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c1ccc(CSc2ccncc2)cc1

COc1ccc(CSc2ccncc2C(=O)O)cc1
Reaction #63821
4-(4-methoxybenzylthio)-nicotinic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cnccc1SCc1ccc(OC)cc1
Reaction #63822
Methyl 4-(4-methoxybenzylthio)nicotinate
DOI: 10.6084/m9.figshare.5104873.v1
C[n+]1cc(-c2ccccc2)c(SCc2ccccc2)c(-c2cccc(C(F)(F)F)c2)c1.[Cl-]
Reaction #74864
4-benzylthio-1-methyl-3-phenyl-5-(3-trifluoromethylphenyl)-pyridinium chloride
DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(SCc2ccc(Cl)cc2)cc[nH]1
Reaction #197091
DOI: 10.1039/C8SC04228D
COc1ccc(CNc2ccncc2)c2c1OCC2C
Reaction #199792
DOI: 10.1039/C8SC04228D
Sc1cc(Nc2nc(CCc3ccccc3)cs2)ncc1Br
Reaction #224173
DOI: 10.1039/C8SC04228D
Br
Reaction #243283
DOI: 10.1039/C8SC04228D
COc1ccc(CSc2cc(NC(N)=S)ncc2Br)cc1
Reaction #268250
DOI: 10.1039/C8SC04228D
Clc1cnc2nc(-c3ccc(OCCN4CCOCC4)cc3)[nH]c2c1SCc1ccccc1
Reaction #276313
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #302314
DOI: 10.1039/C8SC04228D
FC(F)(F)c1ccc2c(SCc3ccc(CBr)cc3)ccnc2c1
Reaction #384035
DOI: 10.1039/C8SC04228D
FC(F)(F)c1cc(SCc2ccccc2)ccn1
Reaction #624440
4-(benzylthio)-2-(trifluoromethyl)pyridine
Ausbeute 75.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Sc1ccncc1)c1cccc(Br)c1
Reaction #660078
(3-Bromophenyl)(pyridin-4-ylsulfanyl)acetic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CSc2ccncc2)cc1
Reaction #734681
methyl 4-((4-pyridinylthio)methyl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1cccnc1)N1CCC(=C2c3ccc(Cl)cc3CCc3c(SCc4ccccc4)ccnc32)CC1
Reaction #762095
DOI: 10.1039/C8SC04228D
COc1ccc(CSc2cc(NC(=S)NC(=O)c3ccccc3)ncc2Br)cc1
Reaction #785014
DOI: 10.1039/C8SC04228D
Cc1cc(SCc2ccccc2)cc[n+]1[O-]
Reaction #812994
4-Benzylthio-2-picoline-N-oxide
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1cccnc1)N1CCC(=C2c3ccc(Cl)cc3CCc3c(SCc4ccccc4)ccnc32)CC1
Reaction #927459
title compound
Ausbeute 8.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1cccnc1)N1CCC(=C2c3ccc(Cl)cc3CCc3c(SCc4ccccc4)ccnc32)CC1
Reaction #948926
title compound
Ausbeute 8.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(CSc2cc(Cl)nc3c2ncn3[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)cc1
Reaction #987244
61
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
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