Synthesis of 1-azaxanthones by condensation of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with 3-(cyano)benzopyrylium triflates and subsequent domino ‘retro-Michael/nitrile-addition/heterocyclization’ reaction
作者:Muhammad A. Rashid、Nasir Rasool、Bettina Appel、Muhammad Adeel、Vahuni Karapetyan、Satenik Mkrtchyan、Helmut Reinke、Christine Fischer、Peter Langer
DOI:10.1016/j.tet.2008.02.105
日期:2008.5
Functionalized 1-azaxanthones (5-oxo-5H-[1]-benzopyrano[2,3-b]pyridines) were prepared by TMSOTf-mediated condensation of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with 3-cyanochromones and subsequent base-mediated domino ‘retro-Michael/nitrile-addition/heterocyclization’ reaction.
通过TMSOTf介导的1,3-双(三甲基甲硅烷氧基)-1,3-丁二烯与3的缩合反应制备功能化的1-azaxanthones(5-oxo-5 H- [1]-苯并吡喃并[2,3- b ]吡啶)。 -氰基色酮和随后的碱基介导的多米诺骨牌“复古迈克尔/腈加成/杂环化”反应。