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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

PMID17217265

摘要

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].

材料

货号

品牌

产品描述

663131

Sigma-Aldrich

2-二环己基磷-2′,6′-二异丙氧基-1,1′-联苯, 98%

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