211 |
1553062 | CIF | C21 H19 N O3 | P -1 | 8.1086; 8.8324; 13.26 108.838; 97.636; 94.663 | 883 | Wang, Qiang; Xu, Qin; Shi, Min Co-catalysis between DABCO and a Brønsted acid in the catalytic [4 + 2] annulation of isatin with but-3-yn-2-one and mechanistic investigations Organic Chemistry Frontiers, 2015, 2, 211 |
1553063 | CIF | C77 H89 Br4 Cl3 F8 I4 N4 O8 | P 4/n c c :2 | 18.4165; 18.4165; 27.9044 90; 90; 90 | 9464.3 | Beyeh, N. Kodiah; Valkonen, Arto; Bhowmik, Sandip; Pan, Fangfang; Rissanen, K. N-Alkyl ammonium resorcinarene salts: multivalent halogen-bonded deep-cavity cavitands Organic Chemistry Frontiers, 2015, 2, 340 |
1553064 | CIF | C72 H114 Br4 Cl2 N4 O9 | P b c a | 23.3371; 23.5232; 27.0473 90; 90; 90 | 14848 | Beyeh, N. Kodiah; Valkonen, Arto; Bhowmik, Sandip; Pan, Fangfang; Rissanen, K. N-Alkyl ammonium resorcinarene salts: multivalent halogen-bonded deep-cavity cavitands Organic Chemistry Frontiers, 2015, 2, 340 |
1553065 | CIF | C7 H7 Cl N O2 | C 1 2/c 1 | 24.849; 4.7231; 14.8643 90; 103.467; 90 | 1696.6 | Barnes, Korry L.; Chen, Kelly; Catalano, Vincent J.; Jeffrey, Christopher S. New building blocks for iminosugars: a concise synthesis of polyhydroxylated N-alkoxypiperidines through an intramolecular azepine ring contraction Organic Chemistry Frontiers, 2015, 2, 497 |
1553066 | CIF | C13 H17 N O3 | P -1 | 9.9549; 11.3328; 11.8818 106.461; 101.618; 100.174 | 1219.6 | Barnes, Korry L.; Chen, Kelly; Catalano, Vincent J.; Jeffrey, Christopher S. New building blocks for iminosugars: a concise synthesis of polyhydroxylated N-alkoxypiperidines through an intramolecular azepine ring contraction Organic Chemistry Frontiers, 2015, 2, 497 |
1553067 | CIF | C13 H19 N O5 | P -1 | 5.3906; 15.9299; 17.3564 112.457; 97.7331; 99.3952 | 1326.85 | Barnes, Korry L.; Chen, Kelly; Catalano, Vincent J.; Jeffrey, Christopher S. New building blocks for iminosugars: a concise synthesis of polyhydroxylated N-alkoxypiperidines through an intramolecular azepine ring contraction Organic Chemistry Frontiers, 2015, 2, 497 |
1553068 | CIF | C15 H11 N O2 | P -1 | 7.1432; 8.4932; 10.1874 99.388; 97.577; 106.771 | 573.27 | Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds Organic Chemistry Frontiers, 2015, 2, 312 |
1553069 | CIF | C22 H20 N2 O4 | P 1 21/n 1 | 7.0179; 4.6365; 29.074 90; 92.757; 90 | 944.93 | Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds Organic Chemistry Frontiers, 2015, 2, 312 |
1553070 | CIF | C21 H21 N3 O | P 1 c 1 | 18.2723; 5.5654; 8.7266 90; 103.633; 90 | 862.43 | Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds Organic Chemistry Frontiers, 2015, 2, 312 |
1553071 | CIF | C23 H16 O | P 1 21 1 | 11.008; 7.5883; 19.571 90; 90.988; 90 | 1634.6 | Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds Organic Chemistry Frontiers, 2015, 2, 312 |
1553072 | CIF | C22 H23 N O2 | P -1 | 9.1264; 9.7169; 10.2731 95.504; 91.157; 101.221 | 888.78 | Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds Organic Chemistry Frontiers, 2015, 2, 312 |
1553073 | CIF | C20 H18 N4 O2 | P -1 | 5.6257; 19.7469; 23.768 79.737; 88.28; 82.746 | 2577.3 | Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds Organic Chemistry Frontiers, 2015, 2, 312 |
1553074 | CIF | C20 H13 N O4 | P -1 | 7.1728; 8.0196; 12.8455 84.142; 89.687; 87.901 | 734.56 | Chahdoura, Faouzi; Mallet-Ladeira, Sonia; Gómez, Montserrat Palladium nanoparticles in glycerol: a clear-cut catalyst for one-pot multi-step processes applied in the synthesis of heterocyclic compounds Organic Chemistry Frontiers, 2015, 2, 312 |
1553075 | CIF | C9 H9 N7 O | P c a 21 | 9.9162; 14.8123; 7.3118 90; 90; 90 | 1073.97 | Quinodoz, Pierre; Lo, Cheikh; Kletskii, Mikhail; Burov, Oleg; Marrot, Jérôme; Couty, François Regio- and stereoselective synthesis of α-hydroxy-β-azido tetrazoles Organic Chemistry Frontiers, 2015, 2, 492 |
1553076 | CIF | C15 H13 N O5 S | P 32 | 10.3879; 10.3879; 24.218 90; 90; 120 | 2263.2 | Quan, Mao; Yang, Guoqiang; Xie, Fang; Gridnev, Ilya D.; Zhang, Wanbin Pd(ii)-catalyzed asymmetric addition of arylboronic acids to cyclic N-sulfonyl ketimine esters and a DFT study of its mechanism Organic Chemistry Frontiers, 2015, 2, 398 |
1553095 | CIF | C14 H16 O3 | P -1 | 9.017; 12.174; 12.8341 108.889; 99.634; 109.852 | 1191.34 | Dethe, Dattatraya H.; Boda, Raghavender; Murhade, Ganesh M. Lewis acid catalyzed Nazarov type cyclization for the synthesis of a substituted indane framework: total synthesis of (±)-mutisianthol Organic Chemistry Frontiers, 2015, 2, 645 |
1553096 | CIF | C56 H79 B5 O10 | P 21 21 21 | 12.38928; 20.5595; 23.639 90; 90; 90 | 6021.26 | Da Ros, Sara; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S. Boronic esters of corannulene: potential building blocks toward icosahedral supramolecules Organic Chemistry Frontiers, 2015, 2, 626 |
1553097 | CIF | C46 H46 B5 Cl3 O10 | P m n 21 | 20.2644; 13.18215; 8.2499 90; 90; 90 | 2203.78 | Da Ros, Sara; Linden, Anthony; Baldridge, Kim K.; Siegel, Jay S. Boronic esters of corannulene: potential building blocks toward icosahedral supramolecules Organic Chemistry Frontiers, 2015, 2, 626 |
1553098 | CIF | C32 H22 Cl2 Si | P 1 21/c 1 | 9.959; 24.396; 11.0384 90; 108.602; 90 | 2541.8 | Xu, Liang; Zhang, Shuai; Li, Pengfei Synthesis of silafluorenes and silaindenes via silyl radicals from arylhydrosilanes: intramolecular cyclization and intermolecular annulation with alkynes Organic Chemistry Frontiers, 2015, 2, 459 |
1553099 | CIF | C25 H29 N O3 | P 21 21 21 | 5.572; 15.48; 25.4858 90; 90; 90 | 2198.3 | Arena, Giada; Cini, Elena; Petricci, Elena; Randino, Rosario; Taddei, Maurizio A highly stereo-controlled protocol to prepare pipecolic acids based on Heck and cyclohydrocarbonylation reactions Organic Chemistry Frontiers, 2015, 2, 526 |
1553100 | CIF | C23 H16 O3.19 | P 1 21/c 1 | 22.264; 10.1945; 30.92 90; 91.849; 90 | 7014 | Liu, Tong; Ding, Qiuping; Zong, Qianshou; Qiu, Guanyinsheng Radical 5-exo cyclization of alkynoates with 2-oxoacetic acids for synthesis of 3-acylcoumarins Organic Chemistry Frontiers, 2015, 2, 670 |
1553101 | CIF | C18 H13 N O2 | P -1 | 7.159; 9.364; 10.541 78.846; 82.356; 72.557 | 659.3 | Dethe, Dattatraya H.; Kumar B, Vijay Concise asymmetric total synthesis of bruceolline J Organic Chemistry Frontiers, 2015, 2, 548 |
1553102 | CIF | C30 H24 F12 N6 Ru Sb2 | P -3 c 1 | 10.786; 10.786; 17.286 90; 90; 120 | 1741.59 | Gomes, Filipe; Narbonne, Vanessa; Blanchard, Florent; Maestri, Giovanni; Malacria, Max Formal base-free homolytic aromatic substitutions via photoredox catalysis Organic Chemistry Frontiers, 2015, 2, 464 |
1553103 | CIF | C16 H22 N O3 S | P -1 | 6.2097; 11.272; 11.547 104.782; 101.238; 100.235 | 744.1 | Zhang, Yan-Yan; Hao, Jian; Shi, Min One pot cascade synthesis of fused heterocycles from furan-tethered terminal alkynes and aldehydes in the presence of amines and CuBr Organic Chemistry Frontiers, 2015, 2, 394 |
1553104 | CIF | C16 H17 N O3 S | P -1 | 8.3878; 9.8582; 19.139 76.354; 84.421; 73.985 | 1477.3 | Zhang, Yan-Yan; Hao, Jian; Shi, Min One pot cascade synthesis of fused heterocycles from furan-tethered terminal alkynes and aldehydes in the presence of amines and CuBr Organic Chemistry Frontiers, 2015, 2, 394 |
1553105 | CIF | C17 H19 N O3 S | P 1 21/c 1 | 14.5933; 9.6858; 11.3977 90; 92.745; 90 | 1609.2 | Zhang, Yan-Yan; Hao, Jian; Shi, Min One pot cascade synthesis of fused heterocycles from furan-tethered terminal alkynes and aldehydes in the presence of amines and CuBr Organic Chemistry Frontiers, 2015, 2, 394 |
1553106 | CIF | C33 H30 Br N O5 | I 2 2 2 | 15.713; 28.08; 28.507 90; 90; 90 | 12578 | Zhang, Jun-Wei; Liu, Xiao-Wei; Gu, Qing; Shi, Xiao-Xin; You, Shu-Li Enantioselective synthesis of 4,5,6,7-tetrahydroindoles via olefin cross-metathesis/intramolecular Friedel‒Crafts alkylation reaction of pyrroles Organic Chemistry Frontiers, 2015, 2, 476 |
1553107 | CIF | C17 H0 I2 N3 O6 | P 1 21/c 1 | 5.5881; 18.985; 10.6706 90; 94.113; 90 | 1129.13 | Zhang, Shuo; Chen, Ying; Wang, Jianwu; Pan, Yue; Xu, Zhenghu; Tung, Chen-Ho An efficient synthesis of gem-diiodoolefins and (E)-iodoalkenes from propargylic amides with a Cu(i)/Cu(iii) cycle Organic Chemistry Frontiers, 2015, 2, 578 |
1553108 | CIF | C23 H25 N O5 | P -1 | 9.2215; 10.9612; 11.6484 87.764; 69.092; 73.409 | 1051.48 | Zhang, Shuo; Chen, Ying; Wang, Jianwu; Pan, Yue; Xu, Zhenghu; Tung, Chen-Ho An efficient synthesis of gem-diiodoolefins and (E)-iodoalkenes from propargylic amides with a Cu(i)/Cu(iii) cycle Organic Chemistry Frontiers, 2015, 2, 578 |
1553109 | CIF | C23 H17 I O3 | C 1 2/c 1 | 26.291; 8.781; 18.363 90; 111.863; 90 | 3934 | Zhu, Hai-Tao; Fan, Ming-Jin; Yang, De-Suo; Wang, Xiao-Ling; Ke, Sen; Zhang, Chao-Yang; Guan, Zheng-Hui An iodine-promoted Meyer‒Schuster rearrangement for the synthesis of α-iodo unsaturated ketones Organic Chemistry Frontiers, 2015, 2, 506 |
1553110 | CIF | C59 H49 Cl4 F6 N P3 Rh | P 1 21/c 1 | 12.3535; 28.8354; 15.2713 90; 99.472; 90 | 5365.7 | Chen, Shanshan; Su, Yan; Han, Keli; Li, Xingwei Mechanistic studies on C‒C reductive coupling of five-coordinate Rh(iii) complexes Organic Chemistry Frontiers, 2015, 2, 783 |
1553111 | CIF | C65 H61 F6 N O2 P3 Rh | P -1 | 10.8319; 13.2288; 22.0889 75.156; 79.856; 69.201 | 2847.44 | Chen, Shanshan; Su, Yan; Han, Keli; Li, Xingwei Mechanistic studies on C‒C reductive coupling of five-coordinate Rh(iii) complexes Organic Chemistry Frontiers, 2015, 2, 783 |
1553112 | CIF | C59 H46 Cl2 F9 N P3 Rh | P 1 21/n 1 | 13.6534; 25.7008; 15.5862 90; 93.092; 90 | 5461.29 | Chen, Shanshan; Su, Yan; Han, Keli; Li, Xingwei Mechanistic studies on C‒C reductive coupling of five-coordinate Rh(iii) complexes Organic Chemistry Frontiers, 2015, 2, 783 |
1553113 | CIF | C58 H52 B Cl6 F4 N O Os P2 | P 1 21/n 1 | 16.5731; 19.6848; 18.1839 90; 112.182; 90 | 5493.2 | Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping Reactions of osmapyridinium with terminal alkynes Organic Chemistry Frontiers, 2015, 2, 560 |
1553114 | CIF | C56.25 H52.25 B Cl2.75 F4 N O3 Os P2 | P 1 21/c 1 | 11.9299; 14.1946; 33.0235 90; 98.576; 90 | 5529.7 | Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping Reactions of osmapyridinium with terminal alkynes Organic Chemistry Frontiers, 2015, 2, 560 |
1553115 | CIF | C50 H43 B Cl5 F4 N3 O Os P | P 1 21/c 1 | 12.0746; 18.8448; 20.9677 90; 90.023; 90 | 4771.06 | Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping Reactions of osmapyridinium with terminal alkynes Organic Chemistry Frontiers, 2015, 2, 560 |
1553116 | CIF | C52 H55 B Cl4 F4 N3 Os P | C 1 c 1 | 19.3445; 16.8974; 16.1902 90; 111.004; 90 | 4940.5 | Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping Reactions of osmapyridinium with terminal alkynes Organic Chemistry Frontiers, 2015, 2, 560 |
1553117 | CIF | C19 H21 N O3 | P 1 21/c 1 | 7.2941; 13.2249; 17.2264 90; 96.919; 90 | 1649.62 | Santos, Hugo; Distiller, Amy; D'Souza, Asha M.; Arnoux, Quentin; White, Jonathan M.; Meyer, Adam G.; Ryan, John H. 1,3-Dipolar cycloaddition reactions of phthalic anhydrides with an azomethine ylide Organic Chemistry Frontiers, 2015, 2, 705 |
1553118 | CIF | C32 H37 N O4 S Sn | P 1 21 1 | 8.592; 10.956; 16.545 90; 92.673; 90 | 1556 | Kamimura, Akio; Yoshinaga, Tatsuro; Noguchi, Fumiaki; Miyazaki, Koichiro; Uno, Hidemitsu A mechanistic study on the SHi reaction at tin atoms in a radical cascade reaction Organic Chemistry Frontiers, 2015, 2, 713 |
1553119 | CIF | C16 H16 Cl I O S | P 21 21 21 | 7.6495; 12.803; 16.9343 90; 90; 90 | 1658.5 | Berthelot-Bréhier, Anaïs; Panossian, Armen; Colobert, Françoise; Leroux, Frédéric R. Atroposelective synthesis of axially chiral P,S-ligands based on arynes Organic Chemistry Frontiers, 2015, 2, 634 |
1553120 | CIF | C28 H26 Cl P S | P 21 21 21 | 9.4309; 13.5255; 19.3191 90; 90; 90 | 2464.3 | Berthelot-Bréhier, Anaïs; Panossian, Armen; Colobert, Françoise; Leroux, Frédéric R. Atroposelective synthesis of axially chiral P,S-ligands based on arynes Organic Chemistry Frontiers, 2015, 2, 634 |
1553121 | CIF | C35 H34 Cl3 P Pd S | P 21 21 21 | 11.8312; 15.3726; 17.795 90; 90; 90 | 3236.49 | Berthelot-Bréhier, Anaïs; Panossian, Armen; Colobert, Françoise; Leroux, Frédéric R. Atroposelective synthesis of axially chiral P,S-ligands based on arynes Organic Chemistry Frontiers, 2015, 2, 634 |
1553122 | CIF | C19 H20 F3 N | P 1 21 1 | 10.4422; 33.2582; 10.4466 90; 114.77; 90 | 3294.2 | Chen, Mu-Wang; Ye, Zhi-Shi; Chen, Zhang-Pei; Wu, Bo; Zhou, Yong-Gui Enantioselective synthesis of trifluoromethyl substituted piperidines with multiple stereogenic centers via hydrogenation of pyridinium hydrochlorides Organic Chemistry Frontiers, 2015, 2, 586 |
1553123 | CIF | C23 H35 N S Si Ti | P 1 21/c 1 | 18.029; 9.695; 14.246 90; 110.517; 90 | 2332.1 | Suzuki, Noriyuki; Asada, Takumi; Kawamura, Akiko; Masuyama, Yoshiro Sulfur-containing stable five-membered “cycloallene” complexes: 1-thia-2-zircona- and 1-thia-2-titanacyclopenta-3,4-dienes Organic Chemistry Frontiers, 2015, 2, 681 |
1553124 | CIF | C23 H35 N S Si Zr | P 1 21/c 1 | 18.125; 9.87; 14.346 90; 110.563; 90 | 2402.9 | Suzuki, Noriyuki; Asada, Takumi; Kawamura, Akiko; Masuyama, Yoshiro Sulfur-containing stable five-membered “cycloallene” complexes: 1-thia-2-zircona- and 1-thia-2-titanacyclopenta-3,4-dienes Organic Chemistry Frontiers, 2015, 2, 681 |
1553125 | CIF | C18 H25 N S Si Zr | P 1 21/c 1 | 15.471; 9.164; 14.06 90; 108.282; 90 | 1892.8 | Suzuki, Noriyuki; Asada, Takumi; Kawamura, Akiko; Masuyama, Yoshiro Sulfur-containing stable five-membered “cycloallene” complexes: 1-thia-2-zircona- and 1-thia-2-titanacyclopenta-3,4-dienes Organic Chemistry Frontiers, 2015, 2, 681 |
1553126 | CIF | C8 H17 N S Si | P -1 | 6.2605; 6.9304; 14.4299 92.0278; 99.0665; 112.207 | 569.305 | Suzuki, Noriyuki; Asada, Takumi; Kawamura, Akiko; Masuyama, Yoshiro Sulfur-containing stable five-membered “cycloallene” complexes: 1-thia-2-zircona- and 1-thia-2-titanacyclopenta-3,4-dienes Organic Chemistry Frontiers, 2015, 2, 681 |
1553127 | CIF | C18 H16 O2 S | P 1 21/n 1 | 8.3022; 11.1608; 16.3992 90; 94.272; 90 | 1515.31 | Chen, Dianpeng; Xing, Gangdong; Zhou, Hongwei Sulfone promoted Rh(iii)-catalyzed C‒H activation and base assisted 1,5-H shift strategy for the construction of seven-membered rings Organic Chemistry Frontiers, 2015, 2, 947 |
1553128 | CIF | C17 H21 N O3 | P -1 | 8.6808; 8.9707; 11.2873 104.818; 112.003; 92.742 | 777.67 | Liu, Xianglei; Gu, Zhenhua Pd-catalyzed Heck cyclization and in situ hydrocarboxylation or hydromethenylation via a hydrogen borrowing strategy Organic Chemistry Frontiers, 2015, 2, 778 |
1553129 | CIF | C16 H25 F O2 | P 21 21 21 | 5.9958; 13.644; 17.789 90; 90; 90 | 1455.3 | Zhang, Xiaofei; Guo, Shuo; Tang, Pingping Transition-metal free oxidative aliphatic C‒H fluorination Organic Chemistry Frontiers, 2015, 2, 806 |
1553130 | CIF | C24 H31 F O8 | P 21 21 21 | 8.7359; 12.804; 20.625 90; 90; 90 | 2307 | Zhang, Xiaofei; Guo, Shuo; Tang, Pingping Transition-metal free oxidative aliphatic C‒H fluorination Organic Chemistry Frontiers, 2015, 2, 806 |
1553131 | CIF | C16 H24 Cl2 N2 O Pd | P 1 21 1 | 12.1876; 9.8204; 15.854 90; 96.796; 90 | 1884.2 | Yu, Feng; Chen, Pinhong; Liu, Guosheng Pd(ii)-catalyzed intermolecular enantioselective hydroamination of styrenes Organic Chemistry Frontiers, 2015, 2, 819 |
1553132 | CIF | C2.889 H5.111 N0.222 O0.667 S0.222 | P 1 21 1 | 10.291; 5.9808; 12.068 90; 103.531; 90 | 722.1 | Ye, Jian-Liang; Zhang, Yu-Feng; Liu, Yang; Zhang, Jin-Yuan; Ruan, Yuan-Ping; Huang, Pei-Qiang Studies on the asymmetric synthesis of pandamarilactonines: an unexpected syn-selective vinylogous Mannich reaction of N-tert-butanesulfinimines Organic Chemistry Frontiers, 2015, 2, 697 |
1553133 | CIF | C33 H36 N O8 P S | P -1 | 10.3564; 12.0563; 14.1956 69.77; 82.139; 68.496 | 1547.3 | Kondoh, Azusa; Terada, Masahiro Brønsted base-catalyzed α-oxygenation of carbonyl compounds utilizing the [1,2]-phospha-Brook rearrangement Organic Chemistry Frontiers, 2015, 2, 801 |
1553134 | CIF | C11 H13 N O7 S2 | P 21 21 21 | 7.82043; 10.2265; 17.491 90; 90; 90 | 1398.85 | Kang, Jian; Zhu, Baofu; Liu, Jiewei; Wang, Bo; Zhang, Li; Su, Cheng-Yong Chiral dirhodium catalysts derived from l-serine, l-threonine and l-cysteine: design, synthesis and application Organic Chemistry Frontiers, 2015, 2, 890 |
1553135 | CIF | C11 H12 N2 O7 S | P 41 | 15.41418; 15.41418; 5.95145 90; 90; 90 | 1414.05 | Kang, Jian; Zhu, Baofu; Liu, Jiewei; Wang, Bo; Zhang, Li; Su, Cheng-Yong Chiral dirhodium catalysts derived from l-serine, l-threonine and l-cysteine: design, synthesis and application Organic Chemistry Frontiers, 2015, 2, 890 |
1553136 | CIF | C14 H14 N2 O3 | P 1 2/c 1 | 12.8276; 8.4882; 24.8068 90; 91.044; 90 | 2700.6 | Zhang, Duo; Cui, Xiuling; Yang, Fangfang; Zhang, Qianqian; Zhu, Yu; Wu, Yangjie Palladium-catalyzed direct ortho C‒O bond construction of azoxybenzenes with carboxylic acids and alcohols Organic Chemistry Frontiers, 2015, 2, 951 |
1553137 | CIF | C28 H21 F3 N4 O6 Pd2 | P 1 21/c 1 | 14.4863; 17.2032; 11.5651 90; 105.969; 90 | 2770.93 | Zhang, Duo; Cui, Xiuling; Yang, Fangfang; Zhang, Qianqian; Zhu, Yu; Wu, Yangjie Palladium-catalyzed direct ortho C‒O bond construction of azoxybenzenes with carboxylic acids and alcohols Organic Chemistry Frontiers, 2015, 2, 951 |
1553138 | CIF | C17 H18 N2 O3 | P -1 | 6.8879; 8.282; 14.4023 104.655; 94.121; 91.668 | 791.85 | Zhang, Duo; Cui, Xiuling; Yang, Fangfang; Zhang, Qianqian; Zhu, Yu; Wu, Yangjie Palladium-catalyzed direct ortho C‒O bond construction of azoxybenzenes with carboxylic acids and alcohols Organic Chemistry Frontiers, 2015, 2, 951 |
1553139 | CIF | C20 H26 N O2 S | P -1 | 8.6248; 9.8158; 11.6537 99.05; 101.411; 96.596 | 944.1 | Pan, Dong; Chen, Gen-Qiang; Tang, Xiang-Ying; Shi, Min Palladium-catalyzed intramolecular rearrangement of vinylidenecyclopropanes through C‒C bond activation Organic Chemistry Frontiers, 2015, 2, 792 |
1553140 | CIF | C30 H31 N O2 S | P 1 21/n 1 | 8.5768; 10.2978; 28.986 90; 90.183; 90 | 2560.1 | Pan, Dong; Chen, Gen-Qiang; Tang, Xiang-Ying; Shi, Min Palladium-catalyzed intramolecular rearrangement of vinylidenecyclopropanes through C‒C bond activation Organic Chemistry Frontiers, 2015, 2, 792 |
1553141 | CIF | C21 H22 Br N3 O5 | P 1 21 1 | 9.8915; 9.4814; 11.942 90; 102.048; 90 | 1095.31 | Hu, Ying; Zhou, Zijun; Gong, Lei; Meggers, Eric Asymmetric aza-Henry reaction to provide oxindoles with quaternary carbon stereocenter catalyzed by a metal-templated chiral Brønsted base Organic Chemistry Frontiers, 2015, 2, 968 |
1553142 | CIF | C14 H15 Br N2 O3 | P n a 21 | 7.1573; 21.4898; 9.4975 90; 90; 90 | 1460.8 | Hu, Ying; Zhou, Zijun; Gong, Lei; Meggers, Eric Asymmetric aza-Henry reaction to provide oxindoles with quaternary carbon stereocenter catalyzed by a metal-templated chiral Brønsted base Organic Chemistry Frontiers, 2015, 2, 968 |
1553143 | CIF | C70 H66 Cl34 N8 P2 Ru2 | P 1 21/n 1 | 13.25; 16.9695; 23.3436 90; 103.948; 90 | 5093.95 | Mejuto, Carmen; García-Eleno, Marco A.; Guisado-Barrios, Gregorio; Spasyuk, Denis; Gusev, Dmitri; Peris, Eduardo Ruthenium complexes with an N-heterocyclic carbene NNC-pincer ligand: preparation and catalytic properties Organic Chemistry Frontiers, 2015, 2, 936 |
1553144 | CIF | C32 H35 Cl2 N4 O5 P Ru | P 1 21/c 1 | 18.2792; 11.74106; 17.1049 90; 117.389; 90 | 3259.49 | Mejuto, Carmen; García-Eleno, Marco A.; Guisado-Barrios, Gregorio; Spasyuk, Denis; Gusev, Dmitri; Peris, Eduardo Ruthenium complexes with an N-heterocyclic carbene NNC-pincer ligand: preparation and catalytic properties Organic Chemistry Frontiers, 2015, 2, 936 |
1553145 | CIF | C26 H17 O3 P | P 21 21 21 | 8.4926; 12.013; 19.248 90; 90; 90 | 1963.7 | Xu, Guangqing; Li, Minghong; Wang, Shouliang; Tang, Wenjun Efficient synthesis of P-chiral biaryl phosphonates by stereoselective intramolecular cyclization Organic Chemistry Frontiers, 2015, 2, 1342 |
1553146 | CIF | C25 H23 Au I N3 O | C 1 2/c 1 | 32.577; 10.964; 15.077 90; 101.267; 90 | 5281.3 | Xu, Qin; Gu, Peng; Wang, Feijun; Shi, Min Selectfluor promoted NHC‒oxazoline gold(i) complex catalyzed cycloaddition/oxidation reaction of enynones with alkenes Organic Chemistry Frontiers, 2015, 2, 1475 |
1553147 | CIF | C23 H19 Au I N3 O | P 21 21 21 | 10.3025; 16.0231; 26.3966 90; 90; 90 | 4357.5 | Xu, Qin; Gu, Peng; Wang, Feijun; Shi, Min Selectfluor promoted NHC‒oxazoline gold(i) complex catalyzed cycloaddition/oxidation reaction of enynones with alkenes Organic Chemistry Frontiers, 2015, 2, 1475 |
1553148 | CIF | C24 H34 O10 | P 21 21 21 | 5.8507; 14.177; 30.834 90; 90; 90 | 2557.5 | Huang, Xin; Xue, Can; Fu, Chunling; Ma, Shengming A concise construction of carbohydrate-tethered axially chiral allenes via copper catalysis Organic Chemistry Frontiers, 2015, 2, 1040 |
1553149 | CIF | C21 H19 N O6 | P 21 21 21 | 10.8569; 14.913; 23.1808 90; 90; 90 | 3753.2 | Duan, Jindian; Cheng, Jing; Li, Pengfei Enantioselective construction of spiro-1,3-indandiones with three stereocenters via organocatalytic Michael-aldol reaction of 2-arylideneindane-1,3-diones and nitro aldehydes Organic Chemistry Frontiers, 2015, 2, 1048 |
1553150 | CIF | C72 H74 I2 N36 O16 | P n a 21 | 13.093; 25.621; 27.14 90; 90; 90 | 9104 | Zhou, Tian-You; Qi, Qiao-Yan; Zhang, Ying; Xu, Xiao-Na; Zhao, Xin A thermally stable pH-responsive “supramolecular buckle” based on the encapsulation of 4-(4-aminophenyl)-N-methylpyridinium by cucurbit[8]uril Organic Chemistry Frontiers, 2015, 2, 1030 |
1553151 | CIF | C18 H19 N O2 | C 1 2/c 1 | 20.293; 6.84225; 22.5979 90; 90.8593; 90 | 3137.36 | Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S. γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines Organic Chemistry Frontiers, 2015, 2, 1445 |
1553152 | CIF | C18 H19 N O2 | P 1 21/c 1 | 7.63367; 29.2305; 6.84862 90; 102.295; 90 | 1493.12 | Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S. γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines Organic Chemistry Frontiers, 2015, 2, 1445 |
1553153 | CIF | C19 H21 N O2 | P b c a | 12.4972; 14.1613; 17.5538 90; 90; 90 | 3106.61 | Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S. γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines Organic Chemistry Frontiers, 2015, 2, 1445 |
1553154 | CIF | C16 H17 N O3 | P 21 21 21 | 6.86998; 15.21957; 27.0563 90; 90; 90 | 2828.96 | Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S. γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines Organic Chemistry Frontiers, 2015, 2, 1445 |
1553155 | CIF | C19 H21 N O3 | P -1 | 6.98428; 15.3845; 16.6168 110.497; 97.0023; 102.274 | 1596.16 | Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S. γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines Organic Chemistry Frontiers, 2015, 2, 1445 |
1553156 | CIF | C18 H20 N2 O3 | P -1 | 6.8071; 15.0202; 15.8559 90.798; 101.156; 100.035 | 1564.3 | Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S. γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines Organic Chemistry Frontiers, 2015, 2, 1445 |
1553157 | CIF | C11 H14 N2 O2 | P -1 | 7.5414; 11.8446; 12.2635 80.154; 88.093; 88.519 | 1078.48 | Hama Salih, Mariwan A.; Male, Louise; Spencer, Neil; Fossey, John S. γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines Organic Chemistry Frontiers, 2015, 2, 1445 |
Back to the search form
Your own data is not in the COD? Deposit it, thanks!