Crystallography Open Database

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7157080 CIFC50 H52 N4 O4P -112.8963; 13.1501; 17.101
92.305; 111.817; 103.594
2590.69Xu, Yuanshuang; Zhang, Linghua; Liu, Mengyang; Zhang, Xiaopeng; Zhang, Xinying; Fan, Xuesen
Synthesis of benzoazepine derivatives via Rh(iii)-catalyzed inert C(sp<sup>2</sup>)-H functionalization and [4 + 3] annulation.
Organic & biomolecular chemistry, 2019, 17, 8706-8710
7157081 CIFC21 H17 F N2 O2P 21 21 218.7924; 10.9272; 18.098
90; 90; 90
1738.79Xu, Yuanshuang; Zhang, Linghua; Liu, Mengyang; Zhang, Xiaopeng; Zhang, Xinying; Fan, Xuesen
Synthesis of benzoazepine derivatives via Rh(iii)-catalyzed inert C(sp<sup>2</sup>)-H functionalization and [4 + 3] annulation.
Organic & biomolecular chemistry, 2019, 17, 8706-8710
7157082 CIFC21 H16 N2 OP b c a11.2543; 11.6498; 23.6897
90; 90; 90
3105.96Xu, Yuanshuang; Zhang, Linghua; Liu, Mengyang; Zhang, Xiaopeng; Zhang, Xinying; Fan, Xuesen
Synthesis of benzoazepine derivatives via Rh(iii)-catalyzed inert C(sp<sup>2</sup>)-H functionalization and [4 + 3] annulation.
Organic & biomolecular chemistry, 2019, 17, 8706-8710
7157083 CIFC23 H23 Br N2 O3 SP 1 21/c 18.7087; 24.853; 10.406
90; 110.876; 90
2104.4Xu, Yuanshuang; Zhang, Linghua; Liu, Mengyang; Zhang, Xiaopeng; Zhang, Xinying; Fan, Xuesen
Synthesis of benzoazepine derivatives via Rh(iii)-catalyzed inert C(sp<sup>2</sup>)-H functionalization and [4 + 3] annulation.
Organic & biomolecular chemistry, 2019, 17, 8706-8710
7157084 CIFC23 H26 N2 O2P 1 21/n 111.5219; 11.4926; 15.5242
90; 92.72; 90
2053.3Amiri, Kamran; Khosravi, Hormoz; Balalaie, Saeed; Golmohammadi, Farhad; Anwar, Muhammad U.; Al-Harrasi, Ahmed
Regio- and chemo-selective cyclization of allenic-Ugi products for the synthesis of 3-pyrroline skeletons.
Organic & biomolecular chemistry, 2019, 17, 8858-8870
7157085 CIFC25 H26 Cl2 N2 O2P 1 21/n 116.0878; 7.3312; 19.996
90; 101.831; 90
2308.3Amiri, Kamran; Khosravi, Hormoz; Balalaie, Saeed; Golmohammadi, Farhad; Anwar, Muhammad U.; Al-Harrasi, Ahmed
Regio- and chemo-selective cyclization of allenic-Ugi products for the synthesis of 3-pyrroline skeletons.
Organic & biomolecular chemistry, 2019, 17, 8858-8870
7157086 CIFC31 H27 N O4 SP 1 21/c 115.6522; 13.6042; 12.4636
90; 107.449; 90
2531.8Gharpure, Santosh J.; Nanda, Santosh K.; Fartade, Dipak J.
Expeditious diastereoselective synthesis of medium ring heterocycle-fused chromenes via tandem 8/9-endo-dig and 8-exo-dig hydroalkoxylation-formal-[4 + 2] cycloaddition.
Organic & biomolecular chemistry, 2019, 17, 8806-8810
7157087 CIFC56 H58 N2 O10 S2P -110.605; 16.0358; 16.1366
69.467; 72.006; 89.666
2427.91Gharpure, Santosh J.; Nanda, Santosh K.; Fartade, Dipak J.
Expeditious diastereoselective synthesis of medium ring heterocycle-fused chromenes via tandem 8/9-endo-dig and 8-exo-dig hydroalkoxylation-formal-[4 + 2] cycloaddition.
Organic & biomolecular chemistry, 2019, 17, 8806-8810
7157088 CIFC33 H31 N O4 SP 1 21/c 19.2545; 9.0908; 32.563
90; 96.115; 90
2724Gharpure, Santosh J.; Nanda, Santosh K.; Fartade, Dipak J.
Expeditious diastereoselective synthesis of medium ring heterocycle-fused chromenes via tandem 8/9-endo-dig and 8-exo-dig hydroalkoxylation-formal-[4 + 2] cycloaddition.
Organic & biomolecular chemistry, 2019, 17, 8806-8810
7157089 CIFC32 H29 N O4 SP 1 21 19.2331; 9.4073; 15.2033
90; 91.611; 90
1320.01Gharpure, Santosh J.; Nanda, Santosh K.; Fartade, Dipak J.
Expeditious diastereoselective synthesis of medium ring heterocycle-fused chromenes via tandem 8/9-endo-dig and 8-exo-dig hydroalkoxylation-formal-[4 + 2] cycloaddition.
Organic & biomolecular chemistry, 2019, 17, 8806-8810
7157090 CIFC33 H31 N O5 SP 1 21 19.1034; 9.5264; 15.9591
90; 91.547; 90
1383.51Gharpure, Santosh J.; Nanda, Santosh K.; Fartade, Dipak J.
Expeditious diastereoselective synthesis of medium ring heterocycle-fused chromenes via tandem 8/9-endo-dig and 8-exo-dig hydroalkoxylation-formal-[4 + 2] cycloaddition.
Organic & biomolecular chemistry, 2019, 17, 8806-8810
7157091 CIFC52 H50 N2 O8 S2P 1 21/c 18.3119; 24.2166; 11.0613
90; 93.864; 90
2221.4Gharpure, Santosh J.; Nanda, Santosh K.; Fartade, Dipak J.
Expeditious diastereoselective synthesis of medium ring heterocycle-fused chromenes via tandem 8/9-endo-dig and 8-exo-dig hydroalkoxylation-formal-[4 + 2] cycloaddition.
Organic & biomolecular chemistry, 2019, 17, 8806-8810
7157092 CIFC27 H23 N O5P -16.0337; 12.7989; 15.3967
83.2254; 79.7254; 82.5173
1154.49Kurian, Jais; M, Muraleedharan Kannoth
Synthesis of new cyclazines and 4,5-diaryl-1H-pyrrol-3(2H)-one units in discoipyrroles from indolizinone-DMAD cycloadducts.
Organic & biomolecular chemistry, 2019, 17, 8832-8848
7157093 CIFC36 H34 N2 O4P -111.6409; 11.8981; 12.5461
67.133; 76.352; 89.759
1548.5Kurian, Jais; M, Muraleedharan Kannoth
Synthesis of new cyclazines and 4,5-diaryl-1H-pyrrol-3(2H)-one units in discoipyrroles from indolizinone-DMAD cycloadducts.
Organic & biomolecular chemistry, 2019, 17, 8832-8848
7157094 CIFC24 H29 N O6P 1 21/n 19.932; 12.9438; 18.2127
90; 92.2716; 90
2339.55Kurian, Jais; M, Muraleedharan Kannoth
Synthesis of new cyclazines and 4,5-diaryl-1H-pyrrol-3(2H)-one units in discoipyrroles from indolizinone-DMAD cycloadducts.
Organic & biomolecular chemistry, 2019, 17, 8832-8848
7157095 CIFC35 H22 Cl N O4P -110.0137; 11.9245; 12.3604
80.619; 82.259; 67.699
1343Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157096 CIFC28 H15 Br O3P 1 21/c 116.1126; 14.9541; 8.7949
90; 104.805; 90
2048.8Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157097 CIFC34 H19 Cl O3P -17.6023; 14.1593; 14.3949
112.791; 94.3666; 96.6561
1406.45Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157098 CIFC37 H27 Br N2 O3P -111.5199; 11.9192; 12.6746
109.822; 108.543; 99.91
1473.8Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157099 CIFC34 H19 Br O3P -112.672; 14.322; 15.13
80.53; 89.793; 68.279
2511.3Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157100 CIFC38 H30 N2 O3P -111.465; 11.89; 12.656
110.391; 108.863; 98.617
1461.8Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157101 CIFC32 H18 Br N O2P 1 21/c 112.5801; 29.118; 7.2563
90; 98.229; 90
2630.7Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157102 CIFC35 H22 Br N O4P -19.9903; 12.0129; 12.3878
80.372; 82.962; 68.265
1358.56Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157103 CIFC73 H52 Cl2 N2 O8P -111.4707; 17.0265; 17.1384
68.014; 87.526; 70.835
2919.6Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157104 CIFC34 H18 Cl4 O3P 1 21/n 16.8857; 16.5875; 24.9506
90; 93.9567; 90
2842.98Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157105 CIFC34 H19 Br O3P -114.3618; 16.8874; 19.6152
77.2599; 71.5053; 73.2936
4277.2Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157106 CIFC35 H22 O3P -17.4625; 14.4575; 14.4842
111.262; 99.696; 94.536
1418.71Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157107 CIFC26 H46 B2 O4 Se2 Si2P n a 2144.64; 6.5823; 11.7225
90; 90; 90
3444.5Hasegawa, Masashi; Kobayakawa, Kosuke; Nojima, Yuki; Mazaki, Yasuhiro
Synthesis and chiroptical properties of stereogenic cyclic dimers based on 2,2'-biselenophene and [2.2]paracyclophane.
Organic & biomolecular chemistry, 2019, 17, 8822-8826
7157108 CIFC49 H37 Cl3 Se4P 1 21 19.6143; 16.0071; 13.8424
90; 94.363; 90
2124.1Hasegawa, Masashi; Kobayakawa, Kosuke; Nojima, Yuki; Mazaki, Yasuhiro
Synthesis and chiroptical properties of stereogenic cyclic dimers based on 2,2'-biselenophene and [2.2]paracyclophane.
Organic & biomolecular chemistry, 2019, 17, 8822-8826
7157109 CIFC30 H36 Se2 Si2P 21 21 219.4081; 14.8474; 20.854
90; 90; 90
2913Hasegawa, Masashi; Kobayakawa, Kosuke; Nojima, Yuki; Mazaki, Yasuhiro
Synthesis and chiroptical properties of stereogenic cyclic dimers based on 2,2'-biselenophene and [2.2]paracyclophane.
Organic & biomolecular chemistry, 2019, 17, 8822-8826
7157110 CIFC19 H17 N3 O3P 1 21/c 115.3447; 10.116; 10.7205
90; 109.892; 90
1564.82Su, Yiting; Huang, Gaofeng; Ye, Fu; Qiao, Panpan; Ye, Jinxiang; Gao, Yu; Chen, Haijun
Facile access to evodiakine enabled by aerobic copper-catalyzed oxidative rearrangement.
Organic & biomolecular chemistry, 2019, 17, 8811-8815
7157111 CIFC19 H17 N3 O3P 1 21/c 116.6547; 13.5081; 16.2182
90; 117.968; 90
3222.5Su, Yiting; Huang, Gaofeng; Ye, Fu; Qiao, Panpan; Ye, Jinxiang; Gao, Yu; Chen, Haijun
Facile access to evodiakine enabled by aerobic copper-catalyzed oxidative rearrangement.
Organic & biomolecular chemistry, 2019, 17, 8811-8815
7157112 CIFC35 H36 F2 N4 O4 SP 1 21 111.896; 10.6048; 13.5243
90; 109.984; 90
1603.42Zhou, Yuxuan; Ma, Fanghui; Lu, Ping; Wang, Yanguang
Preparation of spiro[imidazolidine-4,3'-indolin]-2'-imines via copper(i)-catalyzed formal [2 + 2 + 1] cycloaddition of 3-diazoindolin-2-imines and triazines.
Organic & biomolecular chemistry, 2019, 17, 8849-8852
7157113 CIFC10 H8 Br N OP -15.6468; 12.0159; 14.1013
81.991; 89.552; 82.145
938.51Xu, Kang; Yang, Ruiqi; Yang, Shuang; Jiang, Cheng; Ding, Zhenhua
Hypervalent iodane mediated reactions of N-acetyl enamines for the synthesis of oxazoles and imidazoles.
Organic & biomolecular chemistry, 2019, 17, 8977-8981
7157114 CIFC12 H11 Br N2 O2P b c a9.93; 9.524; 24.977
90; 90; 90
2362.2Xu, Kang; Yang, Ruiqi; Yang, Shuang; Jiang, Cheng; Ding, Zhenhua
Hypervalent iodane mediated reactions of N-acetyl enamines for the synthesis of oxazoles and imidazoles.
Organic & biomolecular chemistry, 2019, 17, 8977-8981
7157115 CIFC20 H24 N2 O6 S2P 1 21/c 111.026; 15.703; 12.684
90; 98.83; 90
2170.1Xu, Zhong-Qi; Wang, Wen-Bo; Zheng, Lin-Chuang; Li, Lin; Duan, Lili; Li, Yue-Ming
Iodine-mediated aminosulfonylation of alkenyl sulfonamides with sulfonyl hydrazides: synthesis of sulfonylmethyl piperidines, pyrrolidines and pyrazolines.
Organic & biomolecular chemistry, 2019, 17, 9026-9038
7157116 CIFC24 H23 Cl N2 O4 S2P -110.622; 10.722; 11.698
78.63; 78.84; 67.46
1196.1Xu, Zhong-Qi; Wang, Wen-Bo; Zheng, Lin-Chuang; Li, Lin; Duan, Lili; Li, Yue-Ming
Iodine-mediated aminosulfonylation of alkenyl sulfonamides with sulfonyl hydrazides: synthesis of sulfonylmethyl piperidines, pyrrolidines and pyrazolines.
Organic & biomolecular chemistry, 2019, 17, 9026-9038
7157117 CIFC38 H64 N4 O7P 110.0311; 13.762; 14.965
92.146; 95.34; 97.624
2036.1Veeresh, Kuruva; Singh, Manjeet; Gopi, Hosahudya N.
Impact of substituent effects on the design of β-sheet mimetics and β-double helices from (E)-vinylogous γ-amino acid oligomers.
Organic & biomolecular chemistry, 2019, 17, 9226-9231
7157118 CIFC43 H66 N4 O7P -115.784; 15.892; 21.646
72.44; 76.389; 61.814
4534.9Veeresh, Kuruva; Singh, Manjeet; Gopi, Hosahudya N.
Impact of substituent effects on the design of β-sheet mimetics and β-double helices from (E)-vinylogous γ-amino acid oligomers.
Organic & biomolecular chemistry, 2019, 17, 9226-9231
7157119 CIFC43 H54 N2 O7P 1 21 16.2833; 33.99155; 8.90762
90; 107.114; 90
1818.25Kiełczewska, Urszula; Morzycki, Jacek W.; Rárová, Lucie; Wojtkielewicz, Agnieszka
The synthesis of solasodine F-homo-analogues.
Organic & biomolecular chemistry, 2019, 17, 9050-9058
7157120 CIFC36 H49 N O6 SP 1 21 16.41147; 9.65864; 26.39665
90; 91.6151; 90
1633.99Kiełczewska, Urszula; Morzycki, Jacek W.; Rárová, Lucie; Wojtkielewicz, Agnieszka
The synthesis of solasodine F-homo-analogues.
Organic & biomolecular chemistry, 2019, 17, 9050-9058
7157121 CIFC18 H15 N O3 SP -18.5498; 9.8965; 10.498
86.67; 77.284; 65.193
785.94Ansari, Monish Arbaz; Yadav, Dhananjay; Soni, Sonam; Singh, Maya Shankar
Phosphonium ylide catalysis: a divergent diastereoselective approach to synthesize cyclic ketene acetals [thia(zolidines/zinanes)] from β-ketothioamides and dihaloalkanes.
Organic & biomolecular chemistry, 2019, 17, 9151-9162
7157122 CIFC19 H15 F3 N O SP b c a11.2395; 9.4816; 32.652
90; 90; 90
3479.7Ansari, Monish Arbaz; Yadav, Dhananjay; Soni, Sonam; Singh, Maya Shankar
Phosphonium ylide catalysis: a divergent diastereoselective approach to synthesize cyclic ketene acetals [thia(zolidines/zinanes)] from β-ketothioamides and dihaloalkanes.
Organic & biomolecular chemistry, 2019, 17, 9151-9162
7157123 CIFC28 H21 Cl N4 OP 21 21 217.5705; 11.9923; 27.772
90; 90; 90
2521.4Ji, Yan-Ling; Li, He-Ping; Ai, Yue-Yan; Li, Guo; He, Xiang-Hong; Huang, Wei; Huang, Rui-Zhen; Han, Bo
Enantio- and diastereoselective synthesis of spiropyrazolones via an organocatalytic [1 + 2 + 3] multicomponent reaction.
Organic & biomolecular chemistry, 2019, 17, 9217-9225
7157124 CIFC28 H21 Cl N4 OP 21 21 217.6734; 11.9044; 27.0141
90; 90; 90
2467.7Ji, Yan-Ling; Li, He-Ping; Ai, Yue-Yan; Li, Guo; He, Xiang-Hong; Huang, Wei; Huang, Rui-Zhen; Han, Bo
Enantio- and diastereoselective synthesis of spiropyrazolones via an organocatalytic [1 + 2 + 3] multicomponent reaction.
Organic & biomolecular chemistry, 2019, 17, 9217-9225
7157125 CIFC10 H9 F2 N3 OI 1 2/a 115.8495; 10.2381; 13.1866
90; 104.544; 90
2071.2You, Yi; Chen, Yueji; You, Chenhui; Wang, Junwen; Weng, Zhiqiang
Synthesis of 3-(tri/difluoromethyl)-1H-1,2,4-triazol-5(4H)-ones via the cyclization of hydrazinecarboxamides with tri/difluoroacetic anhydride.
Organic & biomolecular chemistry, 2019, 17, 9343-9347
7157126 CIFC30 H24 F9 N9 O3P -18.042; 10.654; 20.098
84.402; 81.612; 85.682
1692.2You, Yi; Chen, Yueji; You, Chenhui; Wang, Junwen; Weng, Zhiqiang
Synthesis of 3-(tri/difluoromethyl)-1H-1,2,4-triazol-5(4H)-ones via the cyclization of hydrazinecarboxamides with tri/difluoroacetic anhydride.
Organic & biomolecular chemistry, 2019, 17, 9343-9347
7157127 CIFC16 H20 B F Fe O2P 1 21/n 113.17; 7.7111; 15.613
90; 105.44; 90
1528.4Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157128 CIFC13 H16 Br F Fe SiP 1 21/c 119.502; 11.7498; 13.23
90; 107.235; 90
2895.5Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157129 CIFC22 H21 B F Fe PP b c a12.4583; 14.7599; 20.49
90; 90; 90
3767.8Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157130 CIFC16 H12 F Fe I SP -17.2; 10.0755; 11.5617
64.721; 78.205; 84.196
742.31Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157131 CIFC10 H7 Br Cl F FeP 1 21/n 16.5459; 10.4479; 15.037
90; 91.505; 90
1028Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157132 CIFC10 H7 F Fe I2P 1 21/c 112.21; 28.6668; 6.6319
90; 100.875; 90
2279.6Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157133 CIFC19 H20 F Fe I S SiP 1 21/c 18.8626; 11.0153; 20.456
90; 98.537; 90
1974.9Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157134 CIFC14 H16 F Fe I O2 SiP 1 21/n 16.7304; 13.738; 17.564
90; 100.433; 90
1597.2Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157135 CIFC26 H26 F Fe I O SiP -18.1302; 10.5516; 14.7688
107.406; 93.634; 98.033
1189.6Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157136 CIFC10 H7 Cl F Fe IP 1 21/c 16.6845; 15.913; 10.315
90; 99.375; 90
1082.6Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157137 CIFC13 H16 Br F Fe SiP 1 21/c 117.276; 6.8553; 12.095
90; 100.988; 90
1406.2Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157138 CIFC21 H24 F Fe I O2 SiP -18.514; 10.875; 11.472
86.069; 84.834; 82.271
1046.5Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157139 CIFC25 H25 F Fe I O P SiP -18.1007; 10.7372; 14.989
108.19; 93.055; 97.786
1220.8Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157140 CIFC14 H16 F Fe I O SiP 1 21/n 16.7234; 12.3647; 18.5635
90; 91.338; 90
1542.8Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157141 CIFC20 H20 F Fe I O S SiP -17.148; 9.9469; 15.3417
108.069; 97.069; 91.763
1026.4Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157142 CIFC19 H18 F N3 O3P 1 21/n 119.0038; 7.304; 25.2096
90; 108.964; 90
3309.26Rao, Madhuri P.; Gunaga, Shubha S.; Zuegg, Johannes; Pamarthi, Rambabu; Ganesh, Madhu
Highly regio- and diastereoselective [3 + 2]-cycloadditions involving indolediones and α,β-disubstituted nitroethylenes.
Organic & biomolecular chemistry, 2019, 17, 9390-9402
7157143 CIFC36 H32 Br2 N6 O6P 1 21/n 115.516; 9.876; 23.035
90; 104.61; 90
3416Rao, Madhuri P.; Gunaga, Shubha S.; Zuegg, Johannes; Pamarthi, Rambabu; Ganesh, Madhu
Highly regio- and diastereoselective [3 + 2]-cycloadditions involving indolediones and α,β-disubstituted nitroethylenes.
Organic & biomolecular chemistry, 2019, 17, 9390-9402
7157144 CIFC46 H45 Br2 N6 O6C 1 2/c 124.8162; 11.0757; 34.2851
90; 100.28; 90
9272.2Rao, Madhuri P.; Gunaga, Shubha S.; Zuegg, Johannes; Pamarthi, Rambabu; Ganesh, Madhu
Highly regio- and diastereoselective [3 + 2]-cycloadditions involving indolediones and α,β-disubstituted nitroethylenes.
Organic & biomolecular chemistry, 2019, 17, 9390-9402
7157145 CIFC27 H24 N2 O5 SP 21 21 218.5917; 13.421; 21.279
90; 90; 90
2453.7Lu, Min; Li, Hong; Zou, Chuncheng; Li, Jianchang; Liu, Chengyu; Sun, Maolin; Ma, Yueyue; Cheng, Ruihua; Ye, Jinxing
Primary amine catalyzed diastereo- and enantioselective Michael reaction of thiazolones and α,β-unsaturated ketones.
Organic & biomolecular chemistry, 2019, 17, 9305-9312
7157147 CIFC25 H24 N2 O2 SP 21 21 219.0518; 12.1315; 18.9731
90; 90; 90
2083.47Luo, Shao-Xiong; Liu, Yanzhou; Lambrecht, Michael J.; Ortwine, Daniel F.; DiPasquale, Antonio G.; Liang, Jun; Wang, Xiaojing; Zbieg, Jason R.; Li, Jun
cis-Selective synthesis of 1,3-disubstituted tetrahydro-β-carbolines from N-sulfonyl N,S-acetals.
Organic & biomolecular chemistry, 2019, 17, 9510
7157148 CIFC23 H26 N2 O3 SP 21 21 219.2149; 11.3488; 19.7251
90; 90; 90
2062.81Luo, Shao-Xiong; Liu, Yanzhou; Lambrecht, Michael J.; Ortwine, Daniel F.; DiPasquale, Antonio G.; Liang, Jun; Wang, Xiaojing; Zbieg, Jason R.; Li, Jun
cis-Selective synthesis of 1,3-disubstituted tetrahydro-β-carbolines from N-sulfonyl N,S-acetals.
Organic & biomolecular chemistry, 2019, 17, 9510
7157149 CIFC22 H18 N2 SP 1 21/c 19.6081; 15.136; 11.7745
90; 101.041; 90
1680.65Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157150 CIFC28 H20 N4 O4 SP 1 21/c 113.0978; 8.4281; 21.7783
90; 103.164; 90
2340.92Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157151 CIFC22 H14 N2 OP 1 n 18.7248; 8.5852; 11.534
90; 105.252; 90
833.5Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157152 CIFC40 H30 N8 O S2P -19.4466; 9.9176; 19.5777
79.604; 86.538; 70.029
1695.59Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157153 CIFC24 H16 N2 O4 SP -18.8175; 10.9212; 10.9295
76.676; 67.685; 89.692
943.5Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157154 CIFC22 H16 N2 SeP 1 21/c 19.6424; 15.1758; 11.7826
90; 101.61; 90
1688.9Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157155 CIFC22 H14 F2 N2 SP 1 21/c 19.5114; 15.691; 11.5516
90; 98.966; 90
1702.9Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157156 CIFC72 H60 N6 Se3P -111.8825; 12.7306; 20.6914
90.924; 101.853; 111.378
2838.3Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157157 CIFC16 H13 N O2 SP -16.4036; 7.8241; 14.538
85.37; 89.441; 70.995
686.3You, Guirong; Xi, Dan; Sun, Jian; Hao, Liqiang; Xia, Chengcai
Transition-metal- and oxidant-free three-component reaction of quinoline N-oxides, sodium metabisulfite and aryldiazonium tetrafluoroborates via a dual radical coupling process.
Organic & biomolecular chemistry, 2019, 17, 9479
7157158 CIFC25 H28 N2 O3P 1 21/n 113.4238; 10.0908; 16.9778
90; 96.486; 90
2285.04He, Yi; Narmon, Thomas; Wu, Danjun; Li, Zhenghua; Van Meervelt, Luc; Van der Eycken, Erik V.
A gold-triggered dearomative spirocarbocyclization/Diels-Alder reaction cascade towards diverse bridged N-heterocycles.
Organic & biomolecular chemistry, 2019, 17, 9529
7157159 CIFC24 H26 N2 O3P -111.7236; 11.754; 17.2404
73.252; 73.789; 71.074
2106.24He, Yi; Narmon, Thomas; Wu, Danjun; Li, Zhenghua; Van Meervelt, Luc; Van der Eycken, Erik V.
A gold-triggered dearomative spirocarbocyclization/Diels-Alder reaction cascade towards diverse bridged N-heterocycles.
Organic & biomolecular chemistry, 2019, 17, 9529
7157181 CIFC24 H36 Cl N3 O Pd SeR -3 :H27.319; 27.319; 19.5324
90; 90; 120
12624.5Sharma, Kamal Nayan; Satrawala, Naveen; Srivastava, Avinash Kumar; Ali, Munsaf; Joshi, Raj Kumar
Palladium(ii) ligated with a selenated (Se, C<sub>NHC</sub>, N<sup>-</sup>)-type pincer ligand: an efficient catalyst for Mizoroki-Heck and Suzuki-Miyaura coupling in water.
Organic & biomolecular chemistry, 2019, 17, 8969-8976
7157182 CIFC25 H21 N O3P 1 21/c 111.065; 11.521; 15.832
90; 97.78; 90
1999.68Zeng, Qian; Dong, Kuiyong; Huang, Jingjing; Qiu, Lihua; Xu, Xinfang
Copper-catalyzed carbene/alkyne metathesis terminated with the Buchner reaction: synthesis of dihydrocyclohepta[b]indoles.
Organic & biomolecular chemistry, 2019, 17, 2326-2330
7157183 CIFC29 H22 N2 O3 SP -112.875; 13.03; 15.195
76.583; 78.566; 72.177
2338.2Kundal, Sandip; Chakraborty, Baitan; Paul, Kartick; Jana, Umasish
Efficient two-step synthesis of structurally diverse indolo[2,3-b]quinoline derivatives.
Organic & biomolecular chemistry, 2019, 17, 2321-2325
7157184 CIFC19 H16 N2 SP 1 21/n 18.5086; 17.1346; 22.5907
90; 99.192; 90
3251.2Zhang, Xi; Wang, Tong-Lin; Liu, Xiao-Jun; Wang, Xi-Cun; Quan, Zheng-Jun
The solvent-controlled chemoselective construction of C-S/S-S bonds via the Michael reaction/thiol coupling of quinoline-2-thiones.
Organic & biomolecular chemistry, 2019, 17, 2379-2383
7157185 CIFC14 H15 F6 N3 OP 1 21/n 111.79; 7.792; 16.696
90; 103.74; 90
1489.9Moraes, Paulo A.; Lobo, Marcio M.; Marangoni, Mário A; Meyer, Alexandre R.; Frizzo, Clarissa P.; Bonacorso, Helio G.; Martins, Marcos A. P.; Zanatta, Nilo
Chemo- and regioselective reactions of 5-bromo enones/enaminones with pyrazoles.
Organic & biomolecular chemistry, 2019, 17, 2384-2392
7157186 CIFC14 H17 F6 N3 OP b c a11.65; 18.43; 15.238
90; 90; 90
3272Moraes, Paulo A.; Lobo, Marcio M.; Marangoni, Mário A; Meyer, Alexandre R.; Frizzo, Clarissa P.; Bonacorso, Helio G.; Martins, Marcos A. P.; Zanatta, Nilo
Chemo- and regioselective reactions of 5-bromo enones/enaminones with pyrazoles.
Organic & biomolecular chemistry, 2019, 17, 2384-2392
7157187 CIFC24 H24 Br2 O5P 21 21 2117.353; 24.435; 5.4165
90; 90; 90
2296.7Shit, Sudip; Devi, Namita; Devi, Ngangbam Renubala; Saikia, Anil K.
Stereoselective synthesis of hexahydrofuro[3,4-b]furan-4-ol and its dimer via tandem Prins and pinacol rearrangement.
Organic & biomolecular chemistry, 2019, 17, 7398-7407
7157188 CIFC12 H13 Br O3P 1 21 15.845; 7.6852; 12.8843
90; 100.457; 90
569.15Shit, Sudip; Devi, Namita; Devi, Ngangbam Renubala; Saikia, Anil K.
Stereoselective synthesis of hexahydrofuro[3,4-b]furan-4-ol and its dimer via tandem Prins and pinacol rearrangement.
Organic & biomolecular chemistry, 2019, 17, 7398-7407
7157189 CIFC32 H32 N2 O7P 21 21 2113; 13.405; 17.492
90; 90; 90
3048Sharma, Arun; Sharma, Vivek; Chimni, Swapandeep Singh
Organocatalytic enantioselective conjugate addition of pyrazolin-5-ones to arylomethylidene malonates.
Organic & biomolecular chemistry, 2019, 17, 9514
7157225 CIFC24 H24 N4 O2P -19.145; 11.501; 11.649
117.55; 94.48; 91.05
1080.9Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios
Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones.
Organic & biomolecular chemistry, 2019, 17, 9585-9604
7157226 CIFC17 H12 O5 S2P 1 21/c 18.7498; 18.5113; 9.4511
90; 99.3488; 90
1510.46Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios
Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones.
Organic & biomolecular chemistry, 2019, 17, 9585-9604
7157227 CIFC23 H23 N3 O2I 41/a :238.315; 38.315; 5.547
90; 90; 90
8143.2Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios
Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones.
Organic & biomolecular chemistry, 2019, 17, 9585-9604
7157228 CIFC23 H25 N O4 SP 1 21/n 111.6856; 14.0485; 13.2869
90; 96.0216; 90
2169.2Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios
Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones.
Organic & biomolecular chemistry, 2019, 17, 9585-9604
7157229 CIFC22 H16 O3 SP 1 21/n 18.8058; 20.394; 9.6437
90; 99.794; 90
1706.6Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios
Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones.
Organic & biomolecular chemistry, 2019, 17, 9585-9604
7157230 CIFC24 H23 N O3 SP 1 21/n 19.6018; 12.4113; 16.8115
90; 96.978; 90
1988.6Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios
Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones.
Organic & biomolecular chemistry, 2019, 17, 9585-9604

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