21 件の反応に参加

34733

CCCCCCCCCCCCOCC(C)(O)CCNCCO
Reaction #1201
title compound
収率 30.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C[C@H](N)C(=O)O.N[C@@H](CO)C(=O)O
Reaction #4512
Alanine Serine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
N[C@@H](CO)C(=O)O.N[C@@H](Cc1ccccc1)C(=O)O
Reaction #4513
Phenylalanine Serine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C(O)CNC(=O)c1ccc(F)cc1
Reaction #4800
solid
収率 78.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COC(=O)N[C@@H](CO)C(C)C
Reaction #5035
N-Methyloxycarbonyl-D-valinol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(O)CNC(=O)C(F)(F)F
Reaction #11998
amide
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc2c(NCC(=O)O)cc(=O)oc2c1OC1CCCC1
Reaction #48913
2-(8-(cyclopentyloxy)-7-methoxy-2-oxo-2H-chromen-4-ylamino)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)Cn1cccc1
Reaction #54858
title compound
収率 33.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CSC(=S)NCC(=O)O
Reaction #55403
methyl carboxymethyldithiocarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=C(O)CN=CCc1ccc(O)cc1O
Reaction #61305
N-[(2,4-Dihydroxyphenyl)ethylidene]glycine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C=CCOC(=O)NCC(=O)O
Reaction #62557
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
C/C=C(/C=C/C(=O)NCC(=O)O)CC
Reaction #63849
N-[(E,E)-4-ethyl-2,4-hexadienoyl]glycine
収率 43.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCCCCCCCCCCC(=O)NCC(=O)O
Reaction #64593
N-n-dodecanoylglycine
収率 84.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCCCCCCCCCCNCC(=O)O
Reaction #64594
N-n-dodecylglycine
収率 26.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C(O)CNC(=O)c1ccccc1Cl
Reaction #72708
2-(2-chlorobenzamido)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)CNC(=O)c1ccccc1Cl
Reaction #72716
(2-Chloro-benzoylamino)-acetic acid
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
Reaction #76420
glucose
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=c1[nH]c2ccccc2[nH]c1=O
Reaction #81973
1,4-dihydro-2,3-quinoxalinedione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(O)CNc1cc(Br)c(Cl)cc1[N+](=O)[O-]
Reaction #82091
N-(5-Bromo-4-chloro-2-nitrophenyl)glycine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
—
Reaction #82102
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
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