A synthetic method for preparing 3,3-dialkyl-1,2,3,8-tetrahydroazulen-1- one

Mitsunori Oda, Takanori Kajioka, Kazuya Ikeshima, Ryuta Miyatake, Shigeyasu Kuroda*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

The trimethylsilyl enol ether of 1-acetylcyclohepta-1,3,5-triene was transformed to 3,3-dialkyl-1,2,3,8-tetrahydroazulen-1-one by a two-step sequence involving the Mukaiyama aldol reaction with ketones and the subsequent Nazarov cyclization.

Original languageEnglish
Pages (from-to)2335-2343
Number of pages9
JournalSynthetic Communications
Volume30
Issue number13
DOIs
StatePublished - 2000

ASJC Scopus subject areas

  • Organic Chemistry

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