Issue 0, 1972

The stereochemistry of some reactions of the sesquiterpenoid trichodermol

Abstract

Epoxidation of trichodermol and some derivatives gave the 9β, 10β-epoxide although osmylation appeared to give the 9α, 10α-glycol. Reduction of trichodermone with sodium borohydride gave 4-epitrichodermol. Elimination of the 4-hydroxy-group with phosphorus pentachloride afforded the Δ3-olefin without rearrangement.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1972, 2283-2285

The stereochemistry of some reactions of the sesquiterpenoid trichodermol

P. M. Adams and J. R. Hanson, J. Chem. Soc., Perkin Trans. 1, 1972, 2283 DOI: 10.1039/P19720002283

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