Skip to main navigation Skip to search Skip to main content

Transition-Metal-Free Regioselective Alkylation of Pyridine N-Oxides Using 1,1-Diborylalkanes as Alkylating Reagents

  • Woohyun Jo
  • , Junghoon Kim
  • , Seoyoung Choi
  • , Seung Hwan Cho*
  • *Corresponding author for this work
  • Pohang University of Science and Technology

Research output: Contribution to journalJournal articlepeer-review

Abstract

Reported herein is an unprecedented base-promoted deborylative alkylation of pyridine N-oxides using 1,1-diborylalkanes as alkyl sources. The reaction proceeds efficiently for a wide range of pyridine N-oxides and 1,1-diborylalkanes with excellent regioselectivity. The utility of the developed method is demonstrated by the sequential C−H arylation and methylation of pyridine N-oxides. The reaction also can be applied for the direct introduction of a methyl group to 9-O-methylquinine N-oxide, thus it can serve as a powerful method for late-stage functionalization.

Original languageEnglish
Pages (from-to)9690-9694
Number of pages5
JournalAngewandte Chemie - International Edition
Volume55
Issue number33
DOIs
StatePublished - 2016.08.8

Keywords

  • alkylation
  • boron
  • heterocycles
  • regioselectivity
  • transition-metal-free synthesis

Fingerprint

Dive into the research topics of 'Transition-Metal-Free Regioselective Alkylation of Pyridine N-Oxides Using 1,1-Diborylalkanes as Alkylating Reagents'. Together they form a unique fingerprint.

Cite this