Recent Advances in the Functionalization of Azulene Through Pd-Catalyzed Cross-Coupling Reactions

被引:11
|
作者
Elwahy, Ahmed H. M. [1 ]
Abdelhamid, Ismail A. [1 ]
Shaaban, Mohamed R. [1 ,2 ]
机构
[1] Cairo Univ, Fac Sci, Chem Dept, Giza, Egypt
[2] Umm Al Qura Univ, Fac Appl Sci, Chem Dept, Makkah El Mukarramah, Saudi Arabia
来源
CHEMISTRYSELECT | 2021年 / 6卷 / 47期
关键词
Pd-catalyzed C-H activation; Suzuki-Miyaura reaction; Stille-Migita reaction; Negishi reaction; Heck reaction; Sonogashira reaction; azulene; HOLE-INJECTING MATERIAL; 1ST ORGANOTIN REAGENTS; 2+2 CYCLOADDITION; DIRECT ARYLATION; REDOX BEHAVIOR; N,N,N',N'-TETRASUBSTITUTED 1,3-BIS(4-AMINOPHENYL)AZULENES; 2-SUBSTITUTED AZULENES; SUBSTITUTION-REACTIONS; CONJUGATED OLIGOMERS; ORGANIC CHROMOPHORES;
D O I
10.1002/slct.202103357
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Azulene derivatives have important physical and physicochemical features, as well as advantageous biological qualities. The metal-catalyzed processes have proven to be a highly practical method for azulene functionalization. The development in the synthesis of azulene derivatives, including (aryl)heteroaryl-substituted and hetero-fused azulene derivatives, through Pd-catalyzed coupling techniques over the previous two decades is discussed in this research. Alkyl-, alkenyl-, and alkynylazulenes synthesized via Pd-catalyzed cross-coupling processes are also included.
引用
收藏
页码:13664 / 13723
页数:60
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