Issue 56, 2014

Borax catalyzed domino reactions: synthesis of highly functionalised pyridines, dienes, anilines and dihydropyrano[3,2-c]chromenes

Abstract

Borax, an innocuous, inexpensive, and a naturally occurring material, very efficiently catalyzes the Knoevenagel condensation and Michael addition in domino fashion for the construction of highly functionalised pyridines, dienes, anilines and dihydropyrano[3,2-c]chromenes. The present protocol offers advantages in terms of higher yields, wide scope of substrates, operational simplicity, short reaction time, no requirement of workup or column chromatography, and easy access to a wide range of structurally diverse functionalized molecules of biological importance. Recycling of the catalyst and scaling up of the reactions are important attributes of this catalytic process.

Graphical abstract: Borax catalyzed domino reactions: synthesis of highly functionalised pyridines, dienes, anilines and dihydropyrano[3,2-c]chromenes

Supplementary files

Article information

Article type
Paper
Submitted
21 Apr 2014
Accepted
06 Jun 2014
First published
09 Jun 2014
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2014,4, 29750-29758

Borax catalyzed domino reactions: synthesis of highly functionalised pyridines, dienes, anilines and dihydropyrano[3,2-c]chromenes

A. Molla and S. Hussain, RSC Adv., 2014, 4, 29750 DOI: 10.1039/C4RA03627A

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