Transition-Metal-Catalyzed Suzuki-Miyaura-Type Cross-Coupling Reactions of π-Activated Alcohols

被引：18
|
作者：
Akkarasamiyo, Sunisa [1 ,3 ]
Ruchirawat, Somsak [2 ,3 ]
Ploypradith, Poonsaksi [2 ,3 ]
Samec, Joseph S. M. [1 ]
机构：
[1] Stockholm Univ, Dept Organ Chem, S-10691 Stockholm, Sweden
[2] Chulabhorn Royal Acad, Chulabhorn Grad Inst, Program Chem Sci, 906 Kamphaeng Phet 6 Rd, Bangkok 10210, Thailand
[3] Chulabhorn Res Inst, Med Chem Lab, 54 Kamphaeng Phet 6 Rd, Bangkok 10210, Thailand
来源：
SYNTHESIS-STUTTGART | 2020年 / 52卷 / 05期
基金：
瑞典研究理事会;
关键词：
C-O bond activation; alcohols; cross-coupling; Suzuki-Miyaura-; catalysis; green chemistry; ARYL BORONIC ACIDS; ALLYLIC ALCOHOLS; ARYLBORONIC ACIDS; NUCLEOPHILIC-SUBSTITUTION; GREEN CHEMISTRY; PALLADIUM; ARYLATION; COMPLEXES; ISOMERIZATION; PERSPECTIVE;
D O I：
10.1055/s-0039-1690740
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The Suzuki-Miyaura reaction is one of the most powerful tools for the formation of carbon-carbon bonds in organic synthesis. The utilization of alcohols in this powerful reaction is a challenging task. This short review covers progress in the transition-metal-catalyzed Suzuki--Miyaura-type cross-coupling reaction of pi-activated alcohol, such as aryl, benzylic, allylic, propargylic and allenic alcohols, between 2000 and June 2019.
引用
收藏
页码：645 / 659
页数：15
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