Crystallography Open Database

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7156089 CIFC36 H35 N3 O2C 1 c 114.9636; 12.2439; 33.362
90; 96.5; 90
6073.1Wan, Ying; Wang, Hai-Qing; Xu, Meng-Meng; Mei, Guang-Jian; Shi, Feng
Direct C3-arylations of 2-indolylmethanols with tryptamines and tryptophols via an umpolung strategy.
Organic & biomolecular chemistry, 2018, 16, 1536-1542
7156090 CIFC13 H12 F3 N O2P 1 21/c 17.8606; 8.5158; 18.6068
90; 98.771; 90
1230.96Achary, Raghavendra; Mathi, Gangadhar Rao; Kim, Seulgi; Hwang, Jong Yeon; Kim, Pilho
Grignard-mediated rearrangement of trifluoroacetyl from dihydroisoquinoline enamides to afford tertiary trifluoromethylcarbinols.
Organic & biomolecular chemistry, 2018, 16, 1452-1456
7156091 CIFC15 H15 F3 N2 OP 1 21/n 16.9263; 8.7238; 22.5349
90; 95.292; 90
1355.84Achary, Raghavendra; Mathi, Gangadhar Rao; Kim, Seulgi; Hwang, Jong Yeon; Kim, Pilho
Grignard-mediated rearrangement of trifluoroacetyl from dihydroisoquinoline enamides to afford tertiary trifluoromethylcarbinols.
Organic & biomolecular chemistry, 2018, 16, 1452-1456
7156092 CIFC32 H28 N2P -110.474; 10.511; 13.935
87.432; 75.479; 71.405
1406.6Li, Xiao-Fang; Zhang, Xing-Guo; Hu, Bo-Lun; Zhang, Xiao-Hong
Palladium-catalyzed dimerization of N-aryl propargylamines for the synthesis of 3-vinylquinolines.
Organic & biomolecular chemistry, 2018, 16, 1736-1744
7156093 CIFC26 H21 N OP -19.8683; 10.505; 10.8101
110.935; 95.718; 105.727
983.13Li, Xiao-Fang; Zhang, Xing-Guo; Hu, Bo-Lun; Zhang, Xiao-Hong
Palladium-catalyzed dimerization of N-aryl propargylamines for the synthesis of 3-vinylquinolines.
Organic & biomolecular chemistry, 2018, 16, 1736-1744
7156094 CIFC26 H38 N6 O6 S6C 1 2/c 115.4619; 9.5378; 22.6171
90; 92.5215; 90
3332.2Cholewiak, Agnieszka; Dobrzycki, Łukasz; Jurczak, Janusz; Ulatowski, Filip
Disulphide bond exchange inhibited by air - kinetic and thermodynamic products in a library of macrocyclic cysteine derivatives.
Organic & biomolecular chemistry, 2018, 16, 2411-2420
7156095 CIFC124.4 H156.62 N20 O25.4 S16.2P 21 21 2119.763; 21.594; 33.712
90; 90; 90
14387Cholewiak, Agnieszka; Dobrzycki, Łukasz; Jurczak, Janusz; Ulatowski, Filip
Disulphide bond exchange inhibited by air - kinetic and thermodynamic products in a library of macrocyclic cysteine derivatives.
Organic & biomolecular chemistry, 2018, 16, 2411-2420
7156096 CIFC31 H48 N4 O7P 1 21 112.0777; 21.0362; 14.3712
90; 107.602; 90
3480.3Konda, Maruthi; Jadhav, Rohit G.; Maiti, Sayan; Mobin, Shaikh M.; Kauffmann, Brice; Das, Apurba K.
Understanding the conformational analysis of gababutin based hybrid peptides.
Organic & biomolecular chemistry, 2018, 16, 1728-1735
7156097 CIFC31 H50 N4 O9P 1 21 110.958; 16.851; 18.872
90; 101.84; 90
3410.6Konda, Maruthi; Jadhav, Rohit G.; Maiti, Sayan; Mobin, Shaikh M.; Kauffmann, Brice; Das, Apurba K.
Understanding the conformational analysis of gababutin based hybrid peptides.
Organic & biomolecular chemistry, 2018, 16, 1728-1735
7156098 CIFC112 H199 N16 O28P 1 21 120.8114; 12.8324; 23.6124
90; 100.846; 90
6193.29Konda, Maruthi; Jadhav, Rohit G.; Maiti, Sayan; Mobin, Shaikh M.; Kauffmann, Brice; Das, Apurba K.
Understanding the conformational analysis of gababutin based hybrid peptides.
Organic & biomolecular chemistry, 2018, 16, 1728-1735
7156099 CIFC17 H14 N2 O4 SP 1 21/c 17.6656; 19.475; 10.707
90; 93.755; 90
1595Zeng, Fanxun; Zhang, Letian; Shao, Xusheng; Li, Zhong; Xu, Xiaoyong
Catalyst-free synthesis of thiazolidines via sequential hydrolysis/rearrangement reactions of 5-arylidenethiazolidin-4-ones at room temperature.
Organic & biomolecular chemistry, 2018, 16, 1932-1938
7156100 CIFC25 H22 Co2 O9P -18.576; 9.059; 16.3
81.049; 89.263; 78.661
1226.3Montaña, Ángel M; Ponzano, Stefano; Sanasi, Maria-Filomena; Kociok-Köhn, Gabriele
Synthesis of the 10-oxabicyclo[5.2.1]decane framework present in bioactive natural products.
Organic & biomolecular chemistry, 2018, 16, 1557-1580
7156101 CIFC32 H23 N O2P -18.1795; 11.924; 14.235
108.105; 96.245; 108.712
1215.9Wang, Wenhui; Sun, Jinwei; Hu, Huayou; Liu, Yun
Copper-catalyzed aerobic cyclizations of tetrahydroisoquinolines with bromoketones and alkenes for the synthesis of 5,6-dihydropyrrolo[2,1-a]isoquinolines.
Organic & biomolecular chemistry, 2018, 16, 1651-1658
7156102 CIFC20 H11 Cl N2 O2P -18.8729; 9.3458; 10.6991
68.971; 88.64; 69.793
772.05Zhang, Yan; Liu, Jian-Quan; Wang, Xiang-Shan
An efficient synthesis of 16H-dibenzo[2,3:6,7][1,4]oxazepino[5,4-b]quinazolin-16-ones via an Ullmann reaction catalyzed by CuI.
Organic & biomolecular chemistry, 2018, 16, 1679-1685
7156103 CIFC23 H13 Cl F3 N3 OP -19.584; 9.866; 11.366
80.384; 84.059; 66.028
967.5Donthiboina, Kavitha; Namballa, Hari Krishna; Shaik, Siddiq Pasha; Nanubolu, Jagadeesh Babu; Shankaraiah, Nagula; Kamal, Ahmed
Iodine promoted dual oxidative C(sp<sup>3</sup>)-H amination of 2-methyl-3-arylquinazolin-4(3H)-ones: a facile route to 1,4-diarylimidazo[1,5-a]quinazolin-5(4H)-ones.
Organic & biomolecular chemistry, 2018, 16, 1720-1727
7156104 CIFC13 H8 F3 N O3 SP -14.7875; 10.5072; 14.2488
71.68; 88.646; 76.869
661.76Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156105 CIFC15 H7 F3 O4 SP 1 21/c 112.2391; 8.0497; 13.6415
90; 91.602; 90
1343.45Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156106 CIFC17 H12 O3 SP 1 21/c 19.0948; 20.0144; 7.8362
90; 106.353; 90
1368.7Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156107 CIFC11 H5 F3 O3 SP -18.0423; 8.0926; 9.4378
68.147; 84.221; 72.377
543.3Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156108 CIFC16 H9 Br O2 SP -17.8595; 7.9836; 12.2941
89.939; 74.827; 68.477
688.73Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156109 CIFC12 H4 F6 O2 S2P 1 21/c 14.6767; 19.3071; 14.5648
90; 97.949; 90
1302.47Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156110 CIFC15 H7 F3 O2 SP -17.4794; 7.9785; 11.9788
95.823; 102.31; 113.691
625.39Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156111 CIFC13 H9 F3 O3 SI 1 2/a 114.5769; 11.1576; 31.0437
90; 102.048; 90
4937.8Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156112 CIFC17 H12 O2 SP -17.2227; 8.4064; 12.3348
75.046; 76.516; 66.783
657.64Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156113 CIFC11 H5 F3 O2 SP 1 21/c 119.2151; 7.8797; 7.1525
90; 97.718; 90
1073.14Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156114 CIFC21 H14 O4 SP b c a14.1466; 12.4232; 18.979
90; 90; 90
3335.5Jardim, Guilherme A. M.; Oliveira, Willian X. C.; de Freitas, Rossimiriam P.; Menna-Barreto, Rubem F S; Silva, Thaissa L.; Goulart, Marilia O. F.; da Silva Júnior, Eufrânio N
Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: a new protocol for potent trypanocidal quinones.
Organic & biomolecular chemistry, 2018, 16, 1686-1691
7156115 CIFC20 H20 O5C 1 2 117.823; 6.9975; 27.834
90; 100.799; 90
3409.9Henrion, S.; Macé, A; Vallejos, M. M.; Roisnel, T.; Carboni, B.; Villalgordo, J. M.; Carreaux, F.
Asymmetric synthesis of trans-4,5-disubstituted γ-butyrolactones involving a key allylboration step. First access to (-)-nicotlactone B and (-)-galbacin.
Organic & biomolecular chemistry, 2018, 16, 1672-1678
7156116 CIFC17 H14 Cl N O5P 21 21 217.5946; 13.4938; 15.8269
90; 90; 90
1621.94Maity, Rajendra; Pan, Subhas Chandra
Organocatalytic asymmetric Michael/hemiacetalization/acyl transfer reaction of α-nitroketones with o-hydroxycinnamaldehydes: synthesis of 2,4-disubstituted chromans.
Organic & biomolecular chemistry, 2018, 16, 1598-1608
7156117 CIFC55 H56 N4 O12P 1 21/c 121.1; 23.1109; 23.201
90; 112.784; 90
10430.9Yang, Ya-Fen; Hu, Wei-Bo; Shi, Lei; Li, Sheng-Gang; Zhao, Xiao-Li; Liu, Yahu A.; Li, Jiu-Sheng; Jiang, Biao; Wen, Ke
Guest-regulated chirality switching of planar chiral pseudo[1]catenanes.
Organic & biomolecular chemistry, 2018, 16, 2028-2032
7156118 CIFC61 H68 N4 O12P 1 21/n 111.9894; 21.2887; 21.7173
90; 93.3; 90
5533.9Yang, Ya-Fen; Hu, Wei-Bo; Shi, Lei; Li, Sheng-Gang; Zhao, Xiao-Li; Liu, Yahu A.; Li, Jiu-Sheng; Jiang, Biao; Wen, Ke
Guest-regulated chirality switching of planar chiral pseudo[1]catenanes.
Organic & biomolecular chemistry, 2018, 16, 2028-2032
7156119 CIFC63 H68 N6 O12P b c a20.9082; 23.7424; 23.9838
90; 90; 90
11905.8Yang, Ya-Fen; Hu, Wei-Bo; Shi, Lei; Li, Sheng-Gang; Zhao, Xiao-Li; Liu, Yahu A.; Li, Jiu-Sheng; Jiang, Biao; Wen, Ke
Guest-regulated chirality switching of planar chiral pseudo[1]catenanes.
Organic & biomolecular chemistry, 2018, 16, 2028-2032
7156120 CIFC57 H60 N4 O12P -112.346; 19.5371; 22.8661
106.561; 102.458; 97.147
5059.3Yang, Ya-Fen; Hu, Wei-Bo; Shi, Lei; Li, Sheng-Gang; Zhao, Xiao-Li; Liu, Yahu A.; Li, Jiu-Sheng; Jiang, Biao; Wen, Ke
Guest-regulated chirality switching of planar chiral pseudo[1]catenanes.
Organic & biomolecular chemistry, 2018, 16, 2028-2032
7156121 CIFC61 H68 Cl4 N4 O12P -111.0365; 16.7007; 17.2058
93.872; 92.106; 108.051
3002.8Yang, Ya-Fen; Hu, Wei-Bo; Shi, Lei; Li, Sheng-Gang; Zhao, Xiao-Li; Liu, Yahu A.; Li, Jiu-Sheng; Jiang, Biao; Wen, Ke
Guest-regulated chirality switching of planar chiral pseudo[1]catenanes.
Organic & biomolecular chemistry, 2018, 16, 2028-2032
7156122 CIFC59 H64 N4 O12P 1 21/c 111.5406; 19.4516; 23.9649
90; 101.455; 90
5272.56Yang, Ya-Fen; Hu, Wei-Bo; Shi, Lei; Li, Sheng-Gang; Zhao, Xiao-Li; Liu, Yahu A.; Li, Jiu-Sheng; Jiang, Biao; Wen, Ke
Guest-regulated chirality switching of planar chiral pseudo[1]catenanes.
Organic & biomolecular chemistry, 2018, 16, 2028-2032
7156123 CIFC13 H9 F3 O4 SP 1 21/c 113.1925; 13.3019; 7.7183
90; 100.757; 90
1330.6Wang, Yajun; Wu, Rui; Zhao, Shijun; Quan, Zhengjun; Su, Yingpeng; Huo, Congde
Air promoted annulation of thiophenols with alkynes leading to benzothiophenes.
Organic & biomolecular chemistry, 2018, 16, 1667-1671
7156124 CIFC17 H22 O7P 21 21 218.16871; 8.25025; 23.3395
90; 90; 90
1572.94Zhang, Zhan-Xin; Wu, Pei-Qian; Li, Hui-Hong; Qi, Feng-Ming; Fei, Dong-Qing; Hu, Qiao-Ling; Liu, Ying-Hong; Huang, Xiao-Ling
Norcrassin A, a novel C<sub>16</sub> tetranorditerpenoid, and bicrotonol A, an unusual dimeric labdane-type diterpenoid, from the roots of Croton crassifolius.
Organic & biomolecular chemistry, 2018, 16, 1745-1750
7156125 CIFC40 H68 O4C 1 2 123.0565; 6.6594; 26.3805
90; 117.81; 90
3582.7Zhang, Zhan-Xin; Wu, Pei-Qian; Li, Hui-Hong; Qi, Feng-Ming; Fei, Dong-Qing; Hu, Qiao-Ling; Liu, Ying-Hong; Huang, Xiao-Ling
Norcrassin A, a novel C<sub>16</sub> tetranorditerpenoid, and bicrotonol A, an unusual dimeric labdane-type diterpenoid, from the roots of Croton crassifolius.
Organic & biomolecular chemistry, 2018, 16, 1745-1750
7156126 CIFC26 H22 N2 O3P 1 21 110.4093; 6.2017; 15.4242
90; 92.398; 90
994.84Zhu, Yanshuo; Guo, Jia; Jin, Shaojing; Guo, Jiaomei; Bai, Xuguan; Wang, Qilin; Bu, Zhanwei
Construction of bridged cyclic N,O-ketal spirooxindoles through a Michael addition/N,O-ketalization sequence.
Organic & biomolecular chemistry, 2018, 16, 1751-1759
7156127 CIFC93 H88 N8 O19 S4P 111.3575; 12.9479; 15.7889
81.909; 88.938; 72.873
2196.15Wang, Zhen-Hua; You, Yong; Chen, Yong-Zheng; Xu, Xiao-Ying; Yuan, Wei-Cheng
An asymmetric organocatalytic vinylogous Mannich reaction of 3-methyl-5-arylfuran-2(3H)-ones with N-(2-pyridinesulfonyl) imines: enantioselective synthesis of δ-amino γ,γ-disubstituted butenolides.
Organic & biomolecular chemistry, 2018, 16, 1636-1640
7156128 CIFC18 H20 N4 O3P -18.7419; 10.7719; 10.9487
65.802; 70.156; 75.68
877.51Obydennov, D. L.; Khammatova, L. R.; Eltsov, O. S.; Sosnovskikh, V. Y.
A chemo- and regiocontrolled approach to bipyrazoles and pyridones via the reaction of ethyl 5-acyl-4-pyrone-2-carboxylates with hydrazines.
Organic & biomolecular chemistry, 2018, 16, 1692-1707
7156129 CIFC27 H22 N4 O2P 1 c 18.521; 10.998; 23.489
90; 93.24; 90
2197.7Obydennov, D. L.; Khammatova, L. R.; Eltsov, O. S.; Sosnovskikh, V. Y.
A chemo- and regiocontrolled approach to bipyrazoles and pyridones via the reaction of ethyl 5-acyl-4-pyrone-2-carboxylates with hydrazines.
Organic & biomolecular chemistry, 2018, 16, 1692-1707
7156130 CIFC27 H21 Cl N4 O2P -18.803; 10.863; 12.961
84.4; 71.46; 80.99
1159.1Obydennov, D. L.; Khammatova, L. R.; Eltsov, O. S.; Sosnovskikh, V. Y.
A chemo- and regiocontrolled approach to bipyrazoles and pyridones via the reaction of ethyl 5-acyl-4-pyrone-2-carboxylates with hydrazines.
Organic & biomolecular chemistry, 2018, 16, 1692-1707
7156131 CIFC18 H13 N3P 1 21/n 18.9797; 17.5384; 9.3882
90; 108.488; 90
1402.24Guan, Qianqian; Sun, Qi; Wen, Lixian; Zha, Zhenggen; Yang, Yu; Wang, Zhiyong
The synthesis of benzimidazoles via a recycled palladium catalysed hydrogen transfer under mild conditions.
Organic & biomolecular chemistry, 2018, 16, 2088-2096
7156132 CIFC27 H20 Br N O SeP 1 21/n 113.917; 10.417; 16.611
90; 103.506; 90
2341.6Li, Xiwang; He, Pei; Zhou, Hai-Bing; Dong, Chune
One-step pathway to selenoisobenzofuran-1(3H)-imine derivatives through highly selective selenocyclization of olefinic amides with benzeneselenyl chloride.
Organic & biomolecular chemistry, 2018, 16, 2150-2155
7156133 CIFC19 H13 Cl F3 N3 O2P 1 21/n 15.77529; 22.1018; 14.0999
90; 101.182; 90
1765.61Lim, Bumhee; Park, Seunggun; Park, Jae Hyun; Gam, Jongsik; Kim, Sanghee; Yang, Jung Woon; Lee, Jeeyeon
A metal-free and mild approach to 1,3,4-oxadiazol-2(3H)-ones via oxidative C-C bond cleavage using molecular oxygen.
Organic & biomolecular chemistry, 2018, 16, 2105-2113
7156134 CIFC11 H8 Cl N3 O2P -15.781; 8.5176; 11.7466
102.453; 90.5; 98.113
558.69Lim, Bumhee; Park, Seunggun; Park, Jae Hyun; Gam, Jongsik; Kim, Sanghee; Yang, Jung Woon; Lee, Jeeyeon
A metal-free and mild approach to 1,3,4-oxadiazol-2(3H)-ones via oxidative C-C bond cleavage using molecular oxygen.
Organic & biomolecular chemistry, 2018, 16, 2105-2113
7156135 CIFC21 H29 N3 O3P b c a16.772; 9.0637; 25.832
90; 90; 90
3926.9Wang, Hui; Fang, Bin; Zhou, Le; Li, Di; Kong, Lin; Uvdal, Kajsa; Hu, Zhangjun
A reversible and highly selective two-photon fluorescent "on-off-on" probe for biological Cu<sup>2+</sup> detection.
Organic & biomolecular chemistry, 2018, 16, 2264-2268
7156136 CIFC7 H11 N3 OP 1 21 15.5524; 7.337; 9.871
90; 91.581; 90
402Halder, Joydev; Das, Debabrata; Nanda, Samik
A distinctive transformation based diversity oriented synthesis of small ring carbocycles and heterocycles from biocatalytically derived enantiopure α-substituted-β-hydroxyesters.
Organic & biomolecular chemistry, 2018, 16, 2549-2575
7156137 CIFC26 H32 O3 SiP 1 21 110.523; 10.046; 11.683
90; 103.959; 90
1198.6Halder, Joydev; Das, Debabrata; Nanda, Samik
A distinctive transformation based diversity oriented synthesis of small ring carbocycles and heterocycles from biocatalytically derived enantiopure α-substituted-β-hydroxyesters.
Organic & biomolecular chemistry, 2018, 16, 2549-2575
7156138 CIFC25 H33 N3 O2 SiP 1 21 110.558; 39.473; 11.458
90; 90; 90
4775Halder, Joydev; Das, Debabrata; Nanda, Samik
A distinctive transformation based diversity oriented synthesis of small ring carbocycles and heterocycles from biocatalytically derived enantiopure α-substituted-β-hydroxyesters.
Organic & biomolecular chemistry, 2018, 16, 2549-2575

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