An 37 Reaktionen beteiligt

40959

SCCC1c2ccccc2-c2ccccc21
Reaction #293706
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=S(=O)([O-])C(F)(F)F.OCc1cc[n+](CCS)cc1
Reaction #323231
4-Hydroxymethyl-1-(2-mercaptoethyl)pyridinium trifluoromethanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CS(=O)(=O)[O-].Cc1cccc[n+]1CCS
Reaction #323232
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
Cc1cc[n+](CCS)cc1.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #323233
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CS(=O)(=O)[O-].CSc1cc[n+](CCS)cc1
Reaction #323234
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CSc1ccc[n+](CCS)c1.[Cl-]
Reaction #323235
3-Methylthio-1-(2-mercaptoethyl)pyridinium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CS(=O)(=O)[O-].Cc1cccc(C)[n+]1CCS
Reaction #323236
impure title compound
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CCOC(=O)CCCCC1C=CCS1
Reaction #383468
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
SCCC1c2ccccc2-c2ccccc21
Reaction #527531
product
Ausbeute 68.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
CN(SCCCl)C(=O)Nc1ccc(Cl)c(Cl)c1
Reaction #529084
N-(2-chloroethylthio)-N-methyl-N'-(3,4-dichlorophenyl)-urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_08
CS(=O)(=O)[O-].C[N+]1(CCS)CCSCC1
Reaction #572409
thiol
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_08
SCCN1CCN(c2cccc3[nH]ccc23)CC1
Reaction #774766
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Sc1ccc(Oc2ccccc2)cc1
Reaction #1019573
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CCN(CC)CCC(CCS)c1ccncc1
Reaction #1041165
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CS(=O)(=O)[O-].C[N+]1(CCS)CCSCC1
Reaction #1065812
thiol
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_05
CCOC(CC(CCS)c1ccncc1)OCC
Reaction #1296234
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
OCCC(CCS)c1ccncc1
Reaction #1298688
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
SCCN1CCN(c2cccc3[nH]ccc23)CC1
Reaction #1479216
title compound
Ausbeute 43.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_03
O=S(=O)([O-])C(F)(F)F.OCc1ccc[n+](CCS)c1
Reaction #1670694
product
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_11
O=S(=O)([O-])C(F)(F)F.OCc1cc[n+](CCS)cc1
Reaction #1670695
product
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_11
Seite 1Weiter