Issue 2, 2008

The [1, 3] O-to-C rearrangement: opportunities for stereoselective synthesis

Abstract

The relay of stereochemistry of a breaking C–O bond into a forming C–C bond is well-known in the context of [3, 3] sigmatropic shifts; however, this useful strategy is less well-known in other types of molecular rearrangements. Though the first successful example of a [1, 3] O-to-C rearrangement was reported more than 100 years ago, this class of reactions has received less attention than its [3, 3] counterpart. This perspective analyzes the various methods used for the activation and [1, 3] rearrangement of vinyl ethers with an emphasis on mechanism and applications to stereoselective synthesis. We also highlight our own contributions to this area.

Graphical abstract: The [1, 3] O-to-C rearrangement: opportunities for stereoselective synthesis

Article information

Article type
Perspective
Submitted
27 Sep 2007
First published
04 Dec 2007

Org. Biomol. Chem., 2008,6, 240-254

The [1, 3] O-to-C rearrangement: opportunities for stereoselective synthesis

C. G. Nasveschuk and T. Rovis, Org. Biomol. Chem., 2008, 6, 240 DOI: 10.1039/B714881J

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