A NOVEL METHOD FOR THE TERPENE SYNTHESIS BY THE RING-OPENING REACTION OF β-METHYL-β-PROPIOLACTONE

DOI: 10.1016/0040-4039(80)80126-2

Source and publish data:

Tetrahedron Letters p. 2553 - 2554 (1980)

Update date:2022-08-18

Topics:

Authors:

Fujisawa, Tamotsu

Sato, Toshio

Kawara, Tatsuo

Noda, Atsunari

Obinata,Toshiyuki

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Article abstract of DOI:10.1016/0040-4039(80)80126-2

A new route for the terpene synthesis is investigated, which undergoes via terpene carboxylic acids as key intermediates obtained by the regiospecific ring opening of β-methyl-β-propiolactone with cuprate or with a Grignard reagent in the presence of a copper catalyst.

Full text of DOI:10.1016/0040-4039(80)80126-2

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