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DOI: 10.1039/A708497H (Paper) Reference Section for: J. Chem. Soc., Perkin Trans. 1, 1998, 1269-1274

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

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

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.

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