Issue 14, 1983

Enantio- and diastereo-selective reaction of but-2-enylstannane with glyoxylate esters and its application to a short synthesis of verrucarinolactone

Abstract

The erythro-3-alkyl-2-hydroxypropionate unit in (4) is predominantly obtained via the reaction of but-2-enylstannane (2a) with glyoxylate esters (3) while the threo-isomer (5) is preferentially produced via 9-but-2-enyl-9-borabicyclo[3.3.1] nonane (2b); the former reaction has been applied to the enantioselective synthesis of verrucarinolactone (6).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 774-775

Enantio- and diastereo-selective reaction of but-2-enylstannane with glyoxylate esters and its application to a short synthesis of verrucarinolactone

Y. Yamamato, N. Maeda and K. Maruyama, J. Chem. Soc., Chem. Commun., 1983, 774 DOI: 10.1039/C39830000774

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