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

研究成果: ジャーナルへの寄稿記事

19 引用 (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.

元の言語英語
ページ(範囲)1999-2006
ページ数8
ジャーナルTetrahedron
56
発行部数14
DOI
出版物ステータス出版済み - 3 31 2000

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

これを引用

Synthesis of optically active 9-oxabicyclo[3.3.1]nona-2,6-diene as a cycloocta-1,5-diene equivalent and the corresponding tetrol. / Takahashi, Akira; Aso, Mariko; Tanaka, Masakazu; Suemune, Hiroshi.

:: Tetrahedron, 巻 56, 番号 14, 31.03.2000, p. 1999-2006.

研究成果: ジャーナルへの寄稿記事

Takahashi, Akira ; Aso, Mariko ; Tanaka, Masakazu ; Suemune, Hiroshi. / Synthesis of optically active 9-oxabicyclo[3.3.1]nona-2,6-diene as a cycloocta-1,5-diene equivalent and the corresponding tetrol. :: Tetrahedron. 2000 ; 巻 56, 番号 14. pp. 1999-2006.
@article{f7eff4d2b9f44055b50bb28047220138,
title = "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 = "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.",
author = "Akira Takahashi and Mariko Aso and Masakazu Tanaka and Hiroshi Suemune",
year = "2000",
month = "3",
day = "31",
doi = "10.1016/S0040-4020(00)00089-2",
language = "English",
volume = "56",
pages = "1999--2006",
journal = "Tetrahedron",
issn = "0040-4020",
publisher = "Elsevier Limited",
number = "14",

}

TY - JOUR

T1 - Synthesis of optically active 9-oxabicyclo[3.3.1]nona-2,6-diene as a cycloocta-1,5-diene equivalent and the corresponding tetrol

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.

UR - http://www.scopus.com/inward/record.url?scp=0034737568&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0034737568&partnerID=8YFLogxK

U2 - 10.1016/S0040-4020(00)00089-2

DO - 10.1016/S0040-4020(00)00089-2

M3 - Article

AN - SCOPUS:0034737568

VL - 56

SP - 1999

EP - 2006

JO - Tetrahedron

JF - Tetrahedron

SN - 0040-4020

IS - 14

ER -