بحث البنية الفرعية

14086

CN(C(=O)OC(C)(C)C)C1CCC(C=O)CC1
Reaction #53867
(4-Formyl-cyclohexyl)-methyl-carbamic acid tert-butyl ester
المردود 100.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCCC1CC(=O)OCC(=O)c1ccccc1
Reaction #58451
title compound
المردود 74.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCCC1CC(=O)OCC(=O)c1ccccc1
Reaction #58456
title compound
المردود 95.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1CCCCN1C(=O)OCc1ccccc1)OCC(=O)c1ccccc1
Reaction #58457
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(=O)N(c2cc(-c3cccc(F)c3)sc2C(=O)O)C(C)C)CC1
Reaction #160355
5-(3-Fluoro-phenyl)-3-[isopropyl-(4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1nc(-c2c[nH]c3ncc(Cl)cc23)nc(N[C@H]2CCCC[C@@H]2C(=O)O)c1F
Reaction #162142
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C(=O)O)CCCCC1Nc1nc(-c2c[nH]c3ncc(Cl)cc23)ncc1F
Reaction #162182
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(C(N)=O)CCC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162183
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(N=C=O)CCC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162184
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)O)[C@]1(O)CCC[C@H](Nc2nc(-c3c[nH]c4ncc(F)cc34)ncc2F)C1
Reaction #162190
61d
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@]1(O)CCC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162200
(1S,3S)-3-[[2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoro-pyrimidin-4-yl]amino]-N-ethyl-1-hydroxy-cyclohexanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC2CC(CC(C(=O)O)C2)C1
Reaction #180575
DOI: 10.1039/C8SC04228D
C=C(CC(C(=O)OCC)C1CCN(C(=O)OCc2ccccc2)CC1)C1CC1
Reaction #183045
DOI: 10.1039/C8SC04228D
Cc1cc(COc2ccc(S(=O)(=O)NC3CCCCC3C(=O)NO)cc2)c2ccccc2n1
Reaction #190209
DOI: 10.1039/C8SC04228D
CN(CCO)C(=O)CC1CCN(C(=O)C2NC(CC(C)(C)C)C(C#N)(c3ccc(Cl)cc3F)C2c2cccc(Cl)c2F)CC1
Reaction #192114
DOI: 10.1039/C8SC04228D
Cn1cc(-c2cn(S(=O)(=O)c3ccccc3)c3ncc(C4CCC(C=O)CC4)cc23)cn1
Reaction #200191
DOI: 10.1039/C8SC04228D
O=C1C(O)=C(C2CCC(c3ccc(Cl)cc3)CC2)C(=O)c2ccccc21
Reaction #216207
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cccc(Cn2ncc3c(N4CCN(C(=O)[C@H]5CC[C@H](N6CCCC6)CC5)CC4)ncnc32)c1
Reaction #218433
1-(3-ethoxybenzyl)-4-[4-[[trans-4-(1-pyrrolidinyl)cyclohexyl]carbonyl]piperazin-1-yl]-1H-pyrazolo[3,4-d]-pyrimidine
المردود 71.5%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2cc(-c3ccc4c(c3)CN(C(=O)CC3CCCC3)CC4)nc(N)n2)CC1
Reaction #222523
DOI: 10.1039/C8SC04228D
O=C1C2CCCC(N2)C(=O)N1CCCCc1ccccc1
Reaction #224225
DOI: 10.1039/C8SC04228D
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