thioacetic acid

CC(=O)SC1CNC(=O)C1
Reaction #5215
4-acetylthio-2-pyrrolidinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1ccc(Cl)cc1CSC(C)=O
Reaction #11764
title compound
المردود 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)S[C@H]1CNC(=O)C1
Reaction #49776
crystalline residue
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COC(=O)c1ccc(CCSC(C)=O)c(C(=O)OC)c1
Reaction #51870
colorless oil
المردود 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccccc1-c1ccc2c(c1)C(CNc1ccccc1)=CC(C)(C)N2
Reaction #54052
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(=O)[C@@H]1CNC(=S)C1
Reaction #64773
(4S)-4-acetylthio-2-pyrrolidone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(=O)SC1CCN(C(C)=NC(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #65293
title compound
المردود 79.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(=O)S[C@H]1C[C@@H](C(=O)N2CCN(CCOC(=O)OCc3ccc([N+](=O)[O-])cc3)CC2)N(C(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #65624
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(=O)S[C@@H]1CC[C@@]2(C)C(C1)[C@@H](O)C[C@H]1[C@@H]3CC[C@H](O)[C@@]3(C)CC[C@@H]12
Reaction #70407
3α-acetylthioandrostane-6α,17β-diol
المردود 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C(C)C(C)SC(C)=O
Reaction #71583
objective compound
المردود 93.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C(C)C(C)SC(C)=O
Reaction #71585
ethyl 3-acetylthio-2-methylbutyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=O)S[C@@H](CC(C)C)C(=O)O
Reaction #74191
title compound
المردود 61.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1c2ccc(Cl)cc2CC1S
Reaction #74907
5-Chloro-2-mercapto-1-indanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CC(=O)SCC(=O)NC/C=C\COc1cc(CN2CCCCC2)ccn1
Reaction #80387
title compound
المردود 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(=O)SCCCC(=O)NC/C=C\COc1cc(CN2CCCCC2)ccn1
Reaction #80399
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(=O)[SH]1C(O)CC[C@H]1CO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
Reaction #83107
desired product
المردود 67.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(=O)SC(CC(=O)c1cnn(C)c1)C(=O)N1CCC[C@H]1C(=O)O
Reaction #94773
1-[2-Acetylthio-3-(1-methyl-4-pyrazolylcarbonyl)propionyl]-L-proline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CC(=O)SC(CC(=O)c1cnn(C)c1)C(=O)N1CCC[C@H]1C(=O)O
Reaction #94796
1-[2-Acetylthio-3-(1-methyl-4-pyrazolylcarbonyl)propionyl]-L-proline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CC(=O)SC(CC(=O)c1cnn(C)c1)C(=O)N1CCC[C@H]1C(=O)O
Reaction #94819
1-[2-Acetylthio-3-(1-methyl-4-pyrazolylcarbonyl)-propionyl]-L-proline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CC(=O)SCCN(CCc1ccccc1)C(=O)NC(CC(C)C)C(=O)N1CCN(C)CC1
Reaction #173878
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
الصفحة 1التالي