A concise total synthesis of (±)- and (-)-okilactomycin D

Dawen Niu, Thomas R. Hoye

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

The spirotetronate okilactomycin D (7) has been efficiently synthesized by a route featuring a substrate-controlled, diastereoselective (8:1) intramolecular Diels - Alder (IMDA) reaction of 11. The assigned absolute configuration of (-)-7 was confirmed.

Original languageEnglish (US)
Pages (from-to)828-831
Number of pages4
JournalOrganic Letters
Volume14
Issue number3
DOIs
StatePublished - Feb 3 2012

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