(R)-2-amino-2-phenylacetic acid

COC(=O)N[C@@H](C(=O)O)c1ccccc1
Reaction #84044
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid
Rendement 65.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(O)Cc1ccccc1
Reaction #94075
phenylacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
COC(=O)[C@@H](N)c1ccccc1.Cl
Reaction #409232
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CC(=O)OC1CCCCC1
Reaction #516773
cyclohexyl acetate
Rendement 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
COC(=O)N[C@@H](C(=O)O)c1ccccc1
Reaction #803710
compound 31
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CCOC(=O)N[C@@H](C(=O)O)c1ccccc1
Reaction #803713
(R)-2-(ethoxycarbonylamino)-2-phenylacetic acid
Rendement 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
O=C(O)[C@@H](c1ccccc1)N1CCCC1
Reaction #1010578
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
O=C(O)[C@@H](c1ccccc1)N1CCOCC1
Reaction #1010580
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CCOC(=O)[C@H](N)c1ccccc1.Cl
Reaction #1256189
D-Phg-OEt hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_09
O=C1CC(c2ccccc2)NC(=O)N1
Reaction #1332525
6-phenyldihydropyrimidine-2,4(1H,3H)-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_10
COC(=O)N[C@@H](C(=O)O)c1ccccc1
Reaction #1573593
(R)-2-(methoxycarbonylamino)-2-phenylacetic acid
Rendement 65.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
CC1=C(C(=O)O)N2C(=O)[C@@H](NC(=O)[C@H](N)C3=CCC=CC3)[C@H]2SC1
Reaction #1581872
cefradin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_06
N[C@@H](CO)c1ccccc1
Reaction #1689268
(R)-2-Amino-2-phenylethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_11
CC1=C(C(=O)O)N2C(=O)[C@@H](NC(=O)[C@H](N)C3=CCC=CC3)[C@H]2SC1
Reaction #1738110
cefradin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_05
N[C@@H](C(=O)O)C1CCCCC1
Reaction #1773090
D-cyclohexylglycine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_04
COC(=O)N[C@@H](C(=O)O)c1ccccc1
Reaction #1898863
compound 31
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
CCOC(=O)N[C@@H](C(=O)O)c1ccccc1
Reaction #1898866
(R)-2-(ethoxycarbonylamino)-2-phenylacetic acid
Rendement 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
O=CNC(C(=O)O)c1ccccc1
Reaction #2060255
α-(formylamino)benzeneacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_12
O=C1N=C(N[C@@H](C(=O)O)c2ccccc2)S/C1=C\c1ccc2ncccc2c1
Reaction #2140523
(R)-{4-oxo-5-[1-quinolin-6-yl-meth-(Z)-ylidene]-4,5-dihydro-thiazol-2-ylamino}-phenyl-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_02
O=C(O)Cc1ccccc1
Reaction #2145689
phenylacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_03
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