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Superacidic cyclization of terpenoids

Pure and Applied Chemistry (1993) 65(6) 1329-1336
DOI: 10.1351/pac199365061329
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Abstract

A general highly efficient structure-selective and stereospecific method of superacidic cyclization of terpenoid alcohols and their acetates, acids, esters and also of homo- and bishomoterpenoid alcohols, acids and esters has been elaborated. The terminal terpenic epoxides do not cyclize, undergoing isomerization and opening of the oxirane cycle. © 1993 IUPAC

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APA

Vlad, P. F. (1993). Superacidic cyclization of terpenoids. Pure and Applied Chemistry, 65(6), 1329–1336. https://doi.org/10.1351/pac199365061329

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