ALDEHYDE OXIDATION LEVEL;
FORMING TRANSFER HYDROGENATION;
CARBON QUATERNARY CENTERS;
ALLYL METAL REAGENTS;
ALPHA;
BETA-UNSATURATED KETONES;
ALCOHOL;
MECHANISM;
ACETATE;
2,2,3-TRIMETHYLBUTANE;
HYDROACYLATION;
D O I:
10.1038/NCHEM.1001
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Methanol is an abundant (35 million metric tons per year), renewable chemical feedstock, yet its use as a one-carbon building block in fine chemical synthesis is highly underdeveloped. Using a homogeneous iridium catalyst developed in our laboratory, methanol engages in a direct C-C coupling with allenes to furnish higher alcohols that incorporate all-carbon quaternary centres, free of stoichiometric by-products. A catalytic mechanism that involves turnover-limiting methanol oxidation, a consequence of the high energetic demand of methanol dehydrogenation, is corroborated through a series of competition kinetics experiments. This process represents the first catalytic C-C coupling of methanol to provide discrete products of hydrohydroxymethylation.