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A synthesis of alpha,alpha-disubstituted aryl-beta-ketoesters

Stefaniak, M.H., Tinardon, F., Wallis, John D. (1997) A synthesis of alpha,alpha-disubstituted aryl-beta-ketoesters. Synlett, (6). pp. 677-678. ISSN 0936-5214. (doi:10.1055/s-1997-3249) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:17973)

The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided.
Official URL:
http://dx.doi.org/10.1055/s-1997-3249

Abstract

A generally applicable synthesis of alpha,alpha-disubstituted beta-ketoesters involving reaction of a substituted benzoyl chloride with methyl trimethylsilyl ketene acetal is described. Addition of boron trifluoride etherate is essential when the benzoyl chloride is nor substituted with a strongly electron withdrawing residue. The majority of experiments were conducted with the dimethylketene acetal but the process is equally applicable to the cyclohexaneketene acetal 5.

Item Type: Article
DOI/Identification number: 10.1055/s-1997-3249
Subjects: Q Science > QD Chemistry
Divisions: Divisions > Division of Natural Sciences > Physics and Astronomy
Depositing User: T.J. Sango
Date Deposited: 12 May 2009 09:03 UTC
Last Modified: 05 Nov 2024 09:53 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/17973 (The current URI for this page, for reference purposes)

University of Kent Author Information

Wallis, John D..

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