Hypervalent Iodine Reagents in Palladium-Catalyzed Oxidative Cross-Coupling Reactions

被引:29
作者
Shetgaonkar, Samata E. [1 ]
Singh, Fateh V. [1 ]
机构
[1] Vellore Inst Technol, Div Chem, Sch Adv Sci, Chennai, Tamil Nadu, India
关键词
hypervalent iodine reagents; palladium; oxidant; catalyst; bond formation; C-H BONDS; C(SP(2))-H BONDS; DIRECTING GROUP; INTERMOLECULAR AMINOACETOXYLATION; UNACTIVATED C(SP(3))-H; CYCLIZATION-OXIDATION; TERMINAL OLEFINS; DIRECT ARYLATION; ETHER SYNTHESIS; ALKENES;
D O I
10.3389/fchem.2020.00705
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hypervalent iodine compounds are valuable and versatile reagents in synthetic organic chemistry, generating a diverse array of useful organic molecules. Owing to their non-toxic and environmentally friendly features, these reagents find potential applications in various oxidative functionalization reactions. In recent years, the use of hypervalent iodine reagents in palladium-catalyzed transformations has been widely studied as they are strong electrophiles and powerful oxidizing agents. For instance, extensive work has been carried out in the field of C-H bond functionalization via Pd-catalysis using hypervalent iodine reagents as oxidants. In addition, nowadays, iodine(III) reagents have been frequently employed as arylating agents in Pd-catalyzed C-H arylation or Heck-type cross-coupling reactions. In this review, recent advancements in the area of palladium-catalyzed oxidative cross-coupling reactions using hypervalent iodine reagents are summarized in detail.
引用
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页数:25
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