,
pages 273-306
The Chemistry of 2-Aminocyclopentanecarboxylic Acid
Publication type: Book Chapter
Publication date: 2000-01-01
SJR: —
CiteScore: 4.2
Impact factor: —
ISSN: 15725995
Abstract
The syntheses, transformations and some of the biological features of 2-aminocyclopentanecarboxylic acid are reviewed. The (1S,2R) enantiomer (cispentacin) was recently isolated from different natural sources. cis-2-Aminocyclopentacecarboxylic acid is also a component of the antibiotic amipurimycin. The paper discusses the syntheses of the racemic compounds, resolutions of the racemates and enetioselective syntheses of the title compounds. The transformations to heterocyclic compounds, applications in peptide syntheses, and biological effects are reviewed.
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15
Total citations:
15
Citations from 2024:
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TY - GENERIC
DO - 10.1016/S1572-5995(00)80028-9
UR - https://doi.org/10.1016/S1572-5995(00)80028-9
TI - The Chemistry of 2-Aminocyclopentanecarboxylic Acid
T2 - Studies in Natural Products Chemistry
AU - Fülöp, F.
PY - 2000
DA - 2000/01/01
PB - Elsevier
SP - 273-306
SN - 1572-5995
ER -
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@incollection{2000_Fülöp,
author = {F. Fülöp},
title = {The Chemistry of 2-Aminocyclopentanecarboxylic Acid},
publisher = {Elsevier},
year = {2000},
pages = {273--306},
month = {jan}
}