Issue 5, 1998
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Asymmetric synthesis of (2R,4R,5S)-tetrahydropseudodistomin and stereoisomers by cycloaddition of nitrone to vinylglycinol 1

Toshiko Kiguchi,   Miho Ikai,   Mitsuko Shirakawa,   Kuniko Fujimoto,   Ichiya Ninomiya  and  Takeaki Naito  

Abstract

Cycloaddition of the nitrone, derived from tetradecanal, to vinylglycinol provides an asymmetric synthesis of both (2R,4R,5S)-tetrahydropseudodistomin and all the stereoisomers of the racemic tetrahydropseudodistomins.

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Article information

DOI
https://doi.org/10.1039/A707797A
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1998, 893-900

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Asymmetric synthesis of (2R,4R,5S)-tetrahydropseudodistomin and stereoisomers by cycloaddition of nitrone to vinylglycinol 1

T. Kiguchi, M. Ikai, M. Shirakawa, K. Fujimoto, I. Ninomiya and T. Naito, J. Chem. Soc., Perkin Trans. 1, 1998, 893 DOI: 10.1039/A707797A

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