A rapid and convergent synthesis of the integrastatin core

Pamela M. Tadross, Pradeep Bugga, Brian M. Stoltz

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

The tetracyclic core of the integrastatin natural products has been prepared in a convergent and rapid manner. Our strategy relies upon a palladium(ii)-catalyzed oxidative cyclization to form the central [3.3.1]-dioxabicycle of the natural product core. Overall, the core has been completed in only 4 linear steps from known compounds. © 2011 The Royal Society of Chemistry.
Original languageEnglish (US)
Pages (from-to)5354
JournalOrganic & Biomolecular Chemistry
Volume9
Issue number15
DOIs
StatePublished - 2011
Externally publishedYes

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