Nascent developments in main group element-catalyzed hydrosilylation and dehydrogenative silylation of alkenes and alkynes

被引:6
|
作者
Vignesh, Arumugam [1 ,2 ]
Liu, Jiahao [1 ]
Wang, Zhe [1 ,3 ]
Liu, Yan [1 ,3 ]
Ke, Zhuofeng [2 ]
机构
[1] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou 510006, Peoples R China
[2] Sun Yat Sen Univ, Sch Mat Sci & Engn, PCFM Lab, Guangzhou 510275, Peoples R China
[3] Guangdong Prov Key Lab Plant Resources Biorefinery, Guangzhou 510275, Peoples R China
基金
中国国家自然科学基金;
关键词
RING-OPENING POLYMERIZATION; H BOND ADDITION; CATIONIC ALUMINUM; MARKOVNIKOV HYDROSILYLATION; TERMINAL ALKYNES; METAL-COMPLEXES; RECENT PROGRESS; HYDRIDE; OLEFINS; REACTIVITY;
D O I
10.1039/d3qo01777j
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Hydrosilylation and dehydrogenative silylation of alkenes and alkynes are vital transformations in organic synthesis and have garnered significant attention due to their widespread applications in the preparation of organosilicon materials. Among the catalysts used for hydrosilylation and dehydrogenative silylation reactions, main group elements have emerged as promising alternatives to transition metals due to their abundance, low cost, and minimal toxicity. This review article provides an exhaustive survey of recent advancements in the main group element-catalyzed hydrosilylation and dehydrogenative silylation of alkenes and alkynes. The survey encompasses an in-depth analysis of the diverse catalytic systems developed over the years, highlighting mechanistic insights and their distinct chemo-, regio-, and stereoselectivity. Furthermore, the challenges and limitations researchers face in the field have been addressed, including catalyst design, stability, and substrate compatibility. Nascent developments in the main group element-catalyzed hydrosilylation of alkenes and alkynes.
引用
收藏
页码:576 / 596
页数:21
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