Alkoxide Activation of Aminoboranes towards Selective Amination
Moiety
Pinacol
Alkoxide
DOI:
10.1002/anie.201305098
Publication Date:
2013-09-03T13:17:16Z
AUTHORS (2)
ABSTRACT
Piece of the (inter)action: The interaction alkoxides with sp(2) Bpin (pin=pinacol) moiety in aminoboranes forms situ Lewis acid-base adduct [RO(-) →B(OR)2 N(R')2 ] which enables amino to react as a strong nucleophile several electrophiles, thus providing alcohols, β-enamino esters, and β-hydroxy amides direct remarkably selective way.
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