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660723

CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC(C)C)C2)nc1C(=O)NCCOC
Reaction #72020
title compound
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1ccc(-c2nc(C(=O)N(C)C)c(C(=O)OCC)s2)cn1
Reaction #178609
DOI: 10.1039/C8SC04228D
CCOC(=O)c1sc(Cl)nc1C
Reaction #187218
DOI: 10.1039/C8SC04228D
CCCCNc1nc(C(F)(F)F)c(C(=O)OCc2ccccc2)s1
Reaction #189721
DOI: 10.1039/C8SC04228D
CCOC(=O)c1sc(OCC)nc1C(F)(F)F
Reaction #189860
DOI: 10.1039/C8SC04228D
CC(C)(C)Nc1nc(C(F)(F)F)c(C(=O)OCc2ccccc2)s1
Reaction #197187
DOI: 10.1039/C8SC04228D
O=C(O)c1sc(Cl)nc1C(F)(F)F
Reaction #204309
DOI: 10.1039/C8SC04228D
O=C(O)c1sc(Cl)nc1-c1ccccc1
Reaction #208266
DOI: 10.1039/C8SC04228D
CCOC(=O)c1sc(Cl)nc1-c1ccc(F)cc1
Reaction #246824
DOI: 10.1039/C8SC04228D
CCOC(=O)c1sc(N=[N+]=[N-])nc1-c1ccc(C(F)(F)F)cc1
Reaction #248729
DOI: 10.1039/C8SC04228D
OCc1sc(Cl)nc1C(F)(F)F
Reaction #271509
DOI: 10.1039/C8SC04228D
N#Cc1cccc(-c2nc(Cl)sc2C(=O)O)c1
Reaction #283195
DOI: 10.1039/C8SC04228D
O=C(O)c1sc(Cl)nc1-c1ccccc1
Reaction #283215
DOI: 10.1039/C8SC04228D
CCOC(=O)c1sc(-n2cnc3cc(OC)c(OC)cc32)nc1-c1ccccc1
Reaction #284765
DOI: 10.1039/C8SC04228D
CCOC(=O)c1sc(Cl)nc1-c1ccc([N+](=O)[O-])cc1
Reaction #298150
DOI: 10.1039/C8SC04228D
CCOC(=O)c1sc(Sc2ccccc2)nc1C
Reaction #312959
ethyl 4-methyl-2-phenylsulfanylthiazole-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(C)=O)=C(N)C(F)(F)C(F)(F)F
Reaction #366923
ethyl 2-acetyl-3-amino-4,4,5,5,5-pentafluoro-2-pentenoate
Rendimiento 37.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1sc(Cl)nc1C(F)(F)F
Reaction #366927
2-chloro-trifluoromethyl-5 thiazolecarboxylic acid
Rendimiento 73.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(Cl)nc1CC
Reaction #366928
yellow liquid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CCC(c3cc(Cl)c(Cl)c(Cl)c3)(C(F)(F)F)C2)nc1C(F)(F)F
Reaction #373796
DOI: 10.1039/C8SC04228D
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