An Efficient Two-Step Synthesis of 2,5-Disubstituted Oxazole Derivatives Involving Cu-Promoted Carbon-Carbon Single Bond Formation
作者:Jyotirmay Maiti、Suman Biswas、Ranjan Das
DOI:10.14233/ajchem.2016.19743
日期:——
Environment sensitive fluorescence probe to detect various organelles is emerging as an excellent tool to attract the attention of a large number of researchers around the globe. The recent developments have shown that oxazole dyes are very competent and can exhibit a useful fluorescence property in this direction. An efficient synthetic procedure towards 2,5-diaryl substituted oxazole derivatives have been reported. It is a two-step technique involving classical van Leusen protocol followed by copper-mediated coupling with aryl halides to introduce the required carbon-carbon single bond. The aryl groups are chosen in such a way so that the aryl functionalities at 2- and 5-positions of oxazole can act as acceptor and donor moiety respectively. Thus, in turn, the extended conjugation from donor moiety to acceptor moiety via the oxazole ring is set up therein. The oxazole derivatives were characterized by various spectroscopic measurements like NMR, IR and MS.
环境敏感荧光探针用于检测各种细胞器,正成为吸引全球众多研究者关注的优秀工具。最近的发展表明,噁唑染料非常有效,并且在这方面可以展示出有用的荧光特性。已经报道了一种高效的合成途径用于制备2,5-二芳基取代的噁唑衍生物。这是一种两步技术,涉及经典的范·吕森法(van Leusen protocol),随后与芳基卤化物进行铜介导的耦合,以引入所需的碳-碳单键。芳基的选择方式使得噁唑在2位和5位的芳基官能团分别可以作为受体和供体部分。因此,供体部分通过噁唑环与受体部分之间建立了扩展共轭关系。噁唑衍生物通过各种光谱测量(如NMR、IR和MS)进行了表征。