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| 005 | 20250625140609.0 | ||
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| 090 | _aB-9275 | ||
| 245 | 1 | 0 | _aA convenient and biogenetic type synthesis of few naturally occurring chromeno dihydrochalcones and their in vitro antileishmanial activity |
| 490 | 0 | _vBioorganic & Medicinal Chemistry Letters, 14(15), p.3913-3916, 2004 | |
| 520 | 3 | _a20,20-Dimethyl chromeno dihydrochalcones are very rare in nature as plant secondary metabolites. Recently we have reported three such compounds from the plant Crotalaria ramosissima. Chromeno dihydrochalcones contain a 20,20-dimethyl benzopyran system, which are frequently encountered in many natural products and exhibit a variety of biological activities. We here report the strategy to conveniently synthesize naturally occurring chromeno dihydrochalcones by biogenetic type pyridine or Amberlyst-15 catalyzed chromenylation of dihydrochalcones and in vitro antileishmanial activity of chromeno dihydrochalcones and their intermediates. | |
| 700 | 1 | 2 | _aTadigoppula Narender |
| 700 | 1 | 2 | _aShweta |
| 700 | 1 | 2 | _aGupta, S. |
| 856 | 4 | 0 |
_uhttps://drive.google.com/file/d/1qX0AUR13wjkk9jwlzcnwNvaqWcTqnE1K/view?usp=drivesdk _zPara ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx |
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