thiolacetic acid

CC(=O)SCC1CCCCCCC(CC(=O)OC(C)(C)C)C(=O)N1
Reaction #5500
10-(acetylthiomethyl)-3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(Cc1cccs1)NCCCSc1ccncc1
Reaction #6218
desired compound
Ausbeute 86.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)C1CC(=S)N(C(C)=O)C1
Reaction #50015
(±)-1-acetyl-4-acetylthio-2-pyrrolidone
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(=O)SCC1CCCCCCC(CC(=O)OC(C)(C)C)C(=O)N1
Reaction #50255
10-(acetylthiomethyl)-3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COC(=O)C[C@H](C)SC(C)=O
Reaction #50704
title compound
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCC(NC(=O)Cc1cccs1)C(=O)OCC(C)C
Reaction #51371
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCCn1c(=O)c2[nH]c(Cc3cccs3)nc2n(CCc2ccc([N+](=O)[O-])cc2)c1=O
Reaction #58146
3-[2-(4-nitrophenyl)ethyl]-1-propyl-8-[(thiophen-2-yl)methyl]xanthine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCCCc1ncc(/C=C(\C(=O)O)c2cccs2)n1Cc1ccccc1Cl
Reaction #65255
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCC(NC(=O)Cc1cccs1)C(=O)OCC(C)C
Reaction #201195
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCN(C(=O)Cc1cccs1)C1CCc2cccc(OC)c2C1
Reaction #212463
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CCCCCCCCCCCCCCCS
Reaction #217463
desired product
Ausbeute 97.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
OCCCCCCCCCCCCCCCCS
Reaction #217465
desired product
Ausbeute 70.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
O=C(O)CCCCCCCCCCCCCCCS
Reaction #217470
desired product
Ausbeute 97.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
OCCCCCCCCCCCCCCCCS
Reaction #217472
desired product
Ausbeute 70.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
O=C(O)CCCCCCCCCCCCCCCS
Reaction #218254
desired product
Ausbeute 97.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
OCCCCCCCCCCCCCCCCS
Reaction #218256
desired product
Ausbeute 70.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCC(NC(=O)Cc1cccs1)C(=O)OCC(C)C
Reaction #220558
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
O=C(O)Cc1ccc(C(=O)c2ccc(Cl)cc2)s1
Reaction #245199
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(Cc1ccccc1)(C(=O)O)c1cccs1
Reaction #246923
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)NCOC(=O)Cc1cccs1
Reaction #250134
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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