An improved procedure for the preparation of the O,2-dianion of allyl alcohol

Article abstract of DOI:10.1080/00397919708006818

An improved procedure for the preparation of the O,2-dianion of allyl alcohol is described. The use of the magnesium alkoxide of 2-bromopropen-1- ol instead of the known lithium salt, suppresses dehydrohalogenation upon treatment with tert-butyl lithium a

Full text of DOI:10.1080/00397919708006818

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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An Improved Procedure for the
Preparation of the O,2-Dianion
of Allyl Alcohol
Sayee G. Hegde a & David C. Myles a
a Department of Chemistry and Biochemistry , UCLA,
Los Angeles, CA, 90095-1569
Published online: 22 Aug 2006.
To cite this article: Sayee G. Hegde & David C. Myles (1997) An Improved Procedure
for the Preparation of the O,2-Dianion of Allyl Alcohol, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 27:12,
2111-2115, DOI: 10.1080/00397919708006818
To link to this article: http://dx.doi.org/10.1080/00397919708006818
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