Synthesis of syn - and enantioenriched anti -β-amino alcohols by highly diastereoselective borono-Mannich allylation reactions.
Philip J ChevisThanika PromchaiChristopher RichardsonThunwadee LimtharakulStephen G PynePublished in: Chemical communications (Cambridge, England) (2022)
A highly diastereoselective method for the synthesis of syn -β-amino alcohols and enantioenriched anti -β-amino alcohols has been developed involving α-hydroxyl aldehydes and chiral α-phenylaminoxyaldehydes or α-benzoyloxyaldehydes, respectively in Petasis borono-Mannich allylation reactions. This study broadens the scope and utility of the Petasis reaction to include pinacol allylboronate and highlights its unique reactivity and stereochemical outcomes.