Visible-light-induced decarboxylative cascade cyclization of acryloylbenzamides with N-hydroxyphthalimide esters via EDA complexes

被引:6
|
作者
Li, Qing [1 ]
Zhu, Zhi-Qiang [1 ]
Zhang, Wen-Yi [1 ]
Le, Zhang-Gao [1 ]
Xie, Zong-Bo [1 ]
机构
[1] East China Univ Technol, Sch Chem & Mat Sci, Jiangxi Prov Key Lab Synthet Chem, Nanchang 330013, Jiangxi, Peoples R China
关键词
REDOX-ACTIVE ESTERS; METAL-FREE; SELECTIVE INHIBITORS; METHACRYLOYL BENZAMIDES; N-(ACYLOXY)PHTHALIMIDES; CONSTRUCTION; POLYMERASE; DESIGN; POTENT;
D O I
10.1039/d3ob01970e
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A visible-light-induced decarboxylative cascade reaction of acryloylbenzamides with alkyl N-hydroxyphthalimide (NHP) esters for the synthesis of various 4-alkyl isoquinolinediones mediated by triphenylphosphine (PPh3) and sodium iodide (NaI) was developed. This operationally simple protocol proceeded via the photoactivation of electron donor-acceptor (EDA) complexes between N-hydroxyphthalimide esters and NaI/PPh3, resulting in multiple carbon-carbon bond formations without the use of precious metal complexes or synthetically elaborate organic dyes, which provided an alternative practical approach to synthesize diverse isoquinoline-1,3(2H,4H)-dione derivatives.
引用
收藏
页码:965 / 969
页数:5
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