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

Chemo-Pharmaceutical Sciences

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

22 Citations (Scopus)

Abstract

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.

Original language	English
Pages (from-to)	1999-2006
Number of pages	8
Journal	Tetrahedron
Volume	56
Issue number	14
DOIs	https://doi.org/10.1016/S0040-4020(00)00089-2
Publication status	Published - Mar 31 2000

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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AU - Takahashi, Akira

AU - Aso, Mariko

AU - Tanaka, Masakazu

AU - Suemune, Hiroshi

PY - 2000/3/31

Y1 - 2000/3/31

N2 - 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.

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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JO - Tetrahedron

JF - Tetrahedron

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ER -

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

Abstract

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