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Letter

Direct and Efficient One-Pot Preparation of Ketones from Aldehydes Using N-tert-Butylphenylsulfinimidoyl Chloride

Supporting Info

James J. Crawford,^† Kenneth W. Henderson,^‡ and William J. Kerr*^†

Department of Pure and Applied Chemistry, WestCHEM, University of Strathclyde, 295 Cathedral Street, Glasgow, Scotland, U.K. G1 1XL, and Department of Chemistry and Biochemistry, University of Notre Dame, 251 Nieuwland Science Hall, Notre Dame, Indiana 46556-5670

Org. Lett., 2006, 8 (22), pp 5073–5076

DOI: 10.1021/ol061903l

Publication Date (Web): October 5, 2006

†

Department of Pure and Applied Chemistry, WestCHEM, University of Strathclyde.

‡

Department of Chemistry and Biochemistry, University of Notre Dame.

In papers with more than one author, the asterisk indicates the name of the author to whom inquiries about the paper should be addressed.

, w.kerr@strath.ac.uk

Abstract

A general, one-pot process has been established to prepare ketones from aldehydes using N-tert-butylphenylsulfinimidoyl chloride. By employing the developed protocol, a range of unsymmetrical ketones has been prepared in good yields from aldehydes in one simple synthetic operation.

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Published In Issue October 26, 2006
Received August 1, 2006

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Letter

Direct and Efficient One-Pot Preparation of Ketones from Aldehydes Using N-tert-Butylphenylsulfinimidoyl Chloride

Abstract

Tools

SciFinder Links

History

Recommend & Share

Related Content

Iron-Catalyzed 1,4-Addition of α-Olefins to Dienes

Total Synthesis of (−)-Penifulvin A, an Insecticide with a Dioxafenestrane Skeleton

Enantiospecific Total Synthesis of the Hapalindoles, Fischerindoles, and Welwitindolinones via a Redox Economic Approach

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