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Mendeleev Communications, 1992, Volume 2, Issue 1, Pages 20–21
DOI: https://doi.org/10.1070/MC1992v002n01ABEH000104 (Mi mendc5375) 		 
This article is cited in 2 scientific papers (total in 2 papers)

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

S. V. Verin, D. E. Tosunyan, E. V. Kuznetsov

Institute of Physical and Organic Chemistry, Southern Federal University, Rostov-on-Don, Russian Federation
Full-text PDF (234 kB) Citations (2)
DOI: https://doi.org/10.1070/MC1992v002n01ABEH000104
Abstract: 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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Document Type: Article
Language: English


Citation: S. V. Verin, D. E. Tosunyan, E. V. Kuznetsov, “An Efficient Access to α-Tetralones and their Derivatives via O-Quinodimethanes Generated by Isochromene Ring Cleavage”, Mendeleev Commun., 2:1 (1992), 20–21
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    • This publication is cited in the following 2 articles:
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