A Synthesis of Substituted 3,6-Dihydro-1H-benzo[c]oxocines via Claisen Rearrangement and Ring-closing Metathesis

descriptionPublicationkeyboard_double_arrow_right Article 01 Jan 2002 English Publisher:CLOCKSS ArchiveJournal:HETEROCYCLES, volume 57, page 2,021 (issn: 0385-5414,

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Authors: Eng-Chi Wang; Chin-Cheng Wang; Ming-Kun Hsu; Keng-Shiang Huang;

doi: 10.3987/com-02-9560

A Synthesis of Substituted 3,6-Dihydro-1H-benzo[c]oxocines via Claisen Rearrangement and Ring-closing Metathesis

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Abstract

Started from isovanillin, based on Claisen rearrangement and ring-closing metathesis (RCM) reaction, a series of substituted 3,6-dihydro-1H-benzo[c]oxocines were synthesized in moderate yields.

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Kaohsiung Medical University
Taiwan

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