(4+3)Cycloaddition Reactions Cycloaddition of Metal Oxyallyl Cations Generated from alph,alpha'-Di- and alph,alpha'-Poly-Haloketones to 1,3-Dienes and Anthracenes

Authors: El-Wareth A.; Sarhan A.O.

Source: Current Organic Chemistry, Volume 5, Number 7, July 2001 , pp. 827-844(18)

Publisher: Bentham Science Publishers

Abstract:

The (4+3)cyclocoupling reaction of allyl cations to 1,3-dienes is an efficient and easy route for the stereoselective synthesis of seven-membered ring compounds. Annulations using these species have opened easy access to a wide range of organic frameworks that have been utilized in the synthesis of natural products, pharmacologically active compounds and key intermediates for various useful organic and alkaloid compounds.

Keywords: Cycloaddition Reactions; Cycloaddition; Metal Oxyallyl Cations; Poly-Haloketones; 1,3-Dienes; Anthracenes; Cyclopropanones; Acyclic Dienes

Language: English

Document Type: Review article

DOI: http://dx.doi.org/10.2174/1385272013375184

Publication date: 2001-07-01

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• In this Subject: Organic Chemistry
• By this author: El-Wareth A. ;  Sarhan A.O.

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