Issue 0, 1983
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

A new synthetic approach to quassinoids via an intramolecular Diels-Alder reaction: a stereoselective construction of the klaineanone ring system

Keiichiro Fukumoto,   Masatoshi Chihiro,   Masataka Ihara,   Tetsuji Kametani  and  Toshio Honda  

Abstract

Thermolysis of the benzocyclobutene derivative (25) prepared from norcamphor (6) gave stereoselectively the tetracyclic compound (27), which was converted into the D-deoxyquassinoid derivative (2) possessing the same ABCD-ring fusion as that of klaineanone (1).

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Article information

DOI
https://doi.org/10.1039/P19830002569
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1983, 2569-2576

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A new synthetic approach to quassinoids via an intramolecular Diels-Alder reaction: a stereoselective construction of the klaineanone ring system

K. Fukumoto, M. Chihiro, M. Ihara, T. Kametani and T. Honda, J. Chem. Soc., Perkin Trans. 1, 1983, 2569 DOI: 10.1039/P19830002569

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