Enantioselective synthesis of a Wieland-Miescher ketone bearing an angular hydroxymethyl group

Article abstract of DOI:10.1080/00397919608003699

The enantioselective synthesis of (R)-3,4,8,8a-tetrahydro-8a-allyl-1,6-(2H,7H)-naphthalenedione and the degradation of the angular allyl group to a hydroxymethyl group are reported.

Full text of DOI:10.1080/00397919608003699

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Synthetic Communications:
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Enantioselective Synthesis
of A Wieland-Miescher
Ketone Bearing an Angular
Hydroxymethyl Group
Roger Hanselmann a & Michael Benn a
a Department of Chemistry , University of
Calgary , Calgary, Alberta, T2N 1N4, Canada
Published online: 21 Aug 2006.
To cite this article: Roger Hanselmann & Michael Benn (1996) Enantioselective
Synthesis of A Wieland-Miescher Ketone Bearing an Angular Hydroxymethyl Group,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 26:5, 945-961, DOI: 10.1080/00397919608003699
To link to this article: http://dx.doi.org/10.1080/00397919608003699
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