参与 175 个反应

4517

O=C(O)CCCNC(=O)c1ccccc1SSc1ccccc1C(=O)NCCCC(=O)O
Reaction #3357
title compound
收率 49.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCCNC(=O)OCc1ccccc1
Reaction #55626
N-carbobenzoxy-γ-aminobutyric acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=C(O)CCCNC(=O)c1ccccc1SSc1ccccc1C(=O)NCCCC(=O)O
Reaction #81951
title compound
收率 49.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(O)CCCNC(=O)OCc1ccc([N+](=O)[O-])cc1
Reaction #175725
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CCCNC(=O)OCc1ccccc1
Reaction #211331
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CCCNC(=O)c1ccccc1
Reaction #265524
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(O)CCCN1C(=O)c2ccc(C(=O)O)cc2C1=O
Reaction #274452
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC(=O)c1cc2c3c(cccc3c1)C(=O)N(CCCC(=O)O)C2=O
Reaction #276602
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NCCCC(O)(P(=O)(O)O)P(=O)(O)O
Reaction #340910
product
收率 43.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
—
Reaction #342203
powder
收率 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
Cl.NCCCC(=O)OCc1ccccc1
Reaction #347385
4-Aminobutanoic acid benzyl ester hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
Cl.NCCCC(=O)OC1CCCCC1
Reaction #347386
4-Aminobutanoic acid cyclohexyl ester hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
COC(=O)CCCNC(=O)OCc1ccccc1
Reaction #364107
methyl 4-(benzyloxycarbonylamino)butyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cc(Cl)cc(C(=NCCCC(=O)O)c2ccc(Cl)cc2)c1O
Reaction #367460
4-{[(5-Chloro-2-hydroxy-3-methylphenyl)-(4-chlorophenyl)-methylene]-amino}-butanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_05
COCCCOc1cc(CC(CC(NC(=O)OC(C)(C)C)C(O)CN2CCCC2=O)C(C)C)ccc1OC
Reaction #379149
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(O)CCCNC(=O)OCc1ccccc1
Reaction #391618
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(O)CCCN1C(=O)c2ccccc2C1=O
Reaction #393003
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1CC(C)CN(S(=O)(=O)c2ccc(Cl)c(C(=O)NCCCC(=O)O)c2)C1
Reaction #393544
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCCCNC(=O)CCCN
Reaction #402754
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)C(=O)NCCCC(=O)O
Reaction #413950
N-(2-methyl)propionyl-4-aminobutanoic acid
收率 43.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
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