Highly diastereoselective synthesis of quinoline-2,5-diones and pyrazolo[3,4-b]pyridin-6(7H)-ones under microwave irradiation-Reference-Cited by-同舟云学术

Highly diastereoselective synthesis of quinoline-2,5-diones and pyrazolo[3,4-b]pyridin-6(7H)-ones under microwave irradiation

Published:2014 Issue:97 Volume:4 Page:54480-54486
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Jiang Bo¹²³⁴,Liang Yan-Bo¹²³⁴,Kong Li-Fang⁵⁶⁴,Tu Xing-Jun¹²³⁴,Hao Wen-Juan¹²³⁴,Ye Qin¹²³⁴,Tu Shu-Jiang¹²³⁴

Affiliation:

1. School of Chemistry and Chemical Engineering

2. Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials

3. Jiangsu Normal University

4. Xuzhou, P. R. China

5. Department of Basic Teaching

6. Air Force Logistic Academy

Abstract

A new and flexible three-component reaction has been established for the highly diastereoselective synthesis of bicyclic hexahydroquinoline-2,5-diones and pyrazolo[3,4-b]pyridin-6(7H)-ones.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA10096D

Reference44 articles.

1. Practical Route to a New Class of LTD4 Receptor Antagonists

2. Synthesis and Antibacterial Evaluation of Certain Quinolone Derivatives

3. Synthesis and pharmacological properties of some quinoline derivatives

4. Quinolines as potent 5-lipoxygenase inhibitors: Synthesis and biological profile of L-746,530

5. Synthesis of 4-alkoxy-2-phenylquinoline derivatives as potent antiplatelet agents

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