Synthesis and spectroscopic characterization of some chromanochalcones and their dihydro derivatives

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Srinivasa Rao, M.; Kotesh, J.; Narukulla, R.; Duddeck, H.: Synthesis and spectroscopic characterization of some chromanochalcones and their dihydro derivatives. In: Arkivoc 2004 (2004), Nr. 14, S. 96-102

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To cite the version in the repository, please use this identifier: https://doi.org/10.15488/1923

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Abstract:
Synthesis of naturally occurring 6-(α,β-dihydrocinnamoyl)-3,4-dihydro-2H-chromanes has been carried out by the reaction of 6-acetyl-3,4-dihydro-2H-chromanes with methoxybenzaldehydes followed by hydrogenation of the resulting 6-cinnamoyl-3,4-dihydro-2H-chromanes.
License of this version: CC BY-NC 3.0 Unported - https://creativecommons.org/licenses/by-nc/3.0
Publication type: Article
Publishing status: publishedVersion
Publication date: 2004
Keywords english: Chromano dihydrochalcones, Chromanochalcones, Hydrogenation, NMR spectroscopy, 1 (5 hydroxy 2,2 dimethyl 3,4 dihydro 2h chromen 6 yl) 3 (2,4,5 trimethoxyphenyl)prop 2 en 1 one, 1 (5 hydroxy 2,2 dimethyl 3,4 dihydro 2h chromen 6 yl) 3 (2,4,5 trimethoxyphenyl)propan 1 one, 1 (5 hydroxy 2,2 dimethyl 3,4 dihydro 2h chromen 6 yl) 3 (4 methoxyphenyl)prop 2 en 1 one, 1 (5 hydroxy 2,2 dimethyl 3,4 dihydro 2h chromen 6 yl) 3 (4 methoxyphenyl)propan 1 one, 1 (5 hydroxy 2,2 dimethyl 3,4 dihydro 2h chromen 6 yl)ethanone, 1 (7 hydroxy 2,2 dimethyl 3,4 dihydro 2h chromen 6 yl) 3 (2,4,5 trimethoxyphenyl)prop 2 en 1 one, 1 (7 hydroxy 2,2 dimethyl 3,4 dihydro 2h chromen 6 yl) 3 (4 methoxyphenyl)prop 2 en 1 one, 1 (7 hydroxy 2,2 dimethyl 3,4 dihydro 2h chromen 6 yl) 3 (4 methoxyphenyl)propan 1 one, 1 (7 hydroxy 2,2 dimethyl 3,4 dihydro 2h chromen 6 yl)ethanone, benzaldehyde derivative, chalcone derivative, chroman derivative, unclassified drug, article, carbon nuclear magnetic resonance, chemical reaction kinetics, drug synthesis, hydrogenation, proton nuclear magnetic resonance
DDC: 540 | Chemie

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