Peng, L (Peng, Long)[ 1 ] ; Li, YQ (Li, Yuqiang)[ 1 ] ; Li, YY (Li, Yangyang)[ 1 ] ; Wang, W (Wang, Wang)[ 1 ] ; Pang, HL (Pang, Hailiang)[ 1 ] ; Yin, GY (Yin, Guoyin)[ 1 ]
1,1-Diarylalkanes are important structural frameworks which are widespread in biologically active molecules. Herein, we report a reductive relay cross-coupling of alkyl bromides with aryl bromides by nickel catalysis with a simple nitrogen-containing ligand. This method selectively affords 1,1-diarylalkane derivatives with good to excellent yields and regioselectivity.
作者关键词:alkyl electrophiles; beta-hydride elimination; 1,1-diarylalkanes; migratory cross-coupling; high-valent nickel
KeyWords Plus:UNACTIVATED TERTIARY ALKYL; NEGISHI ARYLATIONS; HALIDES; ELECTROPHILES; REMOTE; FUNCTIONALIZATION; SECONDARY; 1,1-DIARYLALKANES; CARBOXYLATION; DIARYLALKANES
通讯作者地址: Yin, GY (通讯作者)
Wuhan Univ, Inst Adv Studies, Wuhan 430072, Hubei, Peoples R China. |
地址:
[ 1 ] Wuhan Univ, Inst Adv Studies, Wuhan 430072, Hubei, Peoples R China |
电子邮件地址:yinguoyin@whu.edu.cn
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