Issue 1, 2014

Ultrasound-promoted synthesis of bi-, tri- and tetrapodal polyhydroquinolines, 1,4-dihydropyridines and the corresponding pyridines

Abstract

Bi-, tri- and tetrapodal polyhydroquinolines and 1,4-dihydropyridines were synthesised by the reaction of various alkylating agents with polyhydroquinolines and 1,4-dihydropyridines under sonication conditions. These were in turn converted to the corresponding pyridines also using sonication. Sonication produced higher yields in a faster reaction time. All the synthesized compounds were characterized using spectral data.

Graphical abstract: Ultrasound-promoted synthesis of bi-, tri- and tetrapodal polyhydroquinolines, 1,4-dihydropyridines and the corresponding pyridines

Supplementary files

Article information

Article type
Paper
Submitted
15 Sep 2013
Accepted
02 Oct 2013
First published
19 Nov 2013

RSC Adv., 2014,4, 39-46

Ultrasound-promoted synthesis of bi-, tri- and tetrapodal polyhydroquinolines, 1,4-dihydropyridines and the corresponding pyridines

G. L. Balaji, K. Rajesh, M. Venkatesh, S. Sarveswari and V. Vijayakumar, RSC Adv., 2014, 4, 39 DOI: 10.1039/C3RA45138K

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