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

Research output: Contribution to journalArticle

19 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 languageEnglish
Pages (from-to)1999-2006
Number of pages8
JournalTetrahedron
Volume56
Issue number14
DOIs
Publication statusPublished - Mar 31 2000

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

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.

In: Tetrahedron, Vol. 56, No. 14, 31.03.2000, p. 1999-2006.

Research output: Contribution to journalArticle

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. In: Tetrahedron. 2000 ; Vol. 56, No. 14. pp. 1999-2006.
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