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

Research output: Contribution to journalArticle

11 Citations (Scopus)

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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Propionates
Lactones

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

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Synthetic study toward myrocin analogues. Highly enantio- and diastereo-selective synthesis of a tetracyclic ring system. / Yamada, Satoshi; Nagashima, Shigeru; Takaoka, Yumiko; Torihara, Satsuki; Tanaka, Masakazu; Suemune, Hiroshi; Aso, Mariko.

In: Journal of the Chemical Society - Perkin Transactions 1, No. 7, 07.04.1998, p. 1269-1274.

Research output: Contribution to journalArticle

Yamada, Satoshi ; Nagashima, Shigeru ; Takaoka, Yumiko ; Torihara, Satsuki ; Tanaka, Masakazu ; Suemune, Hiroshi ; Aso, Mariko. / Synthetic study toward myrocin analogues. Highly enantio- and diastereo-selective synthesis of a tetracyclic ring system. In: Journal of the Chemical Society - Perkin Transactions 1. 1998 ; No. 7. pp. 1269-1274.
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