Conversion of Campholene- to Necrodane-Type Monoterpenes. A Short Stereoselective Synthesis of (-)-(R,R)-β-Necrodol and its Three Stereoisomers

DOI: 10.1002/hlca.19890720534

Source and publish data:

Helvetica Chimica Acta p. 1158 - 1163 (1989)

Update date:2022-08-11

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Authors:

Schulte-Elte, Karl H.

Pamingle, Herve

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Article abstract of DOI:10.1002/hlca.19890720534

Application of a stereoselective Prins/retro-Prins rearrangement sequence from (-)-(R)-campholenyl acetate ((-)-4) opens a new access to the naturally occuring (-)-(R,R)-β-necrodol ((-)-1 and its three stereoisomers with high optical purity.

Full text of DOI:10.1002/hlca.19890720534

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