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. © 2014 The Royal Society of Chemistry.
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CITATION STYLE
Balaji, G. L., Rajesh, K., Venkatesh, M., Sarveswari, S., & Vijayakumar, V. (2014). Ultrasound-promoted synthesis of bi-, tri- and tetrapodal polyhydroquinolines, 1,4-dihydropyridines and the corresponding pyridines. RSC Advances, 4(1), 39–46. https://doi.org/10.1039/c3ra45138k
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