Synthesis and Cyclization of 1-(2-Hydroxyphenyl)-2-propen-1-one Epoxides: 3-Hydroxychromanones and-flavanones versus 2-(1-Hydroxyalkyl)-3-coumaranones
T Patonay, A Lévai, C Nemes, T Timár…
Index: Patonay, Tamas; Levai, Albert; Nemes, Csaba; Timar, Tibor; Toth, Gabor; Adam, Waldemar Journal of Organic Chemistry, 1996 , vol. 61, # 16 p. 5375 - 5383
Full Text: HTML
Citation Number: 29
Abstract
Competitive α and β cyclization of 2'-hydroxychalcone epoxides affords 2-(α-hydroxybenzyl)- 3-coumaranone and/or 3-hydroxyflavanones, which depends on the conditions employed. Epoxidation of 2'-hydroxychalcones by dimethyldioxirane followed by either base-or acid- catalyzed ring closure provides a novel, general, and efficient method for the synthesis of trans-3-hydroxyflavanones, which includes also the naturally occurring derivatives. ...
Related Articles:
[Dubrovskiy, Anton V.; Larock, Richard C. Tetrahedron, 2013 , vol. 69, # 13 p. 2789 - 2798]
[Zhang, Zuhui; Pan, Chongfeng; Wang, Zhiyong Chemical Communications, 2007 , # 44 p. 4686 - 4688]
[Lopez, Cecilia Samaniego; Erra-Balsells, Rosa; Bonesi, Sergio M. Tetrahedron Letters, 2010 , vol. 51, # 33 p. 4387 - 4390]
[Sebok; Timar; Eszenyi; Patonay Journal of Organic Chemistry, 1994 , vol. 59, # 21 p. 6318 - 6321]
[Sebok; Timar; Eszenyi; Patonay Journal of Organic Chemistry, 1994 , vol. 59, # 21 p. 6318 - 6321]