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Issue 10, 1996
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Synthesis of (–)-furodysinin from (+)-limonene


Furodysinin is synthesised by elaboration of (1R, 2R)-(+)-limonene oxide; key reactions include a tandem Claisen rearrangement–ene reaction and trapping of a conjugate adduct of an enone providing a bicyclic precursor of the sesquitepene.

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Chem. Commun., 1996, 1147-1147
Article type

Synthesis of (–)-furodysinin from (+)-limonene

T. Ho and R. Chein, Chem. Commun., 1996, 1147
DOI: 10.1039/CC9960001147

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