Cu(I)-Catalyzed Three-Component Annulation for the Synthesis of 3-Acyl Imidazo[1, 5-a]Pyridines from 2-Pyridinyl-Substituted p-Quinone Methides, Terminal Alkynes, and TsN3 Using O2 as the Oxygen Source-Reference-Cited by-同舟云学术

Cu(I)-Catalyzed Three-Component Annulation for the Synthesis of 3-Acyl Imidazo[1, 5-a]Pyridines from 2-Pyridinyl-Substituted p-Quinone Methides, Terminal Alkynes, and TsN₃ Using O₂ as the Oxygen Source

Published:2024-04-01 Issue:8 Volume:89 Page:5423-5433
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Chen Yan¹,Zhang Chuanhao²,Wang Kunpeng¹,Li Mengfan¹,Tang Hao¹,Cheng Wen¹,Yin Jun³,Yi Weiyin¹^ORCID

Affiliation:

1. School of Perfume and Aroma Technology, Shanghai Institute of Technology, Shanghai 201418, P. R. China

2. School of Pharmacy, East China University of Science and Technology, Shanghai 200237, P. R. China

3. Shanghai No.4 Reagent Chemical Co., Ltd., Shanghai 201512, P. R. China

Funder

Shanghai Institute of Technology

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c02876

Reference40 articles.

1. Imidazopyridine CB2 agonists: Optimization of CB2/CB1 selectivity and implications for in vivo analgesic efficacy

2. Synthesis and anticancer activity of oxindole derived imidazo[1,5-a]pyrazines

3. Antineoplastic Agents. 485. Isolation and Structure of Cribrostatin 6, a Dark Blue Cancer Cell Growth Inhibitor from the Marine Sponge Cribrochalina sp.,1a

4. Antimicrobial activity of imidazo[1,5-a]quinoxaline derivatives with pyridinium moiety

5. A highly selective ESIPT-based fluorescent probe with a large Stokes shift for the turn-on detection of cysteine and its application in living cells

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