Issue 17, 1999

New method for the synthesis of α-substituted tetrahydrofuran-2-methanols through diastereoselective addition of THF to aldehydes mediated by Et3B in the presence of air

Abstract

The tetrahydrofuranyl radical, generated from THF with Et3B in the presence of air, was found to react with aldehydes threo-selectively to afford α-substituted tetrahydrofuran-2-methanols, the common structural motifs of biologically active acetogenin polyketides, in moderate yields.

Article information

Article type
Paper

Chem. Commun., 1999, 1745-1746

New method for the synthesis of α-substituted tetrahydrofuran-2-methanols through diastereoselective addition of THF to aldehydes mediated by Et3B in the presence of air

T. Yoshimitsu, M. Tsunoda and H. Nagaoka, Chem. Commun., 1999, 1745 DOI: 10.1039/A904745J

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