Enantioselective N-heterocyclic carbene catalyzed diene regenerative (4 + 2) annulation

Alison Levens, Changhe Zhang, Lisa Candish, Craig Macdonald Forsyth, David Lupton

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26 Citations (Scopus)

Abstract

An enantioselective N-heterocyclic carbene (NHC)-catalyzed diene regenerative (4 + 2) annulation has been achieved through the use of highly nucleophilic morpholinone-derived catalysts. The reaction proceeds with good to excellent yields, high enantioselectivity (most >92% ee), and good diastereoselectivity (most >7:1). The generality of the reaction is high, with 19 examples reported. The utility of the products has been examined with subsequent derivatization in Diels–Alder reactions using electron-poor dienophiles. Furthermore, interception of the proposed β-lactone intermediate has been achieved, allowing the synthesis of compounds bearing four contiguous stereocenters with high levels of enantio- and diastereoselectivity.
Original languageEnglish
Pages (from-to)5332-5335
Number of pages4
JournalOrganic Letters
Volume17
Issue number21
DOIs
Publication statusPublished - 2015

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