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DOI: 10.1039/A707797A (Paper) Reference Section for: J. Chem. Soc., Perkin Trans. 1, 1998, 893-900

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

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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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