Dichotomous mechanistic behavior in Narasaka-Heck cyclizations: Electron rich Pd-catalysts generate iminyl radicals

Nicholas J. Race, Adele Faulkner, Megan H. Shaw, John F. Bower

Research output: Contribution to journalArticlepeer-review

44 Scopus citations

Abstract

Pd-catalyzed cyclizations of oxime esters with pendant alkenes are subject to an unusual ligand controlled mechanistic divergence. Pd-systems modified with electron deficient phosphines (e.g. P(3,5-(CF3)2C6H3)3) promote efficient aza-Heck cyclization, wherein C-N bond formation occurs via alkene imino-palladation. Conversely, electron rich ligands, such as P(t-Bu)3, cause deviation to a SET pathway and, in these cases, C-N bond formation occurs via cyclization of an iminyl radical. A series of mechanistic experiments differentiate the two pathways and the scope of the hybrid organometallic radical cyclization is outlined. This study represents a rare example in Pd-catalysis where selection between dichotomous mechanistic manifolds is facilitated solely by choice of phosphine ligand.

Original languageEnglish (US)
Pages (from-to)1508-1513
Number of pages6
JournalChemical Science
Volume7
Issue number2
DOIs
StatePublished - 2016
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2016 The Royal Society of Chemistry.

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