Issue 23, 1986

An enantiospecific synthesis of longiborneol and longifolene

Abstract

(+)-8-Bromocamphor (7) is readily converted into a chiral enol ether acetal (8) which undergoes TiCl4-promoted cyclization to provide a tricyclic intermediate that can serve as a synthetic precursor of longibornane and longifolane sesquiterpenoids.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 1691-1692

An enantiospecific synthesis of longiborneol and longifolene

D. L. Kuo and T. Money, J. Chem. Soc., Chem. Commun., 1986, 1691 DOI: 10.1039/C39860001691

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