Crystallography Open Database

Result: there are 136 entries in the selection

Switch to the old layout of the page

Download 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

Left arrow Left arrow First | Left arrow Previous 100 | of 2 | Next 100 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
1553040 CIFC27 H31 N O6 SP 1 21 118.2388; 14.6418; 20.7375
90; 90.251; 90
5537.9Liu, 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 CIFC38 H42 Au Cl N O2 PP 1 21 18.893; 20.6873; 9.7453
90; 105.318; 90
1729.17Liu, 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 CIFC92 H98 N8P n n 215.865; 16.43; 14.961
90; 90; 90
3899.8Ie, Machiko; Setsune, Jun-ichiro; Eda, Kazuo; Tsuda, Akihiko
Chiroptical sensing of oligonucleotides with a cyclic octapyrrole
Organic Chemistry Frontiers, 2015, 2, 29
1553043 CIFC20 H20 N2 O2P 21 21 2110.255; 10.8108; 15.4763
90; 90; 90
1715.8Yin, 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 CIFC17 H17 F3 N2 O2P 1 21/c 110.5428; 16.2625; 10.8624
90; 118.846; 90
1631.3Yin, 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 CIFC16 H19 N3 O2P -18.0742; 12.4409; 17.6473
71.94; 79.009; 72.177
1595.4Yin, 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 CIFC44 H33 F10 Ir N11 PP -19.5524; 13.2533; 18.9296
101.946; 101.154; 103.248
2208Cai, 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 CIFC34 H23 F2 Ir N8 OP -111.0054; 14.2851; 21.789
71.698; 89.997; 67.306
2971.6Cai, 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 CIFC27 H33 N O3 S SiP 1 21/c 110.8466; 23.0405; 10.6995
90; 102.658; 90
2608.9Shen, 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 CIFC26 H28 Cl N O3 S SiC 1 2/c 132.673; 12.2122; 12.9554
90; 92.633; 90
5163.9Shen, 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 CIFC32 H53 B11 N2P b c a17.5053; 20.281; 21.1684
90; 90; 90
7515.3Zheng, 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 CIFC32 H55 B11 N2P b c a17.474; 20.161; 21.123
90; 90; 90
7441.5Zheng, 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 CIFC26 H43 B11 N2P 21 21 2111.591; 15.516; 16.796
90; 90; 90
3020.7Zheng, 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 CIFC41 H63 B11 N2 OP 21 21 2110.343; 18.963; 22.347
90; 90; 90
4383Zheng, 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 CIFC33 H55 B11 N2P b c a17.5189; 20.3686; 21.3348
90; 90; 90
7613Zheng, 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 CIFC27 H43 B11 N2P 1 21/n 110.2998; 16.7445; 19.7479
90; 101.979; 90
3331.7Zheng, 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 CIFC39 H59 B11 N2P 21 21 2110.4375; 19.3175; 22.8874
90; 90; 90
4614.7Zheng, 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 CIFC20 H23 N3 O2 SP 1 21/n 19.2469; 12.1137; 17.1803
90; 99.893; 90
1895.8Zhu, 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 CIFC25 H25 Br N2 O7P 21 21 2110.943; 12.564; 18.454
90; 90; 90
2537.2Sun, 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 CIFC17 H18 Br N O5P 21 21 216.6023; 7.8736; 32.754
90; 90; 90
1702.7Li, 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 CIFC12 H17 N O4 SP 21 21 218.7741; 9.7409; 14.5365
90; 90; 90
1242.4Riaño, 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 CIFC8 H10 O3P -13.9045; 9.1939; 22.5383
88.422; 88.131; 78.161
791.26Wang, 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 CIFC21 H19 N O3P -18.1086; 8.8324; 13.26
108.838; 97.636; 94.663
883Wang, 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 CIFC77 H89 Br4 Cl3 F8 I4 N4 O8P 4/n c c :218.4165; 18.4165; 27.9044
90; 90; 90
9464.3Beyeh, 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 CIFC72 H114 Br4 Cl2 N4 O9P b c a23.3371; 23.5232; 27.0473
90; 90; 90
14848Beyeh, 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 CIFC7 H7 Cl N O2C 1 2/c 124.849; 4.7231; 14.8643
90; 103.467; 90
1696.6Barnes, 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 CIFC13 H17 N O3P -19.9549; 11.3328; 11.8818
106.461; 101.618; 100.174
1219.6Barnes, 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 CIFC13 H19 N O5P -15.3906; 15.9299; 17.3564
112.457; 97.7331; 99.3952
1326.85Barnes, 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 CIFC15 H11 N O2P -17.1432; 8.4932; 10.1874
99.388; 97.577; 106.771
573.27Chahdoura, 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 CIFC22 H20 N2 O4P 1 21/n 17.0179; 4.6365; 29.074
90; 92.757; 90
944.93Chahdoura, 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 CIFC21 H21 N3 OP 1 c 118.2723; 5.5654; 8.7266
90; 103.633; 90
862.43Chahdoura, 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 CIFC23 H16 OP 1 21 111.008; 7.5883; 19.571
90; 90.988; 90
1634.6Chahdoura, 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 CIFC22 H23 N O2P -19.1264; 9.7169; 10.2731
95.504; 91.157; 101.221
888.78Chahdoura, 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 CIFC20 H18 N4 O2P -15.6257; 19.7469; 23.768
79.737; 88.28; 82.746
2577.3Chahdoura, 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 CIFC20 H13 N O4P -17.1728; 8.0196; 12.8455
84.142; 89.687; 87.901
734.56Chahdoura, 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 CIFC9 H9 N7 OP c a 219.9162; 14.8123; 7.3118
90; 90; 90
1073.97Quinodoz, 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 CIFC15 H13 N O5 SP 3210.3879; 10.3879; 24.218
90; 90; 120
2263.2Quan, 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 CIFC14 H16 O3P -19.017; 12.174; 12.8341
108.889; 99.634; 109.852
1191.34Dethe, 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 CIFC56 H79 B5 O10P 21 21 2112.38928; 20.5595; 23.639
90; 90; 90
6021.26Da 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 CIFC46 H46 B5 Cl3 O10P m n 2120.2644; 13.18215; 8.2499
90; 90; 90
2203.78Da 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 CIFC32 H22 Cl2 SiP 1 21/c 19.959; 24.396; 11.0384
90; 108.602; 90
2541.8Xu, 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 CIFC25 H29 N O3P 21 21 215.572; 15.48; 25.4858
90; 90; 90
2198.3Arena, 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 CIFC23 H16 O3.19P 1 21/c 122.264; 10.1945; 30.92
90; 91.849; 90
7014Liu, 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 CIFC18 H13 N O2P -17.159; 9.364; 10.541
78.846; 82.356; 72.557
659.3Dethe, Dattatraya H.; Kumar B, Vijay
Concise asymmetric total synthesis of bruceolline J
Organic Chemistry Frontiers, 2015, 2, 548
1553102 CIFC30 H24 F12 N6 Ru Sb2P -3 c 110.786; 10.786; 17.286
90; 90; 120
1741.59Gomes, 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 CIFC16 H22 N O3 SP -16.2097; 11.272; 11.547
104.782; 101.238; 100.235
744.1Zhang, 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 CIFC16 H17 N O3 SP -18.3878; 9.8582; 19.139
76.354; 84.421; 73.985
1477.3Zhang, 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 CIFC17 H19 N O3 SP 1 21/c 114.5933; 9.6858; 11.3977
90; 92.745; 90
1609.2Zhang, 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 CIFC33 H30 Br N O5I 2 2 215.713; 28.08; 28.507
90; 90; 90
12578Zhang, 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 CIFC17 H0 I2 N3 O6P 1 21/c 15.5881; 18.985; 10.6706
90; 94.113; 90
1129.13Zhang, 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 CIFC23 H25 N O5P -19.2215; 10.9612; 11.6484
87.764; 69.092; 73.409
1051.48Zhang, 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 CIFC23 H17 I O3C 1 2/c 126.291; 8.781; 18.363
90; 111.863; 90
3934Zhu, 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 CIFC59 H49 Cl4 F6 N P3 RhP 1 21/c 112.3535; 28.8354; 15.2713
90; 99.472; 90
5365.7Chen, 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 CIFC65 H61 F6 N O2 P3 RhP -110.8319; 13.2288; 22.0889
75.156; 79.856; 69.201
2847.44Chen, 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 CIFC59 H46 Cl2 F9 N P3 RhP 1 21/n 113.6534; 25.7008; 15.5862
90; 93.092; 90
5461.29Chen, 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 CIFC58 H52 B Cl6 F4 N O Os P2P 1 21/n 116.5731; 19.6848; 18.1839
90; 112.182; 90
5493.2Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping
Reactions of osmapyridinium with terminal alkynes
Organic Chemistry Frontiers, 2015, 2, 560
1553114 CIFC56.25 H52.25 B Cl2.75 F4 N O3 Os P2P 1 21/c 111.9299; 14.1946; 33.0235
90; 98.576; 90
5529.7Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping
Reactions of osmapyridinium with terminal alkynes
Organic Chemistry Frontiers, 2015, 2, 560
1553115 CIFC50 H43 B Cl5 F4 N3 O Os PP 1 21/c 112.0746; 18.8448; 20.9677
90; 90.023; 90
4771.06Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping
Reactions of osmapyridinium with terminal alkynes
Organic Chemistry Frontiers, 2015, 2, 560
1553116 CIFC52 H55 B Cl4 F4 N3 Os PC 1 c 119.3445; 16.8974; 16.1902
90; 111.004; 90
4940.5Wei, Yuanqing; Zhou, Xiaoxi; Hong, Guangning; Chen, Zhixin; Zhang, Hong; Xia, Haiping
Reactions of osmapyridinium with terminal alkynes
Organic Chemistry Frontiers, 2015, 2, 560
1553117 CIFC19 H21 N O3P 1 21/c 17.2941; 13.2249; 17.2264
90; 96.919; 90
1649.62Santos, 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 CIFC32 H37 N O4 S SnP 1 21 18.592; 10.956; 16.545
90; 92.673; 90
1556Kamimura, 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 CIFC16 H16 Cl I O SP 21 21 217.6495; 12.803; 16.9343
90; 90; 90
1658.5Berthelot-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 CIFC28 H26 Cl P SP 21 21 219.4309; 13.5255; 19.3191
90; 90; 90
2464.3Berthelot-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 CIFC35 H34 Cl3 P Pd SP 21 21 2111.8312; 15.3726; 17.795
90; 90; 90
3236.49Berthelot-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 CIFC19 H20 F3 NP 1 21 110.4422; 33.2582; 10.4466
90; 114.77; 90
3294.2Chen, 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 CIFC23 H35 N S Si TiP 1 21/c 118.029; 9.695; 14.246
90; 110.517; 90
2332.1Suzuki, 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 CIFC23 H35 N S Si ZrP 1 21/c 118.125; 9.87; 14.346
90; 110.563; 90
2402.9Suzuki, 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 CIFC18 H25 N S Si ZrP 1 21/c 115.471; 9.164; 14.06
90; 108.282; 90
1892.8Suzuki, 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 CIFC8 H17 N S SiP -16.2605; 6.9304; 14.4299
92.0278; 99.0665; 112.207
569.305Suzuki, 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 CIFC18 H16 O2 SP 1 21/n 18.3022; 11.1608; 16.3992
90; 94.272; 90
1515.31Chen, 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 CIFC17 H21 N O3P -18.6808; 8.9707; 11.2873
104.818; 112.003; 92.742
777.67Liu, 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 CIFC16 H25 F O2P 21 21 215.9958; 13.644; 17.789
90; 90; 90
1455.3Zhang, Xiaofei; Guo, Shuo; Tang, Pingping
Transition-metal free oxidative aliphatic C‒H fluorination
Organic Chemistry Frontiers, 2015, 2, 806
1553130 CIFC24 H31 F O8P 21 21 218.7359; 12.804; 20.625
90; 90; 90
2307Zhang, Xiaofei; Guo, Shuo; Tang, Pingping
Transition-metal free oxidative aliphatic C‒H fluorination
Organic Chemistry Frontiers, 2015, 2, 806
1553131 CIFC16 H24 Cl2 N2 O PdP 1 21 112.1876; 9.8204; 15.854
90; 96.796; 90
1884.2Yu, Feng; Chen, Pinhong; Liu, Guosheng
Pd(ii)-catalyzed intermolecular enantioselective hydroamination of styrenes
Organic Chemistry Frontiers, 2015, 2, 819
1553132 CIFC2.889 H5.111 N0.222 O0.667 S0.222P 1 21 110.291; 5.9808; 12.068
90; 103.531; 90
722.1Ye, 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 CIFC33 H36 N O8 P SP -110.3564; 12.0563; 14.1956
69.77; 82.139; 68.496
1547.3Kondoh, 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 CIFC11 H13 N O7 S2P 21 21 217.82043; 10.2265; 17.491
90; 90; 90
1398.85Kang, 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 CIFC11 H12 N2 O7 SP 4115.41418; 15.41418; 5.95145
90; 90; 90
1414.05Kang, 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 CIFC14 H14 N2 O3P 1 2/c 112.8276; 8.4882; 24.8068
90; 91.044; 90
2700.6Zhang, 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 CIFC28 H21 F3 N4 O6 Pd2P 1 21/c 114.4863; 17.2032; 11.5651
90; 105.969; 90
2770.93Zhang, 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 CIFC17 H18 N2 O3P -16.8879; 8.282; 14.4023
104.655; 94.121; 91.668
791.85Zhang, 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 CIFC20 H26 N O2 SP -18.6248; 9.8158; 11.6537
99.05; 101.411; 96.596
944.1Pan, 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 CIFC30 H31 N O2 SP 1 21/n 18.5768; 10.2978; 28.986
90; 90.183; 90
2560.1Pan, 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 CIFC21 H22 Br N3 O5P 1 21 19.8915; 9.4814; 11.942
90; 102.048; 90
1095.31Hu, 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 CIFC14 H15 Br N2 O3P n a 217.1573; 21.4898; 9.4975
90; 90; 90
1460.8Hu, 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 CIFC70 H66 Cl34 N8 P2 Ru2P 1 21/n 113.25; 16.9695; 23.3436
90; 103.948; 90
5093.95Mejuto, 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 CIFC32 H35 Cl2 N4 O5 P RuP 1 21/c 118.2792; 11.74106; 17.1049
90; 117.389; 90
3259.49Mejuto, 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 CIFC26 H17 O3 PP 21 21 218.4926; 12.013; 19.248
90; 90; 90
1963.7Xu, 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 CIFC25 H23 Au I N3 OC 1 2/c 132.577; 10.964; 15.077
90; 101.267; 90
5281.3Xu, 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 CIFC23 H19 Au I N3 OP 21 21 2110.3025; 16.0231; 26.3966
90; 90; 90
4357.5Xu, 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 CIFC24 H34 O10P 21 21 215.8507; 14.177; 30.834
90; 90; 90
2557.5Huang, 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 CIFC21 H19 N O6P 21 21 2110.8569; 14.913; 23.1808
90; 90; 90
3753.2Duan, 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 CIFC72 H74 I2 N36 O16P n a 2113.093; 25.621; 27.14
90; 90; 90
9104Zhou, 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 CIFC18 H19 N O2C 1 2/c 120.293; 6.84225; 22.5979
90; 90.8593; 90
3137.36Hama 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 CIFC18 H19 N O2P 1 21/c 17.63367; 29.2305; 6.84862
90; 102.295; 90
1493.12Hama 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 CIFC19 H21 N O2P b c a12.4972; 14.1613; 17.5538
90; 90; 90
3106.61Hama 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 CIFC16 H17 N O3P 21 21 216.86998; 15.21957; 27.0563
90; 90; 90
2828.96Hama 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 CIFC19 H21 N O3P -16.98428; 15.3845; 16.6168
110.497; 97.0023; 102.274
1596.16Hama 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 CIFC18 H20 N2 O3P -16.8071; 15.0202; 15.8559
90.798; 101.156; 100.035
1564.3Hama 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 CIFC11 H14 N2 O2P -17.5414; 11.8446; 12.2635
80.154; 88.093; 88.519
1078.48Hama 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

Left arrow Left arrow First | Left arrow Previous 100 | of 2 | Next 100 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!