| 000 | 01251nam a22002657a 4500 | ||
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| 003 | ZW-GwMSU | ||
| 005 | 20250321065513.0 | ||
| 008 | 250321b |||||||| |||| 00| 0 eng d | ||
| 022 | _a09743626 | ||
| 040 |
_aMSU _bEnglish _cMSU _erda |
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| 050 | 0 | 0 | _aQD31 JOU |
| 100 | 1 |
_aDhinakaran, Isaivani _eauthor |
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| 245 | 1 | 0 |
_aOne-pot synthesis of N-aryl 1,4-dihydropyridine derivatives and their biological activities / _ccreated by Isaivani Dhinakaran, Vediappen Padmini and Nattamai Bhuvanesh |
| 264 | 1 |
_aBangalore : _bSpringer, _c2015. |
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| 336 |
_2rdacontent _atext _btxt |
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| 337 |
_2rdamedia _aunmediated _bn |
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| 338 |
_2rdacarrier _avolume _bnc |
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| 440 |
_aJournal of chemical sciences _vVolume 127, number 12, |
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| 520 | 3 | _aHighly efficient, one pot synthesis of N-aryl, 1,4-dihydopyridines was carried out by four component reaction. Synthesized 1,4-dihydropyridines were screened for their cytotoxicity against A549 cell line. All the synthesized compounds exhibited better DPPH radical scavenging activity. | |
| 650 |
_aOne-pot synthesis; _vEnamine _xRadical scavenging |
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| 700 | 1 |
_aPadmini, Vediappen _eco author |
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| 700 | 1 |
_aBhuvanesh, Nattamai _eco author |
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| 856 | _uhttps://doi.org/10.1007/s12039-015-0983-y | ||
| 942 |
_2lcc _cJA |
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| 999 |
_c169424 _d169424 |
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