Synthesis of highly functionalized flavones and chromones using cycloacylation reactions and C-3 functionalization. A total synthesis of hormothamnione
LW McGarry, MR Detty
Index: McGarry, Lynda W.; Detty, Michael R. Journal of Organic Chemistry, 1990 , vol. 55, # 14 p. 4349 - 4356
Full Text: HTML
Citation Number: 78
Abstract
The cycloacylations of hydroxy. and methoxy-substituted phenols with aryl-and alkylpropiolic acids using Eaton's reagent (10% phosphorus pentoxide in methanesulfonic acid) gives highly substituted flavones and chromonea in up to 63% yield. Styrylchromones were prepared from 2-methylchromones by condensation reactions of the 2-methyl group with various substituted benzaldehydes in sodium ethoxide and ethanol in almost quantitative ...
Related Articles:
[Liao, Hua-Lin; Hu, Ming-Kuan Chemical and Pharmaceutical Bulletin, 2004 , vol. 52, # 10 p. 1162 - 1165]
[Wang, Jun-Fei; Ding, Ning; Zhang, Wei; Wang, Peng; Li, Ying-Xia Helvetica Chimica Acta, 2011 , vol. 94, # 12 p. 2221 - 2230]
[Chemical and pharmaceutical bulletin, , vol. 51, # 3 p. 339 - 340]
[Tetrahedron, , vol. 64, # 32 p. 7561 - 7566]
[Chemical and pharmaceutical bulletin, , vol. 51, # 3 p. 339 - 340]