New construction of the bicyclo[3.3.1]nonane system via Lewis acid promoted regioselective ring-opening reaction of the tricyclo[4.4.0.05,7]dec-2-ene derivative

Masahito Abe, Masahisa Nakada

Research output: Contribution to journalArticlepeer-review

26 Citations (Scopus)

Abstract

A new access to the bicyclo[3.3.1]nonane system, which is a common structure in a number of polyisoprenylated phloroglucinol derivatives (phloroglucins), has been developed via the Lewis acid promoted regioselective ring-opening reaction of the cyclopropane, a tricyclo[4.4.0.05,7]dec-2-ene derivative.

Original languageEnglish
Pages (from-to)6347-6351
Number of pages5
JournalTetrahedron Letters
Volume47
Issue number36
DOIs
Publication statusPublished - 2006 Sep 4

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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