97207-23-3Relevant articles and documents
Aspergillus niger catalyzes the synthesis of flavonoids from chalcones
Alarcon, Julio,Alderete, Joel,Escobar, Carlos,Araya, Ramiro,Cespedes, Carlos L.
, p. 160 - 167 (2013/09/12)
Flavonoids, which have many biological activities and have been widely used in nature, can be artificially synthesized. However, regioselective cyclization of chalcones is difficult by chemical methods. In this study, we demonstrated that Aspergillus nige
Synthesis of chiral flavanones from tricarbonyl (η6- Arylbenzaldehyde)chromium(0)
Liu, Gui-Xiang,Wan, Yu,Zhao, Ling-Ling,Wang, Hai-Ying,Xu, Zhou,Qi, Jin-Long,Wu, Hui
, p. 7828 - 7830 (2013/09/23)
A synthesis of chiral flavanones via the condensation of tricarbonyl(η6-arylbenzaldehyde)chromium(0) and o-hydroxyacetophenone in a shorter time at room temperature have been developed. The tricarbonylchromium(0) group was removed by virtue of light and the enantioenriched flavanones was formed with highly enantioselectivity (> 95 % ee).
Cyclodehydrogenation of 2'-Hydroxychalcones with DDQ: A Simple Route for Flavones and Aurones
Imafuku, Kimiaki,Honda, Masaaki,McOmie, J. F. W.
, p. 199 - 201 (2007/10/02)
The oxidation of 2'-hydroxychalcones with 2,3-dichloro-5,6-dicyano-p-benzoquinone provides a useful synthetic route for flavones and aurones.