An Efficient Access to α-Tetralones and their Derivatives via O-Quinodimethanes Generated by Isochromene Ring Cleavage

An Efficient Access to α-Tetralones and their Derivatives via O-Quinodimethanes Generated by Isochromene Ring Cleavage

The stereoselectivity of the formation of cis-3,4-dihydronaphthalenes from 1-styryl substituted isochromenes proves the intermediacy of O-quinodimethanes in this reaction.

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Veröffentlicht in:Mendeleev communications 1992, Vol.2 (1), p.20-21
Hauptverfasser: Verin, Sergei V., Tosunyan, Dmitrii E., Kuznetsov, Evgenli V.
Format: Artikel
Sprache:eng
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Zusammenfassung:The stereoselectivity of the formation of cis-3,4-dihydronaphthalenes from 1-styryl substituted isochromenes proves the intermediacy of O-quinodimethanes in this reaction.
ISSN:0959-9436
DOI:10.1070/MC1992v002n01ABEH000104