Issue 24, 1997

Lewis acid mediated [3 + 2] cycloaddition of allylgermane: stereoselective synthesis of germyl substituted tetrahydrofurans

Abstract

Tin(IV) chloride mediated [3 + 2] cycloaddition of allylgermanes to α-dicarbonyl compounds proceeds highly stereoselectively to give tetrahydrofurans in good yields.

Article information

Article type
Paper

Chem. Commun., 1997, 2357-2358

Lewis acid mediated [3 + 2] cycloaddition of allylgermane: stereoselective synthesis of germyl substituted tetrahydrofurans

T. Akiyama, Chem. Commun., 1997, 2357 DOI: 10.1039/A706497G

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