Issue 69, 2014

A metal-free dyotropic-like rearrangement of 2-oxa allylic alcohols in the presence of organoboronic acids

Abstract

The first example of a dyotropic-like rearrangement of 2-oxa allylic alcohols in the presence of catalytic amounts of Selectfluor and DABCO was reported, which provides a facile access to organoboronates. This reaction represents an unprecedented dyotropic rearrangement consisting of cleavage of two vicinal bonds (one C–C bond and one C[double bond, length as m-dash]C bond).

Graphical abstract: A metal-free dyotropic-like rearrangement of 2-oxa allylic alcohols in the presence of organoboronic acids

Supplementary files

Article information

Article type
Communication
Submitted
07 May 2014
Accepted
03 Jul 2014
First published
08 Jul 2014

Chem. Commun., 2014,50, 9879-9882

Author version available

A metal-free dyotropic-like rearrangement of 2-oxa allylic alcohols in the presence of organoboronic acids

W. Ye, W. Li and J. Zhang, Chem. Commun., 2014, 50, 9879 DOI: 10.1039/C4CC03450C

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