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Issue 17, 1988
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A new route to substituted 3-methoxycarbonyldihydropyrans; enantioselective synthesis of (–)-methyl elenolate

Abstract

A stereoselective chiral synthesis of (–)-methyl elenolate has been achieved by employing a newly developed method for the construction of substituted 3-methoxycarbonyldihydropyrans based on a radical cyclisation reaction.

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Article information


J. Chem. Soc., Chem. Commun., 1988, 1202-1204
Article type
Paper

A new route to substituted 3-methoxycarbonyldihydropyrans; enantioselective synthesis of (–)-methyl elenolate

S. Hatakeyama, N. Ochi, H. Numata and S. Takano, J. Chem. Soc., Chem. Commun., 1988, 1202 DOI: 10.1039/C39880001202

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