Abstract
Syntheses of alkynyl- oxiranes and aziridines are rewieved. These compounds can serve as substrates in ring opening reactions with carbon nucleophiles to give allenyl- or homopropargylalcohols and amines.
Keywords: oxirane, aziridine, ring opening reaction, homopropargylalcohots, homopropargylamines
Current Organic Chemistry
Title: Alkynyl - Oxiranes and Aziridines: Synthesis and Ring Opening Reactions with Carbon Nucleophiles
Volume: 6 Issue: 6
Author(s): F. Chemla and F. Ferreira
Affiliation:
Keywords: oxirane, aziridine, ring opening reaction, homopropargylalcohots, homopropargylamines
Abstract: Syntheses of alkynyl- oxiranes and aziridines are rewieved. These compounds can serve as substrates in ring opening reactions with carbon nucleophiles to give allenyl- or homopropargylalcohols and amines.
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Cite this article as:
Chemla F. and Ferreira F., Alkynyl - Oxiranes and Aziridines: Synthesis and Ring Opening Reactions with Carbon Nucleophiles, Current Organic Chemistry 2002; 6 (6) . https://dx.doi.org/10.2174/1385272024604916
DOI https://dx.doi.org/10.2174/1385272024604916 |
Print ISSN 1385-2728 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5348 |
Call for Papers in Thematic Issues
Catalytic C-H bond activation as a tool for functionalization of heterocycles
The major topic is the functionalization of heterocycles through catalyzed C-H bond activation. The strategies based on C-H activation not only provide straightforward formation of C-C or C-X bonds but, more importantly, allow for the avoidance of pre-functionalization of one or two of the cross-coupling partners. The beneficial impact of ...read more
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