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1,4-Dithiane-2,5-diol in the synthesis of thiophenes (microreview)
Chemistry of Heterocyclic Compounds ( IF 1.4 ) Pub Date : 2018-08-06 , DOI: 10.1007/s10593-018-2309-8 Seyed Sajad Sajadikhah , Malek Taher Maghsoodlou
![](//media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-018-2309-8/MediaObjects/10593_2018_2309_Figb_HTML.jpg)
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This microreview provides insight on the selected methods of thiophene synthesis starting from 1,4-dithiane-2,5-diol including K2CO3- and DABCO-catalyzed reactions, cyclopropane-based reactions, heterocyclization of alkynones, tandem Michael – intramolecular Henry reaction, Gewald reaction and thiophene ring construction as a part of fused and polycyclic structures. Microreview covers literature from 2010 to 2017.![](//media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-018-2309-8/MediaObjects/10593_2018_2309_Figd_HTML.jpg)
中文翻译:
1,4-二硫代-2,5-二醇在噻吩的合成中的应用
![](//media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-018-2309-8/MediaObjects/10593_2018_2309_Figb_HTML.jpg)
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这份微综述提供了从1,4-二噻吩-2,5-二醇(包括K 2 CO 3-和DABCO催化的反应,环丙烷基的反应,炔烃的杂环化,串联的Michael-分子内的亨利)开始的噻吩合成方法的见解。反应,Gewald反应和噻吩环结构作为稠合和多环结构的一部分。Microreview涵盖2010年至2017年的文献。![](//media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-018-2309-8/MediaObjects/10593_2018_2309_Figd_HTML.jpg)
更新日期:2018-08-06
Chemistry of Heterocyclic Compounds ( IF 1.4 ) Pub Date : 2018-08-06 , DOI: 10.1007/s10593-018-2309-8 Seyed Sajad Sajadikhah , Malek Taher Maghsoodlou
![](http://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-018-2309-8/MediaObjects/10593_2018_2309_Figb_HTML.jpg)
![](http://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-018-2309-8/MediaObjects/10593_2018_2309_Figc_HTML.jpg)
![](http://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-018-2309-8/MediaObjects/10593_2018_2309_Figd_HTML.jpg)
中文翻译:
![](https://scdn.x-mol.com/jcss/images/paperTranslation.png)
1,4-二硫代-2,5-二醇在噻吩的合成中的应用
![](http://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-018-2309-8/MediaObjects/10593_2018_2309_Figb_HTML.jpg)
![](http://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-018-2309-8/MediaObjects/10593_2018_2309_Figc_HTML.jpg)
![](http://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-018-2309-8/MediaObjects/10593_2018_2309_Figd_HTML.jpg)