Free Radical Pathway Cleavage of C-O Bonds for the Synthesis of Alkylboron Compounds

被引:30
作者
Lu, Xi [1 ]
Zhang, Zhen-Qi [1 ]
Yu, Lu [2 ]
Zhang, Ben [1 ]
Wang, Bing [1 ]
Gong, Tian-Jun [1 ]
Tian, Chang-Lin [1 ,2 ,3 ]
Xiao, Bin [1 ]
Fu, Yao [1 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, CAS Key Lab Urban Pollutant Convers, Anhui Prov Key Lab Biomass Clean Energy,iChEM, Hefei 230026, Anhui, Peoples R China
[2] Chinese Acad Sci, High Field Magnet Lab, Hefei 230031, Anhui, Peoples R China
[3] Univ Sci & Technol China, Sch Life Sci, Hefei 230027, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
radical reactions; alcohols; borates; silver; cross-coupling; LITHIATION-BORYLATION METHODOLOGY; NICKEL-CATALYZED BORYLATION; CROSS-COUPLING REACTIONS; STEREOSPECIFIC SYNTHESIS; SECONDARY; TOSYLATES; TERTIARY; HALIDES; ARYL; BORON;
D O I
10.1002/cjoc.201800500
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
.Summary of main observation and conclusion We report a silver-catalyzed borylation of alkyl tosylates, which provides a new method for the synthesis of alkylboron compounds with good functional group compatibility and excellent chemoselectivity. The present work added highly polarized alkyl tosylate C-O bonds to the fairly limited number of C-O bonds able to participate in free radical cleavage pathways. The mechanistic studies suggested that in situ-generated silver(0) catalytic species were the active catalytic species and played a key role in the radical pathway cleavage of C-O bonds.
引用
收藏
页码:11 / 18
页数:8
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