potassium thioacetate

CC(=S)C1CCC(C)(C)c2ccc(Br)cc21
Reaction #1317
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CCC3C(C)=S)cc1
Reaction #1338
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOCc1nc2cnc3cc(Br)ccc3c2n1CCCCSC(C)=O
Reaction #9515
thioacetic acid S-[4-(7-bromo-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]ester
المردود 103.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)[C@@H]1C[C@H](SC(C)=O)CN1C
Reaction #10039
title compound
المردود 97.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)S[C@@H](Cc1ccccc1)C(=O)O
Reaction #11024
(2S)-2-acetylthio-3-phenylpropionic acid
المردود 83.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)S[C@@H](Cc1ccccc1)C(=O)O
Reaction #11025
(2S)-2-acetylthio-3-phenylpropionic acid
المردود 94.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)S[C@@H](Cc1ccccc1)C(=O)O
Reaction #11026
(2S)-2-acetylthio-3-phenylpropionic acid
المردود 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)SC[C@H]1CC[C@H](N(C)C(=O)Oc2ccc(Cl)cc2)CC1
Reaction #53850
trans-Thioacetic acid S-{4-[(4-chloro-phenoxycarbonyl)-methyl-amino]-cyclohexylmethyl} ester
المردود 103.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC1(C(=O)O)CSSC1
Reaction #69409
dithiolane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1(C(=O)O)CSSC1
Reaction #70088
dithiolane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(CC(SC(C)=O)C(N)=O)cc1C(=O)NCc1ccc(C(F)(F)F)cc1
Reaction #77811
5-(2-acetylthio-2-carbamoylethyl)-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide
المردود 91.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(=O)S[C@@H](CC(C)(C)C)C(=O)O
Reaction #81087
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(=O)S[C@@H](C)C(=O)O
Reaction #81088
title product
المردود 80.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(=O)S[C@@H]1CO[C@@H](CS(=O)(=O)c2ccc(F)cc2)C1
Reaction #83048
desired product
المردود 55.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(=O)S[C@H]1CO[C@@H](C(=O)N2CCN(C(=O)OCc3ccccc3)CC2)C1
Reaction #83068
desired product
المردود 82.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(=O)SC1COC(c2ccc(F)cc2F)C1
Reaction #83074
desired product
المردود 76.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(=O)SCC1CCOCC1
Reaction #160417
thioacetic acid S-(tetrahydro-pyran-4-ylmethyl)ester
المردود 86.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)SC(C)(C)C(=O)Nc1cc(C(C)(C)C)on1
Reaction #160420
thioacetic acid S-[1-(5-tert-butyl-isoxazol-3-ylcarbamoyl)-1-methyl-ethyl]ester
المردود 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)SCC(=O)c1ccc2c(c1)CCN2S(=O)(=O)c1ccccc1
Reaction #217670
Thioacetic acid S-[2-(1-benzenesulfonyl-2,3-dihydro-1H-indol-5-yl)-2-oxo-ethyl]ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
—
Reaction #304471
solid
المردود 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
الصفحة 1التالي