Modification of pyrrolo[2,1-a]isoquinolines via dicarbonylation with dimethyl sulfoxide and arylacyl bromides affording 1,2-dicarbonylated pyrrolo[2,1-a]isoquinolines-Reference-Cited by-同舟云学术

Modification of pyrrolo[2,1-a]isoquinolines via dicarbonylation with dimethyl sulfoxide and arylacyl bromides affording 1,2-dicarbonylated pyrrolo[2,1-a]isoquinolines

Published:2021-12 Issue: Volume:87 Page:153548
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Chen Xiao-Hui,Xiao Xue,Li Jia-Qin,Li Wan-Zhen,Cui Hai-Lei

Funder

National Natural Science Foundation of China

Chongqing Research Program of Basic Research and Frontier Technology

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference55 articles.

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2. Pictet–Spengler reaction-based biosynthetic machinery in fungi

3. Synthesis and antimicrobial activity of new bromine-rich pyrrole derivatives related to monodeoxypyoluteorin

4. N,N′-Bisoxalamides Enhance the Catalytic Activity in Cu-Catalyzed Coupling of (Hetero)Aryl Bromides with Anilines and Secondary Amines

5. Copper-Catalyzed Coupling Reaction of (Hetero)Aryl Chlorides and Amides

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