(r)-(+)-2-methyl-2-propanesulfinamide

CC(C)(C)[S@@](=O)/N=C/CC1(O[Si](C)(C)C(C)(C)C)CC1
Reaction #48289
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)[S@@](=O)/N=C\c1ccc(Br)cc1Cl
Reaction #68558
(R,Z)—N-(4-bromo-2-chlorobenzylidene)-2-methylpropane-2-sulfinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)[S@@](=O)/N=C/c1cc(-c2ccc(Cl)cc2)on1
Reaction #85694
(R,E)-N-((5-(4-chlorophenyl)isoxazol-3-yl)methylene)-2-methylpropane-2-sulfinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)[S@@](=O)/N=C/c1ccc(Br)cc1F
Reaction #85696
(R,E)-N-(4-bromo-2-fluorobenzylidene)-2-methylpropane-2-sulfinamide
Ausbeute 103.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)[S@@](=O)/N=C/c1ccc(C(F)(F)F)cc1F
Reaction #85701
(R,E)-N-(2-fluoro-4-(trifluoromethyl)benzylidene)-2-methyl propane-2-sulfinamide
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)[S@@](=O)/N=C/c1cc(F)c(Br)cc1F
Reaction #85704
(R,E)-N-(4-bromo-2,5-difluorobenzylidene)-2-methylpropane-2-sulfinamide
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)[S@@](=O)/N=C/c1cccc(F)c1F
Reaction #85733
(R,E)-N-(2,3-difluorobenzylidene)-2-methylpropane-2-sulfinamide
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(F)(F)c1ccc(/C=N/[S@](=O)C(C)(C)C)c(F)c1
Reaction #85739
(R,E)-N-(4-(1,1-difluoroethyl)-2-fluorobenzylidene)-2-methylpropane-2-sulfinamide
Ausbeute 46.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)[S@@](=O)/N=C/c1ccc(OC(F)(F)F)cc1
Reaction #85745
(R,E)-2-methyl-N-(4-(trifluoromethoxy)benzylidene)propane-2-sulfinamide
Ausbeute 102.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1cccc(/C=N/[S@](=O)C(C)(C)C)c1
Reaction #92726
methyl 3-[(E)-{[(R)-tert-butylsulfinyl]imino}methyl]benzoate
Ausbeute 14.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)S(=O)/N=C/c1cccc(F)c1Cl
Reaction #167716
N-[1-(2-Chloro-3-fluorophenyl)meth-(E)-ylidene]-2-methylpropane-2-sulfinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C/C(=N\S(=O)C(C)(C)C)c1cc(Br)cc([N+](=O)[O-])c1
Reaction #168739
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)[S@@](=O)/N=C\c1ccc(Br)cc1Cl
Reaction #306355
(R,Z)-N-(4-bromo-2-chlorobenzylidene)-2-methylpropane-2-sulfinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
C[C@@H](c1ccc(Br)cc1)N(CCC/C(=N\[S@](=O)C(C)(C)C)c1ccccc1)C(=O)OC(C)(C)C
Reaction #306793
tert-butyl (S)-1-(4-bromophenyl)ethyl((E)-4-((R)-tert-butylsulfinylimino)-4-phenylbutyl)carbamate
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
C/C(=N\S(=O)C(C)(C)C)c1cc(Br)cc([N+](=O)[O-])c1
Reaction #308891
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cc1cc([C@@H](C)N[S@](=O)C(C)(C)C)ccc1NS(C)(=O)=O
Reaction #317767
title compound
Ausbeute 45.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CCOC(=O)c1cc([C@@H](C)N[S@](=O)C(C)(C)C)ccc1NS(C)(=O)=O
Reaction #317772
title compound
Ausbeute 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC(C)(C)[S@@](=O)N=C(c1ccc(F)cc1)c1cc(F)cc(OC(F)(F)C(F)F)c1
Reaction #325908
(R)—N-((3-fluoro-5-(1,1,2,2-tetrafluoroethoxy)phenyl)(4-fluorophenyl)methylene)-2-methylpropane-2-sulfinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COc1cc(/C(Cc2ccccc2)=N/[S@](=O)C(C)(C)C)ccc1F
Reaction #325949
(R,E)-N-(1-(4-fluoro-3-methoxyphenyl)-2-phenylethylidene)-2-methylpropane-2-sulfinamide
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[S@@](=O)N=C(c1cc(F)cc(OC(F)(F)C(F)F)c1)c1ccc(F)c(O[Si](C)(C)C(C)(C)C)c1
Reaction #325996
(R)—N-((3-(tert-butyldimethylsilyloxy)-4-fluorophenyl)(3-fluoro-5-(1,1,2,2-tetrafluoroethoxy)phenyl)methylene)-2-methylpropane-2-sulfinamide
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Seite 1Weiter