بحث البنية الفرعية

383903

C#CC1(NS(=O)(=O)Cc2ccc(Cl)cc2)CCCCC1
Reaction #192983
DOI: 10.1039/C8SC04228D
O=C(O)COc1c(C(=O)O)sc(-c2cccc(NC3CCN(S(=O)(=O)Cc4cc(Cl)cc(Cl)c4)CC3)c2)c1Br
Reaction #193052
DOI: 10.1039/C8SC04228D
CCCCN1C(=O)C(Cl)=C(c2ccc(Cl)cc2)S1(=O)=O
Reaction #380680
DOI: 10.1039/C8SC04228D
CN([C@H]1CC[C@@]2(O)[C@H]3Cc4ccc(O[Si](C)(C)C(C)(C)C)c5c4[C@@]2(CCN3CC2CC2)[C@H]1O5)S(=O)(=O)Cc1ccc(Cl)c(Cl)c1
Reaction #517889
target compound
المردود 78.3%DOI: 10.6084/m9.figshare.5104873.v1
CN([C@H]1CC[C@@]2(O)[C@H]3Cc4ccc(O[Si](C)(C)C(C)(C)C)c5c4[C@@]2(CCN3CC2CC2)[C@H]1O5)S(=O)(=O)Cc1ccc(Cl)c(Cl)c1
Reaction #654615
target compound
المردود 78.3%DOI: 10.6084/m9.figshare.5104873.v1
CN([C@H]1CC[C@@]2(O)[C@H]3Cc4ccc(O[Si](C)(C)C(C)(C)C)c5c4[C@@]2(CCN3CC2CC2)[C@H]1O5)S(=O)(=O)Cc1ccc(Cl)c(Cl)c1
Reaction #738233
target compound
المردود 78.3%DOI: 10.6084/m9.figshare.5104873.v1
O=S1(=O)NC2(CCCC2)C(CNCCF)=C1c1ccc(Cl)cc1
Reaction #769361
DOI: 10.1039/C8SC04228D
CCCCNS(=O)(=O)Cc1ccc(Cl)cc1
Reaction #816436
title compound
المردود 93.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1C(=O)C(O)=C(c2ccc(Cl)cc2)S1(=O)=O
Reaction #816437
title compound
المردود 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1C(=O)C(Cl)=C(c2ccc(Cl)cc2)S1(=O)=O
Reaction #816438
title compound
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1C(=O)C(Nc2ccc(OC(F)F)cc2)=C(c2ccc(Cl)cc2)S1(=O)=O
Reaction #816462
title compound
المردود 45.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S1(=O)NC2(CCCC2)C(CNCCF)=C1c1ccc(Cl)cc1
Reaction #834575
title intermediate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCNS(=O)(=O)Cc1ccc(Cl)cc1
Reaction #1223833
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCN2C[C@@H](NS(=O)(=O)Cc3ccc(Cl)cc3)C[C@H]2C1
Reaction #1271738
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#CC1(NS(=O)(=O)Cc2ccc(Cl)cc2)CCCCC1
Reaction #1332464
4-chlorophenyl-N-(1-ethynylcyclohexyl)methane-sulfonamide
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(c2ccc(Cl)cc2)S(=O)(=O)N(C)C12CCCCC2
Reaction #1332465
3-(4-chlorophenyl)-1,4-dimethyl-2-thia-1-azaspiro[4.5]dec-3-ene 2,2-dioxide
المردود 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(c2ccc(Cl)cc2)SNC12CCCCC2
Reaction #1332466
3-(4-chlorophenyl)-4-methyl-2-thia-1-azaspiro[4.5]dec-3-ene
المردود 71.1%DOI: 10.6084/m9.figshare.5104873.v1
CNCC1=C(c2ccc(Cl)cc2)S(=O)(=O)NC12CCCCC2
Reaction #1332467
3-(4-Chlorophenyl)-4-methylaminomethyl-2-thia-1-azaspiro[4.5]dec-3-ene 2,2-dioxide
المردود 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CN([C@H]1CC[C@@]2(O)[C@H]3Cc4ccc(O[Si](C)(C)C(C)(C)C)c5c4[C@@]2(CCN3CC2CC2)[C@H]1O5)S(=O)(=O)Cc1ccc(Cl)c(Cl)c1
Reaction #1944641
target compound
المردود 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCC1=C(c2ccc(Cl)cc2)S(=O)(=O)NC12CCCCC2
Reaction #2209960
DOI: 10.1039/C8SC04228D
الصفحة 1التالي