Iodoetherification of conformationally restricted dienyl alcohols: Unexpected formation of oxocenes by 8-endo-mode oxacyclizations

Kristen L. Stoltz, Andrea Nekane R. Alba, Frank E. McDonald, Marika B. Wieliczko, John Bacsa

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Iodine-promoted oxacyclizations of a family of conformationally restricted dienyl alcohols consistently afford oxocenes, arising from 8-endo-mode cyclizations.

Original languageEnglish (US)
Pages (from-to)1519-1526
Number of pages8
JournalHeterocycles
Volume8
Issue number2
DOIs
StatePublished - 2014

Bibliographical note

Funding Information:
This material is based upon work supported by the National Science Foundation under grant

Funding Information:
This material is based upon work supported by the National Science Foundation under grant CHE-1151304. A.N.R.A. thanks MICINN for supporting her research fellowship at Emory University.

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