Iridium-catalysed direct C-C coupling of methanol and allenes

被引:145
|
作者
Moran, Joseph [1 ]
Preetz, Angelika [1 ]
Mesch, Ryan A. [1 ]
Krische, Michael J. [1 ]
机构
[1] Univ Texas Austin, Dept Chem & Biochem, Austin, TX 78712 USA
基金
美国国家科学基金会; 加拿大自然科学与工程研究理事会;
关键词
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.
引用
收藏
页码:287 / 290
页数:4
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