Organic Letters · 2020 · 18 citations · 58 references
An efficient and mild method for reductive C-O bond cleavage of lignin β-O-4 ketone models was developed to afford the corresponding ketones and phenols with <b>PDI</b>-CoCl<sub>2</sub> as the precatalyst and diboron reagent as the reductant. The synthetic utility of the methodology was demonstrated by depolymerization of a polymeric model and gram-scale transformation. Mechanistic studies suggested that this transformation involves steps of carbonyl insertion, 1,2-Brook type rearrangement, β-oxygen elimination, and rate-limiting regeneration of the catalytic active Co-B species.
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Molecular rearrangements of organosilicon compounds
Accounts of Chemical Research · 1974 · 707 citations
Chemoselective Metal-Free Aerobic Alcohol Oxidation in Lignin
Alireza Rahimi, Ali Azarpira, Hoon Kim et al. · Journal of the American Chemical Society · 2013 · 633 citations