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COc1ccc(CS[C@@H]2CN[C@H](C(N)=O)C2)cc1

COc1ccc(CS[C@@H]2CN[C@H](C(N)=O)C2)cc1
Reaction #5164
title compound
Rendement 97.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(CS[C@H]2C[C@@H](C(N)=O)N(C)C2)c1
Reaction #5165
(2S, 4S)-2-Carbamoyl-4-(3-methoxybenzylthio)-1-methylpyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@H]2C[C@@H](C(N)=O)N(CCF)C2)cc1
Reaction #5166
(2S, 4S)-2-Carbamoyl-4-(4-methoxybenzylthio)-1-(2-fluoroethyl)pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)[C@@H]1C[C@H](SCc2ccc(OC)cc2)CN1C(=O)OC(C)(C)C
Reaction #5169
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)[C@@H]1C[C@H](SCc2ccc(OC)cc2)CN1
Reaction #5170
title compound
Rendement 79.4%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)[C@@H]1C[C@H](SCc2ccc(OC)cc2)CN1C
Reaction #5171
title compound
Rendement 21.1%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)[C@@H]1C[C@H](SCc2ccc(OC)cc2)C[N+]1(C)C.O=S(=O)([O-])F
Reaction #5172
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@H]2C[C@@H](C(=O)N(C)C)N(C(=O)OC(C)(C)C)C2)cc1
Reaction #5174
title compound
Rendement 31.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@@H]2CN[C@H](C(=O)N(C)C)C2)cc1
Reaction #5175
title compound
Rendement 56.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@H]2C[C@@H](C(=O)N(C)C)N(C)C2)cc1
Reaction #5176
title compound
Rendement 26.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@H]2C[C@@H](C(=O)N(C)C)[N+](C)(C)C2)cc1.O=S(=O)([O-])F
Reaction #5182
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[N+]1(C)C[C@@H](SCc2ccc(OC)cc2)C[C@H]1C(=O)N(C)C.O=S(=O)([O-])F
Reaction #5189
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C[C@@H](SCc2ccc(OC)cc2)C[C@H]1C(N)=O
Reaction #5192
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[N+]1(C)C[C@@H](SCc2ccc(OC)cc2)C[C@H]1C(N)=O.O=S(=O)([O-])F
Reaction #5193
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@@H]1C[C@H](SCc2ccc(OC)cc2)CN1C(=O)OC(C)(C)C
Reaction #5196
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@@H]1C[C@H](SCc2ccc(OC)cc2)CN1
Reaction #5197
title compound
Rendement 82.5%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@@H]1C[C@H](SCc2ccc(OC)cc2)CN1CC
Reaction #5198
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@@H]1C[C@H](SCc2ccc(OC)cc2)C[N+]1(C)CC.O=S(=O)([O-])F
Reaction #5199
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C[C@@H](SCc2ccc(OC)cc2)C[C@H]1C(=O)NC
Reaction #5200
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[N+]1(C)C[C@@H](SCc2ccc(OC)cc2)C[C@H]1C(=O)NC.O=S(=O)([O-])F
Reaction #5201
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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