Synthesis of 3-Amino-1-(difluoromethylidene)tetralins via Relay Photocatalytic Cascade Reactions of Arylalanines and 2-Bromo-3,3,3-trifluoropropene

被引:5
|
作者
Zeng, Weidi [1 ]
Li, Linyong [2 ]
Wang, Chihao [2 ]
Wang, Duozhi [1 ]
Zhou, Lei [1 ,2 ]
机构
[1] Xinjiang Univ, Coll Chem, State Key Lab Chem & Utilizat Carbon Based Energy, Urumqi 830046, Xinjiang, Peoples R China
[2] Sun Yat Sen Univ, Sch Chem, Guangzhou 510006, Peoples R China
基金
中国国家自然科学基金;
关键词
photoredox; radical; C-F bond cleavage; gem-difluoroalkene; tetralin; REGIOSELECTIVE SYNTHESIS; RECEPTOR LIGANDS; CONSTRUCTION; ALKYLATION;
D O I
10.1002/adsc.202200612
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A relay photocatalytic cascade reaction for the synthesis of 3-amino-1-(difluoromethylidene)tetralins was described. The reaction used readily available N-Boc protected arylalanines and bulk industrial chemical 2-bromo-3,3,3-trifluoropropene (BTP) as the starting materials combining two photoredox catalytic cycles with a single photocatalyst. In the first catalytic cycle, the defluorinative coupling of N-Boc arylalanines with BTP provided 2-bromo-1,1-difluoroalkenes. In the second catalytic cycle, 2-bromo-1,1-difluoroalkenes underwent intramolecular radical cyclization by photoredox activation of C(sp(2))-Br bond, affording the desired 3-amino-tetralins bearing an exo-difluoroethylene unit in good yields. Moreover, the reactions of 3-aryl propanoic acids and BTP for the construction of 1-(difluoromethylidene)tetralins were also demonstrated.
引用
收藏
页码:3310 / 3315
页数:6
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