Hypervalent iodine reactions utilized in carbon-carbon bond formations

被引：99

作者：

Hyatt, I. F. Dempsey ^{[1
]}

Dave, Loma ^{[1
]}

David, Navindra ^{[1
]}

Kaur, Kirandeep ^{[1
]}

Medard, Marly ^{[1
]}

Mowdawalla, Cyrus ^{[1
]}

机构：

[1] Adelphi Univ, Dept Chem & Biochem, 1 South Ave, Garden City, NY 11530 USA

来源：

ORGANIC & BIOMOLECULAR CHEMISTRY | 2019年 / 17卷 / 34期

关键词：

BIARYL COUPLING REACTION; NUCLEOPHILIC VINYLIC SUBSTITUTIONS; ENANTIOSELECTIVE ALPHA-ARYLATION; C-H; DIARYLIODONIUM SALTS; DIRECT ALKYNYLATION; DECARBOXYLATIVE ALKYNYLATION; PHOTOREDOX CATALYSIS; CARBOXYLIC-ACIDS; STEREOSELECTIVE-SYNTHESIS;

D O I：

10.1039/c9ob01267b

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Advances in hypervalent iodine chemistry have put the field on the precipice of a second golden age; the first being pioneered in the 1990s. During that period, C-C bond forming reactions would be published but rarely with the intended goal of developing a C-C bond forming methodology. More recently, the development of hypervalent iodine-guided electrophilic substitution, arylations using hypervalent iodine, and photoredox reactions with hypervalent iodine have shown great progress in the area of C-C bond formation.

引用

页码：7822 / 7848

页数：27

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