Skip to main navigation Skip to search Skip to main content

Ring synthesis by stereoselective, methylene-free enyne cross metathesis

  • SUNY Buffalo

Research output: Contribution to journalArticlepeer-review

44 Scopus citations

Abstract

Tandem enyne metathesis between 1-alkynes and 1,5-cyclooctadiene or all-cis-1,4-polybutadiene resulted in a direct, one-step ring synthesis of cyclohexadienes by methylene-free metathesis. The use of methylene-free metathesis conditions provided apparent Z-selectivity in the intermolecular enyne metathesis step.

Original languageEnglish
Pages (from-to)8110-8111
Number of pages2
JournalJournal of the American Chemical Society
Volume126
Issue number26
DOIs
StatePublished - Jul 7 2004

Fingerprint

Dive into the research topics of 'Ring synthesis by stereoselective, methylene-free enyne cross metathesis'. Together they form a unique fingerprint.

Cite this