Synthesis of optically active allylic alcohols

Article abstract of DOI:10.1080/00397919308009827

A practical and enantiospecific method for the synthesis of optically pure allylic alcohols [(R)- or (S)-1-alken-3-ols] is described. The key reaction is the reductive cleavage of the cyclic carbonates of 1-halo-2,3-alkanediols with zinc, magnesium, or samarium diiodide.

Full text of DOI:10.1080/00397919308009827

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Synthesis of Optically Active
Allylic Alcohols
a
a
a
Suk-Ku Kang , Sung-Gyu Kim , Dong-Gyu Cho
&
a
Jae-Ho Jeon
a
Department of Chemistry , Sung Kyun Kwan
University, Natural Science Campus , Suwon,
440-746, Korea
Published online: 27 Oct 2006.
To cite this article: Suk-Ku Kang , Sung-Gyu Kim , Dong-Gyu Cho & Jae-Ho Jeon
(
1993) Synthesis of Optically Active Allylic Alcohols, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 23:5,
81-684, DOI: 10.1080/00397919308009827
6
To link to this article: http://dx.doi.org/10.1080/00397919308009827
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