Issue 14, 1990

The total synthesis of (+)-norpatchoulenol: trapping of a non-enolizable 1,3-diketone intermediate with a Wittig reagent

Abstract

A short total synthesis of (+)-norpatchoulenol (1) has been accomplished from (+)icamphor-10-sulphonic acid (2) involving, as a key step, the trapping of a non-enolizable 1,3-diketone intermediate with a Wittig reagent.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 997-999

The total synthesis of (+)-norpatchoulenol: trapping of a non-enolizable 1,3-diketone intermediate with a Wittig reagent

H. Liu and M. Ralitsch, J. Chem. Soc., Chem. Commun., 1990, 997 DOI: 10.1039/C39900000997

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