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Issue 17, 1988
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A concise enantioselective route to (–)-kainic acid from (S)-2-(benzyloxymethyl)oxirane

Abstract

A concise enantioselective route to (–)-kainic acid (1) from (S)-2-(benzyloxymethyl)oxirane (2) has been established by enantio- and diastereo-selective intramolecular 1,3-dipolar cyclization.

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Article information


J. Chem. Soc., Chem. Commun., 1988, 1204-1206
Article type
Paper

A concise enantioselective route to (–)-kainic acid from (S)-2-(benzyloxymethyl)oxirane

S. Takano, Y. Iwabuchi and K. Ogasawara, J. Chem. Soc., Chem. Commun., 1988, 1204
DOI: 10.1039/C39880001204

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