L-valinol

CC(C)[C@@H](CO)NC(=O)[C@@H](CC(=O)N1CCOCC1)c1ccc(F)cc1
Reaction #43563
2-(S)-(4-Fluoro-phenyl)-N-(1-(S)-hydroxymethyl-2-methyl-propyl)-4-morpholin-4-yl-4-oxo-butyramide
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)[C@@H](CO)NC(=O)c1cc(F)c2[nH]nc(/C=C/c3cccnc3)c2c1
Reaction #62306
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)[C@@H](CO)NC(=O)OCc1ccccc1
Reaction #81391
N-benzyloxycarbonyl-valinol
Ausbeute 95.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(C)[C@@H](CO)NC(=O)C1(NC(=O)c2ccco2)CCCCC1
Reaction #161027
title compound
Ausbeute 74.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)[C@@H](CO)NC(=O)C1(NC(=O)OCc2ccco2)CCCCC1
Reaction #161063
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1ccc(C(=O)NC2(C(=O)N[C@H](CO)C(C)C)CCCCC2)cc1
Reaction #161064
title compound
Ausbeute 66.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)[C@@H](CO)NC(=O)C1(NC(=O)c2ccc[nH]2)CCCCC1
Reaction #161065
title compound
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N[C@H](CO)C(C)C)cn1
Reaction #170510
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)[C@@H](CO)NCCCS(=O)(=O)O
Reaction #326933
3-[(1S)-1-(hydroxymethyl)-2-methylpropyl]amino-1-propanesulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)[C@H]1COCC(=O)N1
Reaction #337028
(S)-5-isopropylmorpholin-3-one
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Cc1cc([N+](=O)[O-])ccc1N=C1N[C@@H](C(C)C)CS1
Reaction #363660
(45)-2-(2-methyl-4-nitrophenylimino)-4-isopropyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cc([N+](=O)[O-])ccc1N=C1N[C@@H](C(C)C)CS1
Reaction #363674
(4S)-2-(2-methyl-4-nitrophenylimino)-4-isopropyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CC(C)C1N[C@@H](C(C)C)CO1
Reaction #363871
(4S)-2,4diisopropyl-1,3-oxazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CC(C)[C@@H](CO)NC(=O)OCc1ccccc1
Reaction #413718
alcohol
Ausbeute 79.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
CC(C)[C@H]1COC(=O)N1
Reaction #414096
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N[C@H](CO)C(C)C)cn1
Reaction #419109
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N[C@H](CO)C(C)C)cn1
Reaction #419609
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)[C@H]1COC(=O)N1
Reaction #429176
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CC(C)C1COCC(=O)N1
Reaction #446530
5-(2-propyl)-3-morpholinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
CC(C)[C@@H](CO)NC(=O)OCc1ccccc1
Reaction #450919
N-benzyloxycarbonyl-valinol
Ausbeute 95.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
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