Catalytic hydroboration of carbonyl derivatives by using phosphinimino amide ligated magnesium complexes?

Dalton Transactions Pub Date: 2021-08-14 DOI: 10.1039/D1DT00143D

Abstract

Reduction of carbonyl derivatives by using Earth-abundant, cheap, and environmentally benign metal-based catalysts through an atom-efficient method is a challenging task. Herein, we report the synthesis and characterization of dinuclear magnesium complexes 1–3 chelated by a phosphinimino amide skeleton. In combination with pinacolborane (HBpin) as a reducing agent, complex 1 bearing an ortho-methyl substituent on the phenyl ring of the ligand showed excellent reduction capability for a broad range of carbonyl derivatives under mild reaction conditions. Aldehydes, ketones, and acrolein substrates were efficiently reduced to the corresponding alkoxy-borane products with a record high TOF. Besides, acrolein derivatives were exclusively reduced to 1,2-regioselective products. Using two equiv. of HBpin, ester substrates were reduced to two kinds of alkoxy-borane products. Carbonate reduction accomplished by using complex 1 and three equiv. of HBpin afforded diols and a methanol precursor, respectively. When chiral substrates such as (S)-1,2-propanediol carbonate and L-lactide or polymeric P(L-LA) were employed, the chirality was almost retained in their reductive products.

Graphical abstract: Catalytic hydroboration of carbonyl derivatives by using phosphinimino amide ligated magnesium complexes
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