An Efficient Optimization, In Situ Reduction and Cyclization Reaction for the Synthesis of Functionalized Pyrazolo[3,4‐ f ]quinolines Derivatives-Reference-Cited by-同舟云学术

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An Efficient Optimization, In Situ Reduction and Cyclization Reaction for the Synthesis of Functionalized Pyrazolo[3,4‐ f ]quinolines Derivatives

Published:2018-10-19 Issue:12 Volume:55 Page:2929-2935
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:J. Heterocyclic Chem.

Author:

Liu Jia‐Yan¹,Chen Juan²,Chen Dong‐Mei¹,Wei Ming¹,Chen Dong‐Sheng¹^ORCID

Affiliation:

1. Kangda College of Nanjing Medical University Lianyungang 222000 Jiangsu People's Republic of China

2. Lianyungang Branch College of Traditional Chinese MedicineJiangsu Union Technical Institute Lianyungang 222007 Jiangsu People's Republic of China

Funder

Science Research and Development Foundation of the Kangda College of Nanjing Medical University

Natural Science Foundation for Colleges and Universities of Jiangsu Province

Publisher

Wiley

Subject

Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.3366

Reference24 articles.

1. Quinoline: A versatile heterocyclic

2. A review on anticancer potential of bioactive heterocycle quinoline

3. Pyrazole NNRTIs 4: Selection of UK-453,061 (lersivirine) as a Development Candidate

4. New orally active PDE4 inhibitors with therapeutic potential

5. Pyrazoloheteroaryls: Novel p38α MAP kinase inhibiting scaffolds with oral activity

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Recent Progress in the Synthetic Methods of Pyrazoloquinoline Derivatives;Current Organic Chemistry;2024-01

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