ZUR REGIOSELEKTIVITAET BEIM ALDOL-RINGSCHLUSS

DOI: 10.1016/0040-4039(81)80117-7

Source and publish data:

Tetrahedron Letters p. 429 - 432 (1981)

Update date:2022-09-26

Topics:

Authors:

Kreiser, Wolfgang

Below, Peter

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Article abstract of DOI:10.1016/0040-4039(81)80117-7

According to the proper choice of reaction conditions, a regioselective ring closure of the 1,5-diketones I is achieved, either to II or III.This directed aldolisation was successfully applied to a short synthesis of the monoterpenoid piperitone.

Full text of DOI:10.1016/0040-4039(81)80117-7

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