Catalytic Conversion of Furans and Pyrroles to Natural Products and Analogues Utilizing Donor-Acceptor Substituted Cyclopropanes as Key Intermediates

Reiser, Oliver (2016) Catalytic Conversion of Furans and Pyrroles to Natural Products and Analogues Utilizing Donor-Acceptor Substituted Cyclopropanes as Key Intermediates. ISRAEL JOURNAL OF CHEMISTRY, 56 (6-7). pp. 531-539. ISSN 0021-2148, 1869-5868

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Abstract

This review is an account of our work on developing stereoselective cyclopropanations of furans and pyrroles as a facile entry into donor-acceptor substituted cyclopropanes. The application of these building blocks for the synthesis of paraconic acids, sesquiterpene lactones, pyrrolidinones, and conformationally restricted -amino acids is discussed.

Item Type: Article
Uncontrolled Keywords: BETA-AMINOCYCLOPROPANECARBOXYLIC ACIDS; SHORT ALPHA/BETA-PEPTIDES; ENANTIOSELECTIVE SYNTHESIS; STEREOSELECTIVE-SYNTHESIS; ASYMMETRIC CYCLOPROPANATION; LIGNOCELLULOSIC BIOMASS; HELICAL CONFORMATIONS; STRUCTURAL-PROPERTIES; ORGANIC-SYNTHESIS; CARBOXYLIC-ACIDS; donor-acceptor systems; furans; lactones; pyrroles; pyrrolidinones; gamma-butyrolactons
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Oliver Reiser
Depositing User: Petra Gürster
Date Deposited: 02 Sep 2020 05:49
Last Modified: 02 Sep 2020 05:49
URI: https://pred.uni-regensburg.de/id/eprint/2816

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