Conformation and photochemical properties of 3-benzoyl-4-benzylamino-7-dimethylaminocoumarin
作者:Chi-Hui Lin、Rong-Ren Chuang、Pei-Yu Kuo、Ding-Yah Yang
DOI:10.1016/j.tetlet.2013.03.016
日期:2013.5
3-Benzoyl-4-benzylamino-7-dimethylaminocoumarin was synthesized and its conformation in solid state and solution was determined. While the X-ray crystal analysis showed an aromatic pi-pi stacking interaction in the solid state, the proton NMR studies suggested the presence of an intramolecular hydrogen bonding in solution. Adjacent functional group modifications through N-methylation, reduction of carbonyl group, or replacing the coumarin moiety to dimedone, all resulted in disrupting the pi-pi stacking conformation. Upon UV irradiation, the 7-methylamino group can be oxidized by molecular oxygen to the corresponding formamide in the absence of any external photosensitizers. (C) 2013 Elsevier Ltd. All rights reserved.
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EGG, H.;KNAUSEDER, H.;MAYR, S.;SCHOPF, D., SCI. PHARM. , 59,(1991) N, C. 12
作者:EGG, H.、KNAUSEDER, H.、MAYR, S.、SCHOPF, D.
DOI:——
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