d,l-norvaline

CCCC(C(=O)O)n1cccc1
Reaction #54592
2-(1-pyrryl)pentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC(C)C(NC(=O)OC(C)(C)C)C(=O)O
Reaction #183034
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCC(NC(=O)OCc1ccccc1)C(=O)O
Reaction #390580
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
—
Reaction #460043
white crystals
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_05
—
Reaction #460044
white crystals
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_05
CCCC(N)C(=O)OCC
Reaction #699572
2-aminopentanoic acid ethyl ester
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
CCCC(NC(=O)OCC)C(=O)O
Reaction #758247
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Cl
Reaction #782306
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Cl
Reaction #784059
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(C)CC(N)C(N)=O
Reaction #924993
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCCc1nc(C)c(C(C)=O)[nH]1
Reaction #1162465
5-acetyl-4-methyl-2-propylimidazole
المردود 55.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_07
CCCc1nc(C)c(C(C)=O)[nH]1
Reaction #1162466
5-acetyl-4-methyl-2-propylimidazole
المردود 43.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_07
C#CC(=O)c1[nH]c(CCC)nc1C
Reaction #1162471
4-methyl-5-propinoyl-2-propylimidazole
المردود 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_07
CCCC(N)C(=O)OC
Reaction #1238158
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CC[C@H]1OC(=O)C[C@@H](O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)[C@@H](O[C@H]3C[C@@](C)(O)[C@@H](O)[C@H](C)O3)[C@H](N(C)C)[C@H]2O)[C@@H](CC=O)C[C@@H](C)C(=O)/C=C/C(C)=C/[C@@H]1CO[C@@H]1O[C@H](C)[C@@H](O)[C@@H](OC)[C@H]1OC
Reaction #1482247
tylosin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_05
CC[C@H]1OC(=O)C[C@@H](O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)[C@@H](O[C@H]3C[C@@](C)(O)[C@@H](O)[C@H](C)O3)[C@H](N(C)C)[C@H]2O)[C@@H](CC=O)C[C@@H](C)C(=O)/C=C/C(C)=C/[C@@H]1CO[C@@H]1O[C@H](C)[C@@H](O)[C@@H](OC)[C@H]1OC
Reaction #1482248
tylosin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_05
CCCc1nc(C)c(C(C)=O)[nH]1
Reaction #1549398
5-acetyl-4-methyl-2-propylimidazole
المردود 55.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_07
CCCc1nc(C)c(C(C)=O)[nH]1
Reaction #1549399
5-acetyl-4-methyl-2-propylimidazole
المردود 43.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_07
C#CC(=O)c1[nH]c(CCC)nc1C
Reaction #1549404
4-methyl-5-propinoyl-2-propylimidazole
المردود 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_07
CCCC(Nc1nc2ccc(Cl)cc2cc1C(=O)O)C(=O)O
Reaction #2152774
title compound
المردود 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_10
الصفحة 1التالي