Issue 18, 1988

Total synthesis of the ent-clerodane diterpenoids (±)-isolinaridiol and (±)-isolinaridiol diacetate

Abstract

A previously described mixture of bicyclo[4.4.0]decanecarbonitriles [(4) and (5)] was converted, via a nine-step sequence of reactions, into (±)-isolinaridiol (3), which was readily transformed into the corresponding diacetate (2).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 1245-1247

Total synthesis of the ent-clerodane diterpenoids (±)-isolinaridiol and (±)-isolinaridiol diacetate

E. Piers and J. S. M. Wai, J. Chem. Soc., Chem. Commun., 1988, 1245 DOI: 10.1039/C39880001245

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