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

Chemo-Pharmaceutical Sciences

Research output: Contribution to journal › Article › peer-review

13 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 language	English
Pages (from-to)	1269-1274
Number of pages	6
Journal	Journal of the Chemical Society - Perkin Transactions 1
Issue number	7
DOIs	https://doi.org/10.1039/a708497h
Publication status	Published - Apr 7 1998

All Science Journal Classification (ASJC) codes

Chemistry(all)

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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.",

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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

Abstract

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