R-3-Methyl-γ-butyrolactone as a Template for the Synthesis of (+)-Invictolide

DOI: 10.1016/S0040-4039(00)84224-0

Source and publish data:

Tetrahedron Letters p. 1229 - 1232 (1986)

Update date:2022-08-04

Topics:

Authors:

Ziegler, Frederick E.

Wester, Ronald T.

Stirchak, Eugene P.

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Article abstract of DOI:10.1016/S0040-4039(00)84224-0

The dextrorotatory antipode of the pheromone invictolide has been synthesized from R-3-methyl-γ-butyrolactone, which is employed as a stereochemical template for the addition of propionate units via a Claisen rearrangement and a palladium-catalyzed alkyla

Full text of DOI:10.1016/S0040-4039(00)84224-0

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