Stoichiometry-controlled cycloaddition of nitrilimines with unsymmetrical exocyclic dienones: microwave-assisted synthesis of novel mono- and dispiropyrazoline derivatives-Reference-Cited by-同舟云学术

Stoichiometry-controlled cycloaddition of nitrilimines with unsymmetrical exocyclic dienones: microwave-assisted synthesis of novel mono- and dispiropyrazoline derivatives

Published:2016 Issue:55 Volume:6 Page:49868-49875
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Gazzeh Houda¹²³⁴⁵,Boudriga Sarra¹²³⁴⁵,Askri Moheddine¹²³⁴⁵,Khatyr Abderrahim⁶⁷⁸⁹,Knorr Michael⁶⁷⁸⁹,Strohmann Carsten¹⁰¹¹¹²,Golz Christopher¹⁰¹¹¹²,Rousselin Yoann¹³¹⁴¹⁵⁹,Kubicki Marek M.¹³¹⁴¹⁵⁹

Affiliation:

1. Laboratory of Heterocyclic Chemistry Natural Product and Reactivity/CHPNR

2. Department of Chemistry

3. Faculty of Science of Monastir

4. 5000 Monastir

5. Tunisia

6. Institut UTINAM – UMR CNRS 6213

7. Université de Franche-Comté

8. 25030 Besançon

9. France

10. Technische Universität Dortmund

11. 44221 Dortmund

12. Germany

13. Institute of Molecular Chemistry – UMR CNRS 6302

14. University of Bourgogne

15. F-21078 Dijon

Abstract

The Microwave-assisted 1,3-dipolar cycloaddition of (E,E)-1,3-bisarylidenetetral-2-ones with nitrilimines affords a series of mono- and dispiropyrazolines in good to excellent yields.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/RA/C6RA09703K

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1. Synthesis and biological evaluation of novel pyrazoline derivatives as potent anti-inflammatory agents

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4. Synthesis, biological evaluation and molecular docking of some substituted pyrazolines and isoxazolines as potential antimicrobial agents

5. Thiophene and benzodioxole appended thiazolyl-pyrazoline compounds: Microwave assisted synthesis, antimicrobial and molecular docking studies

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