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

研究成果: ジャーナルへの寄稿記事

11 引用 (Scopus)

抄録

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.

元の言語英語
ページ(範囲)1269-1274
ページ数6
ジャーナルJournal of the Chemical Society - Perkin Transactions 1
発行部数7
DOI
出版物ステータス出版済み - 4 7 1998

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Propionates
Lactones

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

これを引用

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.

:: Journal of the Chemical Society - Perkin Transactions 1, 番号 7, 07.04.1998, p. 1269-1274.

研究成果: ジャーナルへの寄稿記事

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. :: Journal of the Chemical Society - Perkin Transactions 1. 1998 ; 番号 7. pp. 1269-1274.
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