(S)-tert-butyl 1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate

COc1cccc(C(=O)[C@H](C)NC(=O)OC(C)(C)C)c1
Reaction #41289
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCc1ccc(C(=O)[C@H](C)NC(=O)OC(C)(C)C)cc1
Reaction #41293
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@H](NC(=O)OC(C)(C)C)C(=O)c1ccc2c(c1)OCCO2
Reaction #41299
(S)-tert-butyl 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-1-oxopropan-2-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@H](NC(=O)OC(C)(C)C)C(=O)c1ccc2ccccc2c1
Reaction #41302
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCc1cccc(C(=O)[C@H](C)NC(=O)OC(C)(C)C)c1
Reaction #41306
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cccc([C@@H](O)[C@H](C)NC(=O)OC(C)(C)C)c1
Reaction #41308
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@H](NC(=O)OC(C)(C)C)C(=O)c1ccc(C(F)(F)F)cc1
Reaction #41340
tert-Butyl {(1S)-1-methyl-2-oxo-2-[4-(trifluoromethyl)phenyl]ethyl}carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@H](NC(=O)OC(C)(C)C)C(=O)Cc1ccccc1
Reaction #41360
tert-Butyl N-[(2S)-3-oxo-4-phenyl-butan-2-yl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@H](NC(=O)OC(C)(C)C)C(=O)c1cnc2ccccc2c1
Reaction #41430
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@H](NC(=O)OC(C)(C)C)C(=O)c1ccccc1Cl
Reaction #41492
(S)-tert-butyl 1-(2-chlorophenyl)-1-oxopropan-2-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@@H](NC(=O)OC(C)(C)C)C(=O)c1ccc2c(c1)OCC2
Reaction #41502
subtitle compound
المردود 36.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(C(=O)[C@@H](C)NC(=O)OC(C)(C)C)ccc1SC
Reaction #41505
(R)-t-Butyl 1-(3-methoxy-4-(methylthio)phenyl)-1-oxopropan-2-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CON(C)C(=O)[C@H](C)NC(=O)OC(C)(C)C
Reaction #84300
desired product
المردود 53.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C[C@H](NC(=O)OC(C)(C)C)C(=O)c1ncc(Cl)cc1Cl
Reaction #84301
desired product
المردود 65.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CON(C)C(=O)[C@H](C)NC(=O)OC(C)(C)C
Reaction #508777
title compound
المردود 81.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
COC(=O)/C=C/[C@H](C)NC(=O)OC(C)(C)C
Reaction #508778
title compound
المردود 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CON(C)C(=O)[C@@H](C)NC(=O)OC(C)(C)C
Reaction #508780
title compound
المردود 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
C[C@H](NC(=O)OC(C)(C)C)C(=O)Cc1ccccc1
Reaction #560623
(S)-tert-butyl 3-oxo-4-phenylbutan-2-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CC(=O)[C@H](C)NC(=O)OC(C)(C)C
Reaction #584749
title compound
المردود 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_09
CON(C)C(=O)[C@H](C)NC(=O)OC(C)(C)C
Reaction #802830
title compound
المردود 81.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
الصفحة 1التالي