2002Current Organic ChemistryRequires access

Alkynyl - Oxiranes and Aziridines: Synthesis and Ring Opening Reactions with Carbon Nucleophiles

Fabrice Chemla, Franck Ferreira

Open publisher page 55 citations

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

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What this paper is about

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

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Available 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

Key concepts: Aziridine, Chemistry, Nucleophile, Ring (chemistry), Carbon fibers, Organic chemistry, Combinatorial chemistry, Medicinal chemistry

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