Substructure Search

773827

COC(=O)[C@@H]1C=C[C@H](NC(C)=O)C1
Reaction #56068
methyl(+)-cis-4-acetamidocyclopent-2-ene carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1(N)C=CC(C(=O)O)C1
Reaction #456687
product
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C=C[C@H](NC(C)=O)C1
Reaction #938419
methyl-cis-4-acetamidocyclopent-2-ene carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1(N)C=CC(C(=O)O)C1
Reaction #1156983
product
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1(N)C=CC(C(=O)O)C1
Reaction #1361614
product
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1(N)C=CC(C(=O)O)C1
Reaction #1472766
product
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C=C[C@H](NC(C)=O)C1
Reaction #1477531
methyl (+)-cis-4-acetamidocyclopent-2-ene carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C=C[C@H](N)C1.Cl
Reaction #1514508
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C=C[C@H](NC(c2ccccc2)(c2ccccc2)c2ccccc2)C1
Reaction #1514509
title compound
Yield 105.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C=C[C@@H](N)C1.Cl
Reaction #1834323
(1R,4S)-methyl 4-aminocyclopent-2-enecarboxylate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C=C[C@H](N)C1.Cl
Reaction #1910523
cis-4-amino-2-cyclopentene-1-carboxylic acid methyl ester hydrochloride
Yield 94.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C=C[C@H](N)C1.Cl
Reaction #1910524
cis-4-amino-2-cyclopentene-1-carboxylic acid methyl ester hydrochloride
Yield 78.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H]1C=C[C@H](N)C1.Cl
Reaction #1971154
(−)-ethyl cis-4-amino-2-cyclopentene-1-carboxylate hydrochloride
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C=C[C@H](NC(C)=O)C1
Reaction #2374202
methyl (±)-cis-4-acetamidocyclopent-2-ene carboxylate
DOI: 10.6084/m9.figshare.5104873.v1