Synthetic study toward myrocin analogues. Highly enantio- and diastereo-selective synthesis of a tetracyclic ring system

Satoshi Yamada, Shigeru Nagashima, Yumiko Takaoka, Satsuki Torihara, Masakazu Tanaka, Hiroshi Suemune, Mariko Aso

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Abstract

An intramolecular Diels-Alder reaction for the construction of a lactone ring fused-tricyclic ring system has been developed using propionate as the dienophile. As an application of this reaction, an enantio- and diastereo-selective synthesis of a tetracyclic ring system of a myrocin analogue has been studied.

Original languageEnglish
Pages (from-to)1269-1274
Number of pages6
JournalJournal of the Chemical Society - Perkin Transactions 1
Issue number7
DOIs
Publication statusPublished - Apr 7 1998

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All Science Journal Classification (ASJC) codes

  • Chemistry(all)

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