Recent advances in direct arylation via palladium-catalyzed aromatic C-H   activation

doi:10.1055/s-2008-1042907

CORC > 北京大学 > 化学与分子工程学院

	Recent advances in direct arylation via palladium-catalyzed aromatic C-H activation
	Li, Bi-Jie ; Yang, Shang-Dong ; Shi, Zhang-Jie
刊名	synlett
	2008
关键词	C-H activation arylation palladium catalysis acetanilide CROSS-COUPLING REACTIONS CARBON-HYDROGEN-BONDS ROOM-TEMPERATURE ARYL HALIDES REDUCTIVE ELIMINATION ORGANIC-SYNTHESIS NITROGEN ATOM COMPLEXES FUNCTIONALIZATION ARENES
DOI	10.1055/s-2008-1042907
英文摘要	Highly selective arylation catalyzed by palladium and directed by the acetamino group provides an efficient and practical protocol for constructing unique biaryl scaffolds, which could be further transformed into different structural units found in a range of natural products. 1 Introduction 2 Highly Regioselective Halogenation 3 Highly Regioselective Arylation 3.1 With Arylboronic Acids 3.2 With Trialkoxyarylsilanes 3.3 With Simple Arenes 3.4 Further Transformations 4 Conclusion.; Chemistry, Organic; SCI(E); 482; REVIEW; 7; 949-957
语种	英语
内容类型	期刊论文
源URL	[http://ir.pku.edu.cn/handle/20.500.11897/397258]
专题	化学与分子工程学院
推荐引用方式 GB/T 7714	Li, Bi-Jie,Yang, Shang-Dong,Shi, Zhang-Jie. Recent advances in direct arylation via palladium-catalyzed aromatic C-H activation[J]. synlett,2008.
APA	Li, Bi-Jie,Yang, Shang-Dong,&Shi, Zhang-Jie.(2008).Recent advances in direct arylation via palladium-catalyzed aromatic C-H activation.synlett.
MLA	Li, Bi-Jie,et al."Recent advances in direct arylation via palladium-catalyzed aromatic C-H activation".synlett (2008).