• Home
  • Search Results
  • Beta-aminoethyltrifluoroborates: efficient aminoethylations via Suzuki-Miyaura cross-coupling.

Beta-aminoethyltrifluoroborates: efficient aminoethylations via Suzuki-Miyaura cross-coupling.

Organic letters (2007-01-16)
Gary A Molander, Fabricio Vargas
ABSTRACT

A set of phenethylamines has been successfully prepared via Suzuki-Miyaura cross-coupling of diverse potassium beta-aminoethyltrifluoroborates with aryl halides. The potassium beta-aminoethyltrifluoroborates were easily prepared via hydroboration of enamine and enamide precursors. [reaction: see text].

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
RuPhos, 98%