Catalyst-free photochemical reactions of alkyl dihydropyridines via modulation of chromophores and light wavelength

被引：6
|
作者：
Liu, Yanzhu [1 ]
Zhang, Zhonglin [1 ]
Wei, Zhixin [1 ]
Zhong, Zhiying [1 ]
Liu, Shiwen [2 ]
Yang, Yi [3 ]
Zeng, Xiaojun [1 ]
机构：
[1] Nanchang Univ, Sch Chem & Chem Engn, Nanchang 330031, Jiangxi, Peoples R China
[2] Yancheng Inst Technol, Coll Text & Clothing, Yancheng 224003, Jiangsu, Peoples R China
[3] Donghua Univ, Coll Chem Chem Engn & Biotechnol, 2999 North Renmin Lu, Shanghai 201620, Peoples R China
来源：
NEW JOURNAL OF CHEMISTRY | 2023年 / 47卷 / 15期
基金：
美国国家科学基金会;
关键词：
OXIDATIVE TRIFLUOROMETHYLTHIOLATION; SILVER(I) TRIFLUOROMETHANETHIOLATE; SUBSTITUENT CONSTANTS; HANTZSCH ESTERS; PHOTOREDOX; 1,4-DIHYDROPYRIDINES; REAGENTS; BONDS; ACIDS; ARYL;
D O I：
10.1039/d2nj05901k
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
This study describes an environmentally friendly strategy for thiolation and trifluoromethylthiolation of Hantzsch esters. The alkyl radical could be generated smoothly without any photocatalyst via modification of chromophores of alkyl dihydropyridines and wavelength of light. Besides, a broad alkyl dihydropyridine substrate scope and high functional group tolerance are observed. In addition, the modulation of chromophores and wavelength is applicable for other functionalizations such as halogenations and alkynylations of alkyl dihydropyridines.
引用
收藏
页码：7369 / 7374
页数：6
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