Primary Alcohols from Terminal Olefins: Formal Anti-Markovnikov Hydration via Triple Relay Catalysis

被引:174
作者
Dong, Guangbin [1 ]
Teo, Peili [1 ,2 ]
Wickens, Zachary K. [1 ]
Grubbs, Robert H. [1 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Arnold & Mabel Beckman Labs Chem Synth, Pasadena, CA 91125 USA
[2] Inst Chem & Engn Sci, Singapore 627833, Singapore
基金
美国国家科学基金会;
关键词
WACKER REACTION; ALKENES; OXIDATION; ALKYNES; ALDEHYDES; WATER; REGIOSELECTIVITY; STYRENES; AMINES; BOND;
D O I
10.1126/science.1208685
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Alcohol synthesis is critical to the chemical and pharmaceutical industries. The addition of water across olefins to form primary alcohols (anti-Markovnikov olefin hydration) would be a broadly useful reaction but has largely proven elusive; an indirect hydroboration/oxidation sequence requiring stoichiometric borane and oxidant is currently the most practical methodology. Here, we report a more direct approach with the use of a triple relay catalysis system that couples palladium-catalyzed oxidation, acid-catalyzed hydrolysis, and ruthenium-catalyzed reduction cycles. Aryl-substituted terminal olefins are converted to primary alcohols by net reaction with water in good yield and excellent regioselectivity.
引用
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页码:1609 / 1612
页数:4
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