D-serine

COC(=O)[C@H](N)CO.Cl
Reaction #90850
D-serine methyl ester hydrochloride
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)[C@@H](CO)NCc1ccccc1
Reaction #440434
desired compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
NC(CO)C(=O)NCc1ccccc1
Reaction #454206
N-Benzyl-2-aminohydracrylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
O=C(O)[C@@H](CO)NC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #476560
titled product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
O=C(O)[C@@H](CO)NC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #476561
titled product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
O=C(O)[C@@H](CO)NC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #476562
titled product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
O=C(O)[C@@H](CO)NC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #507288
titled product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
O=C(O)[C@@H](CO)NC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #507289
titled product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
O=C(O)[C@@H](CO)NC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #507290
titled product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
COC(=O)[C@H](N)CO.Cl
Reaction #538958
(R)-methyl 2-amino-3-hydroxypropanoate hydrochloride salt
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
Cc1c(N[C@H](CO)C(=O)O)ccc(C#N)c1Cl
Reaction #557945
final product
Ausbeute 29.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CC(C)(C)C(=O)OCCOC(=O)N[C@H](CO)C(=O)O
Reaction #579243
title compound ( 24 )
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
Cc1ccccc1C(=O)OCCOC(=O)N[C@H](CO)C(=O)O
Reaction #579244
title compound ( 25 )
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
CC(C)CC(=O)OCCOC(=O)N[C@H](CO)C(=O)O
Reaction #579245
title compound ( 26 )
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
O=C(N[C@H](CO)C(=O)O)OCCOC(=O)C1CCCCC1
Reaction #579246
title compound ( 27 )
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
O=C(N[C@H](CO)C(=O)O)OCCOC(=O)c1ccccc1
Reaction #579247
title compound ( 28 )
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
CC(C)C(=O)OCCOC(=O)N[C@H](CO)C(=O)O
Reaction #579248
title compound ( 29 )
Ausbeute 40.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
CCCC(=O)OCCOC(=O)N[C@H](CO)C(=O)O
Reaction #579249
title compound ( 30 )
Ausbeute 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
CCCCC(=O)OCCOC(=O)N[C@H](CO)C(=O)O
Reaction #579250
title compound ( 31 )
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
CC(C)C(=O)OCOC(=O)N[C@H](CO)C(=O)O
Reaction #579251
title compound ( 32 )
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
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