Novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines — Microwave-assisted synthesis and structural confinements
The one pot, three component reaction of p-hydroxy benzaldehyde, β-ketoester, and ammonium acetate afforded the corresponding monopodal 1,4-dihydropyridines as building blocks, which in turn converted into diversified novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines with different alkyla...
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Veröffentlicht in: | Canadian journal of chemistry 2011-11, Vol.89 (10), p.1236-1244 |
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container_title | Canadian journal of chemistry |
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creator | Rajesh, Kancherla Reddy, Bandapalli Palakshi Vijayakumar, Vijayaparthasarathi |
description | The one pot, three component reaction of p-hydroxy benzaldehyde, β-ketoester, and ammonium acetate afforded the corresponding monopodal 1,4-dihydropyridines as building blocks, which in turn converted into diversified novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines with different alkylating agents through conventional as well as microwave assisted reactions. The unambiguous structural confinements of the all the synthesized compounds were drawn out with the help of 2D NMR (H-H COSY and C-H COSY). |
doi_str_mv | 10.1139/v11-088 |
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The unambiguous structural confinements of the all the synthesized compounds were drawn out with the help of 2D NMR (H-H COSY and C-H COSY).</abstract><cop>Ottawa</cop><pub>NRC Research Press</pub><doi>10.1139/v11-088</doi><tpages>9</tpages></addata></record> |
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subjects | 1,4-dihydropyridines bipodes Alkylation Ammonia Ammonium Ammonium acetate Benzaldehyde bipodal-tripodal-tetrapodal 1,4-dihydropyridines Chemical compounds Chemical reactions Chemical synthesis Hantzsch pyridines Hydroxybenzaldehydes irradiation microonde microwave irradiation NMR Nuclear magnetic resonance Pyridine pyridines de Hantzsch Structure tripodes ou tétrapodes |
title | Novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines — Microwave-assisted synthesis and structural confinements |
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