Photomediated One-Pot Three-Component Approach Enables the Formal Direct N-Acylation/Sulfonylation and α-C-H Functionalization of 1,2,3,4-Tetrahydroisoquinoline

被引:1
|
作者
Zhang, Yun [1 ,2 ,3 ]
Zhang, Zheng-Qian [1 ,2 ,3 ]
Du, Yao [1 ,2 ,3 ]
Nie, Jia-Huan [1 ,2 ,3 ]
Wang, Yan [1 ,2 ,3 ]
Cui, Bao-Dong [1 ,2 ,3 ]
Mou, Xue-Qing [1 ,2 ,3 ]
Zhou, Ming-Qiang [1 ,4 ]
Chen, Yong-Zheng [1 ,2 ,3 ]
机构
[1] Zunyi Med Univ, Gener Drug Res Ctr Guizhou Prov, Green Pharmaceut Engn Res Ctr Guizhou Prov, Sch Pharm,Key Lab Biocatalysis & Chiral Drug Synth, Zunyi 563006, Peoples R China
[2] Zunyi Med Univ, Minist Educ, Key Lab Basic Pharmacol, Zunyi 563006, Peoples R China
[3] Zunyi Med Univ, Minist Educ, Joint Int Res Lab Ethnomed, R China, Zunyi 563006, Peoples R China
[4] Chinese Acad Sci, Chengdu Inst Organ Chem, Natl Engn Res Ctr Chiral Drugs, Chengdu 610041, Peoples R China
来源
JOURNAL OF ORGANIC CHEMISTRY | 2024年 / 89卷 / 16期
关键词
SINGLET OXYGEN GENERATION; DIRECT IMINE ACYLATION; MULTICOMPONENT REACTIONS; PHOTOREDOX CATALYSIS; DERIVATIVES; PORPHYRIN; TETRAHYDROISOQUINOLINES; IRON; DEAROMATIZATION; ISOQUINOLINES;
D O I
10.1021/acs.joc.4c01229
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
N-Acyl/sulfonyl-alpha-functionalized 1,2,3,4-tetrahydroisoquinolines (THIQs) are significant structural motifs in organic synthesis and drug discovery. However, the one-pot approach enabling direct difunctionalization of THIQs remains challenging. Herein we report a photomediated one-pot three-component strategy to access N-acyl/sulfonyl-alpha-functionalized THIQs. This method features the use of oxygen (from air) as the green oxidant, high atom and step economy, and decent structural diversity. The synthetic applicability of the method was further demonstrated via the facile construction of valuable bioactive molecules. Mechanistic studies indicated that oxidation with singlet oxygen and the acceptor-less dehydrogenation were involved in the photoredox process.
引用
收藏
页码:11513 / 11524
页数:12
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