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100 Years of the Wolff Rearrangement

2002; Wiley; Volume: 2002; Issue: 14 Linguagem: Inglês

10.1002/1099-0690(200207)2002

1434-193X

Wolfgang Kirmse,

Cyclopropane Reaction Mechanisms

The conversion of α-diazo ketones into ketenes, and products derived therefrom, was discovered by Wolff in 1902. Major applications of the Wolff rearrangement, such as the Arndt−Eistert reaction (homologation of carboxylic acids) and the ring contraction of cyclic ketones, have been with us for some while. Nevertheless, substantial progress has been made recently. The reaction mechanism has been explored by means of matrix isolation, time-resolved spectroscopy, and computation. Full retention of configuration of the migrating group has been established by using enantioselective chromatography. The Arndt−Eistert reaction has witnessed a renaissance in the field of natural products, in particular β-amino acids and β-peptides. Ring-contracting Wolff rearrangements and ketene cycloadditions have been applied in syntheses of increasingly complex, biologically active target molecules. These accomplishments, as well as unsolved problems, are addressed in the present review. (© Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002)