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

doi:10.1039/a708497h

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

医薬化学

研究成果: ジャーナルへの寄稿 › 学術誌 › 査読

4 被引用数 (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.

本文言語	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
号	7
DOI	https://doi.org/10.1039/a708497h
出版ステータス	出版済み - 4月 7 1998

!!!All Science Journal Classification (ASJC) codes

化学 (全般)

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10.1039/a708497h

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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.",

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

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T1 - Synthetic study toward myrocin analogues. Highly enantio- and diastereo-selective synthesis of a tetracyclic ring system

AU - Yamada, Satoshi

AU - Nagashima, Shigeru

AU - Takaoka, Yumiko

AU - Torihara, Satsuki

AU - Tanaka, Masakazu

AU - Suemune, Hiroshi

AU - Aso, Mariko

PY - 1998/4/7

Y1 - 1998/4/7

N2 - 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.

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

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!!!All Science Journal Classification (ASJC) codes

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