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1123930

COC(=O)C1CC(SCc2ccc(OC)cc2)CN1C(=O)OC(C)(C)C
Reaction #5178
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](SCc2ccc(OC)cc2)CN1
Reaction #5179
title compound
Выход 85.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@H]2C[C@@H](C(=O)N3CCN(CCOC(N)=O)CC3)N(C(=O)OCc3ccc([N+](=O)[O-])cc3)C2)cc1
Reaction #65618
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(NC(=O)c2ccccc2C)ccc1C(=O)N1CCCC(OC(=O)[C@H](CCSC)NC(=O)OC(C)(C)C)c2cc(Cl)ccc21
Reaction #83024
5-(N-tert-butoxycarbonyl-L-methionyloxy)-7-chloro-1-[2-methoxy-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzo-azepine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CSC2CC(C(=O)N(C)OC)N(C(=O)OC(C)(C)C)C2)cc1
Reaction #204377
DOI: 10.1039/C8SC04228D
Cc1cc(N2CC(S(=O)(=O)c3ccccc3Cl)CC2C(=O)O)n(C2CCCCC2)n1
Reaction #210965
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C1CC(S(=O)(=O)c2ccccc2)C(c2ccccc2F)N1C(=O)CNC(=O)Nc1cccc(CC(=O)O)c1
Reaction #213015
DOI: 10.1039/C8SC04228D
CC[C@H](C)[C@H](NC(=O)[C@H](C(C)C)N1CCCC1=O)C(=O)N[C@@H](CCSC)C(=O)O
Reaction #216577
N-[2(S)-(pyrrolidin-2-on-1-yl)-3-methylbutanoyl]-isoleucyl-methionine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N2CC(S(C)(=O)=O)CC2C(=O)O)n(-c2ccc(C(F)(F)F)cc2)n1
Reaction #223188
DOI: 10.1039/C8SC04228D
COC(=O)C1(NC(=O)c2cnn3c(-c4ccc(Cl)cc4F)c(-c4ccccc4Cl)cnc23)CCS(=O)(=O)CC1
Reaction #224067
DOI: 10.1039/C8SC04228D
Cc1cc(N2CC(S(=O)(=O)c3ccccc3C(F)(F)F)CC2C(=O)O)n(C(C)C)n1
Reaction #230980
DOI: 10.1039/C8SC04228D
CSCCC(NC(=O)C(Cc1ccc(OC(C)(C)C)cc1)N(C)C(=O)OC(C)(C)C)C(=O)NCCCc1ccccc1
Reaction #231776
DOI: 10.1039/C8SC04228D
COc1ccc(CSC2CC(C(=O)N(C)OC)N(C(=O)OC(C)(C)C)C2)cc1
Reaction #233829
DOI: 10.1039/C8SC04228D
CSCCC(NC(=O)C(Cc1ccccc1)NC(=O)CN(C)C(=O)CNC(=O)C(Cc1ccc(O)cc1)NC(=O)OC(C)(C)C)C(=O)OCc1ccccc1
Reaction #242979
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)N(Cc2ccccc2)C2(C(=O)NO)CCSCC2)cc1
Reaction #253020
DOI: 10.1039/C8SC04228D
CC(C)(ON=C(C(=O)NC1C(=O)N2C1CSC1CC(=O)OC12C(=O)[O-])c1csc(N)n1)C(=O)O
Reaction #273149
DOI: 10.1039/C8SC04228D
COC(=O)C1CC(SCc2ccc(OC)cc2)CN1
Reaction #289315
DOI: 10.1039/C8SC04228D
CC(=O)Nc1ccc(S(=O)(=O)C2CC(C(=O)OC(C)(C)C)N(C(=O)CNC(=O)Nc3cccc(C(=O)O)c3)C2c2ccccc2F)cc1
Reaction #294404
DOI: 10.1039/C8SC04228D
NC(=O)[C@@H](N)CCSC(F)(F)F
Reaction #339875
trifluoromethionine amide
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](CCSC(F)(F)F)C(=O)Nc1ccccc1
Reaction #339876
product
Выход 67.6%DOI: 10.6084/m9.figshare.5104873.v1
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