Efficient Construction of a 3C-Xanthone-Linked 3C-Chromone Scaffold by Novel Double Michael Additions and Cyclizations
摘要:
A novel base-promoted cascade reaction of 2-methyl-3-(1-alkynyl)chromones to produce a 3C-xanthone-linked 3C-chromone scaffold has been developed. This tandem process involves multiple reactions such as Michael additions/cyclizations under mild conditions without a transition metal catalyst and inert atmosphere.
An Efficient Approach to Functionalized Benzo[<i>a</i>]xanthones through Reactions of 2-Methyl-3-(1-alkynyl)chromones with Electron-Deficient Chromone-Fused Dienes
作者:Jian Gong、Fuchun Xie、Hong Chen、Youhong Hu
DOI:10.1021/ol101496w
日期:2010.9.3
An efficienttandem process was developed to synthesize diversified benzo[a]xanthones from 2-methyl-3-(1-alkynyl)chromones with electron-deficient chromone-fused dienes. This unusual reaction, involving multiple steps and not requiring the use of transition metal catalysts or an inert atmosphere, results in the formation of three new C−C bonds and one C−O bond.
开发了一种有效的串联方法,以从2-甲基-3-(1-炔基)色酮与电子不足的色酮稠合二烯合成多种苯并[ a ]氧杂蒽。这种不寻常的反应涉及多个步骤,不需要使用过渡金属催化剂或惰性气氛,导致形成三个新的C-C键和一个C-O键。
CuBr-catalyzed cascade reaction of 2-substituted-3-(1-alkynyl)chromones to synthesize functionalized 3-acylfurans
作者:Liping Huang、Feng Hu、Qingdong Ma、Youhong Hu
DOI:10.1016/j.tetlet.2013.04.070
日期:2013.6
A highly efficient CuBr-catalyzed domino reaction of 2-substituted-3-(1-alkynyl)chromones to synthesize functionalized 3-acylfurans has been developed. The reaction is mild, environmentally friendly and easily handled without the necessity for dry solvents and inert atmosphere. (C) 2013 Elsevier Ltd. All rights reserved.
Efficient Construction of a 3<i>C</i>-Xanthone-Linked 3<i>C</i>-Chromone Scaffold by Novel Double Michael Additions and Cyclizations
作者:Fuchun Xie、Hong Chen、Youhong Hu
DOI:10.1021/ol101100d
日期:2010.7.2
A novel base-promoted cascade reaction of 2-methyl-3-(1-alkynyl)chromones to produce a 3C-xanthone-linked 3C-chromone scaffold has been developed. This tandem process involves multiple reactions such as Michael additions/cyclizations under mild conditions without a transition metal catalyst and inert atmosphere.