Highly efficient regioselective synthesis of pyrroles via a tandem enamine formation–Michael addition–cyclization sequence under catalyst- and solvent-free conditions-Reference-Cited by-同舟云学术

Highly efficient regioselective synthesis of pyrroles via a tandem enamine formation–Michael addition–cyclization sequence under catalyst- and solvent-free conditions

Published:2015 Issue:6 Volume:17 Page:3415-3423
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Vivekanand Thavaraj¹²³⁴⁵,Vinoth Perumal¹²³⁴⁵,Agieshkumar B.⁶³⁴⁵⁷,Sampath Natarajan¹²³⁴⁵,Sudalai Arumugam⁸⁹¹⁰⁷,Menéndez J. Carlos¹¹¹²¹³¹⁴¹⁵,Sridharan Vellaisamy¹²³⁴⁵

Affiliation:

1. Organic Synthesis Group

2. Department of Chemistry

3. School of Chemical and Biotechnology

4. SASTRA University

5. Thanjavur 613401

6. Department of Biotechnology

7. India

8. Chemical Engineering and Process Development Division

9. National Chemical Laboratory

10. Pune 411 008

11. Departamento de Química Orgánica y Farmacéutica

12. Facultad de Farmacia

13. Universidad Complutense

14. 28040 Madrid

15. Spain

Abstract

An efficient three-component, catalyst-, solvent-, and column chromatography-free procedure was developed for the synthesis of 3-(1H-pyrrol-3-yl)indolin-2-ones.

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/GC/C5GC00365B

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