Regioselective construction of 1,3-diaryl tetrahydroindazolones via the three-component reaction of 1,3-cyclohexanediones, β-nitrostyrenes and arylhydrazines-Reference-Cited by-同舟云学术

Regioselective construction of 1,3-diaryl tetrahydroindazolones via the three-component reaction of 1,3-cyclohexanediones, β-nitrostyrenes and arylhydrazines

Published:2018 Issue:14 Volume:16 Page:2456-2463
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wang Ting¹²³⁴,Qing Xushun¹²³⁴,Dai Chenlu¹²³⁴,Su Zhenjie¹²³⁴,Wang Cunde¹²³⁴^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering

2. Yangzhou University

3. Yangzhou 225002

4. P. R. China

Abstract

1,5,6,7-Tetrahydro-4H-indazol-4-one derivatives were synthesized effectively via the regioselective three-component reactions of substituted β-nitrostyrenes, 1,3-cyclohexanediones and phenylhydrazines.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB00304A

Reference46 articles.

1. Syntheses and antiinflammatory actions of 4,5,6,7-tetrahydroindazole-5-carboxylic acids

2. Pharmacological Properties of Indazole Derivatives: Recent Developments

3. Nonsteroidal antiinflammatory agents—part 2 antiinflammatory, analgesic and antipyretic activity of some substituted 3-pyrazolin-5-ones and 1,2,4,5,6,7-3H-hexahydroindazol-3-ones