Catalytic Iron-Mediated Triene Carbocyclizations

Stereoselective Five-Membered Ring Forming Carbocyclizations

James M Takacs, Young Chan Myoung, Lawrence G. Anderson

Research output: Contribution to journalArticle

40 Citations (Scopus)

Abstract

The full details of investigations into the regiochemistry and stereochemistry of iron-catalyzed carbocyclizations of 2,7,9-decatriene derivatives to form five-membered carbocyclic ring systems are described. The roles of the allylic substituent, the alkene geometry, diene substitution, and the influence of resident stereogenic centers incorporated in the tether chain connecting the reacting 1,3-diene and alkene subunits are discussed.

Original languageEnglish (US)
Pages (from-to)6928-6942
Number of pages15
JournalJournal of Organic Chemistry
Volume59
Issue number23
DOIs
StatePublished - Nov 1 1994

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Alkenes
Iron
Stereochemistry
Substitution reactions
Derivatives
Geometry

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Catalytic Iron-Mediated Triene Carbocyclizations : Stereoselective Five-Membered Ring Forming Carbocyclizations. / Takacs, James M; Myoung, Young Chan; Anderson, Lawrence G.

In: Journal of Organic Chemistry, Vol. 59, No. 23, 01.11.1994, p. 6928-6942.

Research output: Contribution to journalArticle

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