Regioselective deoxygenation of the cyclic thionocarbonates of 2,3- dihydroxy esters with magnesium in methanol

Article abstract of DOI:10.1080/00397919908086456

Deoxygenation of the cyclic thionocarbonates of 2,3-dihydroxy esters was mediated with magnesium in methanol, which provided a facile method for the synthesis of α-hydroxy esters.

Full text of DOI:10.1080/00397919908086456

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Synthetic Communications: An
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Regioselective Deoxygenation of
the Cyclic Thionocarbonates of 2,3-
Dihydroxy Esters with Magnesium in
Methanol
Ho-Sik Rho a & Byoung-Seob Ko b
a Pharmaceutical & Health Science Research Institute,
Pacific Corporation , Yongin-Si, Kyounggi-do, 449-900, Korea
b Korea Institute of Oriental Medicine , Chongdam-dong,
Kangnam-ku, Seoul, 135-100, Korea
Published online: 25 Sep 2007.
To cite this article: Ho-Sik Rho & Byoung-Seob Ko (1999) Regioselective Deoxygenation of
the Cyclic Thionocarbonates of 2,3-Dihydroxy Esters with Magnesium in Methanol, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic Organic
Chemistry, 29:16, 2875-2880, DOI: 10.1080/00397919908086456
To link to this article: http://dx.doi.org/10.1080/00397919908086456
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