Synthesis of optically active 9-oxabicyclo[3.3.1]nona-2,6-diene as a cycloocta-1,5-diene equivalent and the corresponding tetrol

Akira Takahashi; Mariko Aso; Masakazu Tanaka; Hiroshi Suemune

doi:10.1016/S0040-4020(00)00089-2

Synthesis of optically active 9-oxabicyclo[3.3.1]nona-2,6-diene as a cycloocta-1,5-diene equivalent and the corresponding tetrol

Akira Takahashi, Mariko Aso, Masakazu Tanaka, Hiroshi Suemune

医薬化学

研究成果: ジャーナルへの寄稿 › 学術誌 › 査読

22 被引用数 (Scopus)

抄録

Highly enantio- and diastereo-selective synthesis of C₂-symmetric 9- oxabicyclo[3.3.1]nona-2,6-diene and the corresponding C₂-symmetric 2,3,6,7- tetrol has been achieved starting from optically active 5-cyclooctene-1,2- diol prepared by an enzymatic procedure. (C) 2000 Elsevier Science Ltd.

本文言語	英語
ページ（範囲）	1999-2006
ページ数	8
ジャーナル	Tetrahedron
巻	56
号	14
DOI	https://doi.org/10.1016/S0040-4020(00)00089-2
出版ステータス	出版済み - 3月 31 2000

!!!All Science Journal Classification (ASJC) codes

生化学
創薬
有機化学

文献へのアクセス

10.1016/S0040-4020(00)00089-2

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引用スタイル

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AU - Aso, Mariko

AU - Tanaka, Masakazu

AU - Suemune, Hiroshi

PY - 2000/3/31

Y1 - 2000/3/31

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AB - Highly enantio- and diastereo-selective synthesis of C2-symmetric 9- oxabicyclo[3.3.1]nona-2,6-diene and the corresponding C2-symmetric 2,3,6,7- tetrol has been achieved starting from optically active 5-cyclooctene-1,2- diol prepared by an enzymatic procedure. (C) 2000 Elsevier Science Ltd.

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