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Transition Metal-catalyzed Synthesis and Reactivity of N-alkenyl Aziridines

Overview
Journal Org Lett
Specialties Biochemistry
Chemistry
Date 2005 Mar 12
PMID 15760164
Citations 5
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Abstract

[reaction: see text] Straightforward methods for palladium-catalyzed alkenylation of aziridines with alkenyl halides and copper-catalyzed alkenylation of aziridines with alkenyl boronic acids have been developed. This methodology offers attractive alternatives to the known methods requiring activated alkenyl halides and acetylenes. A wide variety of N-alkenyl aziridines containing substituents other than electron-withdrawing substituents such as cyano groups and sulfones have been synthesized in good yields. Furthermore, these N-alkenyl aziridines exhibit quite a different reactivity from conventional enamines, as demonstrated by their reactivity.

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