Synthesis of [2.2]Paracyclophane-Fused Heterocycles via Palladium-Catalyzed C-H Activation/Annulation of [2.2]Paracyclophanecarboxamides with Arynes

被引:1
|
作者
Pan, Chongqing [1 ,2 ]
Sun, Hongwei [1 ,2 ]
Du, Yonglei [1 ,2 ]
Wang, Wenbin [1 ,2 ]
Xu, Lingling [1 ,2 ]
Hu, Yu [1 ,2 ]
Zhu, Manzhou [1 ,2 ]
机构
[1] Anhui Univ, Dept Chem, Minist Educ, Hefei 230601, Anhui, Peoples R China
[2] Anhui Univ, Anhui Prov Key Lab Chem Inorgan Organ Hybrid Funct, Key Lab Struct & Funct Regulat Hybrid Mat, Ctr Atom Engn Adv Mat,Minist Educ, Hefei 230601, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
ACTIVATED DELAYED FLUORESCENCE; ISOQUINOLONE SYNTHESIS; OXIDATIVE ANNULATION; ESTER SYNTHESIS; O BOND; PLANAR; FUNCTIONALIZATION; DERIVATIVES; BENZAMIDES; RESOLUTION;
D O I
10.1021/acs.orglett.4c00472
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[2.2]Paracyclophane-fused heterocycles represent an important scaffold. Traditional approaches often suffer from tedious synthetic routes, and the development of catalytic synthesis of them remains in its infancy. Herein, by employing highly strained aryne intermediates as partners, we have developed a concise protocol by palladium-catalyzed C-H activation/annulation from [2.2]paracyclophanecarboxamide substrates. [2.2]Paracyclophane-fused quinolinone products are obtained in good yields (up to 84%). Furthermore, the utility of the process has been shown through the synthesis of [2.2]paracyclophane-fused heterocyclic catalysts. [GRAPHICS]
引用
收藏
页码:2387 / 2392
页数:6
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