Copper-Catalyzed Tandem Trifluoromethylation/Semipinacol Rearrangement of Allylic Alcohols

被引:241
作者
Chen, Zhi-Min [1 ,2 ]
Bai, Wei [1 ,2 ]
Wang, Shao-Hua [1 ,2 ]
Yang, Bin-Miao [1 ,2 ]
Tu, Yong-Qiang [1 ,2 ]
Zhang, Fu-Min [1 ,2 ]
机构
[1] Lanzhou Univ, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
[2] Lanzhou Univ, Coll Chem & Chem Engn, Lanzhou 730000, Peoples R China
关键词
copper; fluorine; semipinacol rearrangement; trifluoromethylation; -trifluoromethyl ketone; ENANTIOSELECTIVE ALPHA-TRIFLUOROMETHYLATION; PD(II)-CATALYZED ORTHO-TRIFLUOROMETHYLATION; OXIDATIVE TRIFLUOROMETHYLATION; SEMIPINACOL REARRANGEMENT; NUCLEOPHILIC TRIFLUOROMETHYLATION; MEDIATED TRIFLUOROMETHYLATION; ELECTROPHILIC TRIFLUOROMETHYLATION; TERMINAL ALKENES; HIGHLY EFFICIENT; RING EXPANSION;
D O I
10.1002/anie.201304557
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tandem jump: A novel copper-catalyzed tandem trifluoromethylation/ semipinacol rearrangement reaction of allylic alcohols has been achieved under mild conditions. This reaction is valuable for the difunctionalization of alkenes through simultaneous construction of a C sp 3-CF3 bond and a quaternary carbon center, and could provide a straightforward strategy for the preparation of α-quaternary β-trifluoromethyl ketone derivatives. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:9781 / 9785
页数:5
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