Synthesis of C-glycosides enabled by palladium-catalyzed glycosylation reactions

被引:4
作者
Tong, Wenli [1 ]
Wan, Jie-Ping [1 ]
Liu, Jianchao [1 ]
机构
[1] Jiangxi Normal Univ, Inst Flow Chem & Engn, Coll Chem & Mat, Natl Engn Res Ctr Carbohydrate Synth, Nanchang 330022, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
STEREOSELECTIVE-SYNTHESIS; H FUNCTIONALIZATION; NATURAL-PRODUCTS; CHEMICAL-SYNTHESIS; O-GLYCOSYLATION; BOND FORMATION; ARYL; TRYPTOPHAN; ARYLATION; RING;
D O I
10.1039/d4qo01619j
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
C-Glycosides are a privileged class of carbohydrates that exhibit remarkable biological and pharmaceutical activities. Transition metal-catalyzed cross-coupling reactions are powerful tools for the efficient and rapid construction of C-C bonds. Among various transition-metal catalyzed methods, palladium-catalyzed C-glycosylation is an effective and reliable approach to synthesize C-glycosides and involves the reaction of glycosyl donors and various reaction partners via C-C glycosidic bond formation under mild conditions with high regio/stereo-selectivities. In this review, palladium-catalyzed C-glycosylation reactions from 2020 to 2024 are summarized and discussed in detail, with focus on the synthesis of C-aryl glycosides, C-alkyl glycosides, C-alkenyl glycosides, and other functionalized C-glycosides. Some representative synthetic strategies and their transformation application along with reaction mechanisms are also highlighted.
引用
收藏
页码:6918 / 6941
页数:24
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