Copper-Mediated Functionalization of Aryl Trifluoroborates

Sydonie D. Schimler, Melanie S. Sanford

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

This paper describes the Cu(OTf)2-mediated coupling of aryl and heteroaryl trifluoroborates with tetrabutylammonium or alkali metal salts to form C-O, C-N, and C-halogen bonds. The reactions proceed under mild conditions (often room temperature over 16 hours) with carboxylate, halide, and azide salts, all nucleophiles that have been underrepresented in the copper cross-coupling literature. Preliminary results show that copper salts bearing weakly coordinating X-type ligands are essential for enabling these transformations to proceed under mild conditions.

Original languageEnglish (US)
Article numberst-2016-r0388-l
Pages (from-to)2279-2284
Number of pages6
JournalSynlett
Volume27
Issue number15
DOIs
StatePublished - Sep 19 2016

Bibliographical note

Publisher Copyright:
© Georg Thieme Verlag Stuttgart New York.

Copyright:
Copyright 2016 Elsevier B.V., All rights reserved.

Keywords

  • azides
  • carboxylation
  • copper
  • coupling
  • halogenation

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