Allylic mono- and di-hydroxylation of isolated double bonds with selenium dioxide–tert-butyl hydroperoxide. NMR characterization of long-chain enols, allylic and saturated 1,4-diols, and enones-Reference-Cited by-同舟云学术

Allylic mono- and di-hydroxylation of isolated double bonds with selenium dioxide–tert-butyl hydroperoxide. NMR characterization of long-chain enols, allylic and saturated 1,4-diols, and enones

Published:1994 Issue:7 Volume: Page:1661-1669
ISSN:0300-9580
Container-title:J. Chem. Soc., Perkin Trans. 2
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 2

Author:

Knothe Gerhard,Bagby Marvin O.,Weisleder David,Peterson Robert E.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1994/P2/P29940001661

Reference73 articles.

1. P. C. B. Page and T. J.McCarthy, Oxidation Adjacent to CC Bonds, in Comprehensive Organic Synthesis, eds. B. M. Trost and I. Fleming, Pergamon, Oxford, 1991, vol. 7, pp. 83–117.

2. Allylic oxidation of olefins by catalytic and stoichiometric selenium dioxide with tert-butyl hydroperoxide

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