D-alanine

N[C@H](Cc1ccccc1)C(=O)O
Reaction #2053
D-phenylalanine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C[C@@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3cc4ccccc4o3)cc2)cc1)C(=O)O
Reaction #57775
N-({4′-[(1-benzofuran-2-ylcarbonyl)amino]-1,1′-biphenyl-4-yl}sulfonyl)-D-alanine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC(=O)N[C@H](C)C(=O)O
Reaction #68708
N-methoxycarbonyl-D-alanine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CNCC(=O)C(CCC[C@@H]1SC[C@@H]2NC(=O)N[C@@H]21)C(=O)O
Reaction #78018
N-methyl glycyl-biotin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@@H]21.O=C(O)CN1CCN(CC(=O)O)CCN(CC(=O)O)CCN(CC(=O)O)CC1
Reaction #83198
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CNCC(=O)C(CCC[C@@H]1SC[C@@H]2NC(=O)N[C@@H]21)C(=O)O
Reaction #83199
N-methyl glycyl-biotin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
C[C@@H](NC(=O)c1ncc2cc(Sc3ccccc3)ccc2c1O)C(=O)O
Reaction #337514
2-(R)-[(4-Hydroxy-7-phenylsulfanyl-isoquinoline-3-carbonyl)-amino]-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
C[C@@H](NC(=O)c1ncc2cc(Oc3ccccc3)ccc2c1O)C(=O)O
Reaction #337516
2-(R)-[(4-Hydroxy-7-phenoxy-isoquinoline-3-carbonyl)-amino]-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
O=C(O)CCCC[C@@H]1SC[C@@H]2NC(=O)N[C@@H]21.O=C(O)CN1CCN(CC(=O)O)CCN(CC(=O)O)CCN(CC(=O)O)CC1
Reaction #364799
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CNCC(=O)C(CCC[C@@H]1SC[C@@H]2NC(=O)N[C@@H]21)C(=O)O
Reaction #364800
N-methyl glycyl-biotin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
C[C@@H](NC(=O)OCc1ccccc1)C(=O)O
Reaction #458987
Nα -Benzyloxycarbonyl-D-alanine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_05
CNCC(=O)C(CCC[C@@H]1SC[C@@H]2NC(=O)N[C@@H]21)C(=O)O
Reaction #464193
N-methyl glycyl-biotin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
C[C@@H](NC(=O)c1nc(C#N)c2c(Oc3ccccc3)cccc2c1O)C(=O)O
Reaction #496472
title compound
Rendimiento 79.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
C[C@@H](NC(=O)OCc1ccccc1)C(=O)O
Reaction #524512
Nα-Benzyloxycarbonyl-D-alanine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_06
CCCOC(=O)Cc1c2n(c3ccccc13)C[C@H](N)CC2
Reaction #562670
crude title compound
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CCCOC(=O)Cc1c2n(c3ccccc13)C[C@H](N)CC2
Reaction #563409
crude title compound
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
C[C@@H](NC(=O)C(F)(F)F)C(=O)O
Reaction #582307
N-(trifluoroacetyl)-D-alanine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
C[C@@H](NC(=O)c1ncc2cc(Sc3ccccc3)ccc2c1O)C(=O)O
Reaction #610859
2-(R)-[(4-Hydroxy-7-phenylsulfanyl-isoquinoline-3-carbonyl)-amino]-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
C[C@@H](NC(=O)c1ncc2cc(Oc3ccccc3)ccc2c1O)C(=O)O
Reaction #610861
2-(R)-[(4-Hydroxy-7-phenoxy-isoquinoline-3-carbonyl)-amino]-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
—
Reaction #657025
material
Rendimiento 65.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_03
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