An 35 Reaktionen beteiligt

444621

CC(C)(C)OC(=O)N[C@H](C=O)Cc1ccccc1
Reaction #67645
title compound
Ausbeute 100.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)N[C@H](C=O)Cc1ccccc1
Reaction #81113
title compound
Ausbeute 85.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(C)(C)OC(=O)N[C@H](C=O)Cc1ccccc1
Reaction #322693
title compound
Ausbeute 85.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CC(C)(C)OC(=O)N[C@H](C=O)Cc1ccccc1
Reaction #353027
title compound
Ausbeute 85.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CC(C)(C)OC(=O)N[C@H](C=O)Cc1ccccc1
Reaction #429808
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CC(C)(C)OC(=O)N[C@H](CNc1ccccc1)Cc1ccccc1
Reaction #429809
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CC(C)(C)OC(=O)N[C@H](C=O)Cc1ccccc1
Reaction #443954
title compound
Ausbeute 85.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
CC(C)(C)OC(=O)N[C@H](C=O)Cc1ccccc1
Reaction #490162
title compound
Ausbeute 100.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CC(C)(C)OC(=O)NC(Cc1ccccc1)C1C=C(c2ccccc2OCc2ccccc2)NC(N)=C1C(=O)OC(C)(C)C
Reaction #499464
tert-butyl 2-amino-6-[2-(benzyloxy)phenyl]-4-{1-[(tert-butoxycarbonyl)amino]-2-phenylethyl}-1,4-dihydro-3-pyridinecarboxylate
Ausbeute 16.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
CC(C)(C)OC(=O)N[C@H](C=O)Cc1ccccc1
Reaction #594936
title compound
Ausbeute 100.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CC(C)(C)OC(=O)N[C@H](C=O)Cc1ccccc1
Reaction #660190
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CC(C)(C)OC(=O)N[C@H](/C=C\Cc1ccccc1)Cc1ccccc1
Reaction #660191
tert-butyl-[(2S,3Z)-1,5-diphenylpent-3-en-2-yl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
C#C[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #686031
(S)-tert-butyl 1-phenylbut-3-yn-2-ylcarbamate
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CCOC(=O)C(F)(F)[C@H](O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #704819
ethyl 4(S)-[(tert-butoxycarbonyl)amino]-2,2-difluoro-3(R)-hydroxy-5-phenylpentanoate
Ausbeute 27.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
CC(C)(C)OC(=O)N[C@H](C=O)Cc1ccccc1
Reaction #730242
title compound
Ausbeute 111.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
C=C[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #730243
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CC(C)(C)OC(=O)N[C@H](C=O)Cc1ccccc1
Reaction #830103
title compound
Ausbeute 85.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
CC(C)(C)OC(=O)N[C@H](C=O)Cc1ccccc1
Reaction #832645
N-t-butoxycarbonyl-L-phenylalaninal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_07
CC(C)(C)OC(=O)N[C@H](C=O)Cc1ccccc1
Reaction #934809
crude desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_08
CC(C)(C)OC(=O)N[C@H](C=O)Cc1ccccc1
Reaction #976741
((S)-1-benzyl-2-oxo-ethyl)-carbamic acid tert-butyl ester
Ausbeute 106.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
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