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

页码：645 / 659

页数：15

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