Construction of 3,4-Dihydroquinolone Derivatives through Pd-Catalyzed [4+2] Cycloaddition of Vinyl Benzoxazinanones with α-Alkylidene Succinimides

被引:4
|
作者
Yu, Ting-Ting [1 ]
Huang, Peng-Ting [1 ]
Chen, Ben-Hong [1 ]
Zhong, Ya-Jun [1 ]
Han, Bo [1 ]
Peng, Cheng [1 ]
Zhan, Gu [1 ]
Huang, Wei [1 ]
Zhao, Qian [1 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Sch Pharm, Sch Basic Med Sci, State Key Lab Southwestern Chinese Med Resources, Chengdu 611137, Peoples R China
来源
JOURNAL OF ORGANIC CHEMISTRY | 2024年 / 89卷 / 05期
基金
中国国家自然科学基金;
关键词
NITROGEN-HETEROCYCLES; 1,3-DIPOLAR CYCLOADDITION; STEREOSELECTIVE-SYNTHESIS; BENZYLIDENE SUCCINIMIDES; ASYMMETRIC CONSTRUCTION; CYCLIZATION REACTIONS; BIOLOGICAL-ACTIVITY; PALLADIUM; MELODINUS; TANDEM;
D O I
10.1021/acs.joc.3c02728
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The construction of 3,4-dihydroquinolone derivatives has attracted a considerable amount of attention due to their extensive applications in medicinal chemistry. In this study, we present the Pd-catalyzed [4+2] cycloaddition of vinyl benzoxazinanones with alpha-alkylidene succinimides for the efficient synthesis of 3,4-dihydroquinolones. This approach presents numerous advantages, including the ready availability of starting materials, mild reaction conditions without the use of additional bases, and a wide range of substrates. In particular, all of the desired products can be easily afforded in high yields (<= 99%) and excellent diastereoselectivities (>20:1). The practicality and reliability of this strategy were demonstrated by the successful scale-up synthesis and subsequent straightforward synthetic transformations.
引用
收藏
页码:3279 / 3291
页数:13
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