بحث البنية الفرعية

7081

CC(C)NCCS(=O)c1ccc(Cl)cc1
Reaction #4284
solid
المردود 90.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCCS(=O)(=O)c1ccc(Cl)c(Cl)c1
Reaction #4291
white crystalline product
المردود 32.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCCS(=O)(=O)c1ccc(F)cc1.Cl
Reaction #4293
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCCS(=O)(=O)c1ccc(Cl)cc1.Cl
Reaction #4296
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NCCS(=O)c1ccccc1.O=C(O)/C=C\C(=O)O
Reaction #4304
white solid
المردود 177.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(CCS(=O)(=O)c1ccccc1)C(=O)NCCN(C)CCc1ccccc1.CC(C)N(CCS(=O)(=O)c1ccccc1)C(=O)NCCN(C)CCc1ccccc1.O
Reaction #4310
N-(1-Methylethyl)-N'-[2-[methyl-(2-phenylethyl)amino]ethyl]-N-[2-(phenylsulfonyl)ethyl]urea hemihydrate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(CCS(=O)(=O)c1ccccc1)C(=O)NCCN(C)Cc1ccccc1
Reaction #4311
N-(1-Methylethyl)-N'-[2-[methyl(phenylmethyl)amino]ethyl]-N-[2-(phenylsulfonyl)ethyl]urea
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(CCS(=O)(=O)c1ccccc1)C(=O)NCCCN1CCCCC1
Reaction #4318
oil
المردود 27.1%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCNC(=O)N(CCS(=O)c1ccccc1)C(C)C
Reaction #4319
oil
المردود 55.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(C)C)C1Cc2c(-c3ccccc3)cccc2S(=O)C1
Reaction #65939
3-(N-Isopropyl-N-n-propylamino)-5-phenyl-1-oxothiochroman
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@@H]1C[C@H](C#N)CN1C(=O)OCc1ccccc1
Reaction #78415
desired product
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@@H]1C[C@H](C#N)CN1C(=O)OCc1ccccc1
Reaction #78418
desired product 6
المردود 69.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=S1(=O)CCN2c3c(cccc31)[C@@H]1CNCC[C@@H]12
Reaction #79314
title compound
المردود 73.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S1CCN2c3c(cccc31)[C@H]1CNCC[C@H]12
Reaction #79315
title compound
المردود 35.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc3c4c(c2)S(=O)(=O)CCN4[C@H]2CCN(C(=O)OC(C)(C)C)C[C@@H]32)c(C(F)(F)F)c1
Reaction #79316
tert-butyl(6bR,10aS)-5-[4-methoxy-2-(trifluoromethyl)phenyl]-1,2,6b,9,10,10a-hexahydropyrido[4,3-b][1,4]thiazino[2,3,4-hi]indole-8(7H)-carboxylate 3,3-dioxide
المردود 74.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@H]2[C@@H](C1)c1cc(-c3ccc(Cl)cc3Cl)cc3c1N2CCS3(=O)=O
Reaction #79317
Tert-butyl(6bR,10aS)-5-(2,4-dichlorophenyl)-1,2,6b,9,10,10a-hexahydropyrido[4,3-b][1,4]thiazino[2,3,4-hi]indole-8(7H)-carboxylate 3,3-dioxide
المردود 88.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=S1(=O)CCN2c3c(cc(-c4ccc(Cl)cc4Cl)cc31)[C@@H]1CNCC[C@@H]12
Reaction #79318
title compound
المردود 162.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(CCS(=O)(=O)c1ccccc1)C(=O)NCCN(C)Cc1ccccc1
Reaction #206341
DOI: 10.1039/C8SC04228D
Cc1cc(N2CC(S(=O)(=O)c3ccccc3Cl)CC2C(=O)O)n(C2CCCCC2)n1
Reaction #210965
DOI: 10.1039/C8SC04228D
CCCN(C(C)C)C1Cc2c(-c3ccccc3)cccc2S(=O)C1
Reaction #211341
DOI: 10.1039/C8SC04228D
الصفحة 1التالي