DABSO-Based, Three-Component, One-Pot Sulfone Synthesis

被引:191
作者
Deeming, Alex S. [1 ]
Russell, Claire J. [2 ]
Hennessy, Alan J. [2 ]
Willis, Michael C. [1 ]
机构
[1] Univ Oxford, Dept Chem, Chem Res Lab, Oxford OX1 3TA, England
[2] Syngenta, Jealotts Hill Int Res Ctr, Bracknell RG42 6EY, Berks, England
基金
英国工程与自然科学研究理事会;
关键词
PALLADIUM-CATALYZED AMINOSULFONYLATION; ARYL SULFONES; BIOLOGICAL-ACTIVITY; INHIBITORS; EFFICIENT; ALKYLATION; ARYLATION; OXIDATION; ALDEHYDES; HALIDES;
D O I
10.1021/ol403122a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The addition of Grignard reagents or organolithium reagents to the SO2-surrogate DABSO generates a diverse set of metal sulfinates, suitable for direct conversion to sulfone products. The metal sulfinates can be trapped in situ with a wide range of C-electrophiles, including alkyl, allyl, and benzyl halides, epoxides, and (hetero)aryliodoniums.
引用
收藏
页码:150 / 153
页数:4
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