Literature DB >> 24624889

A simple and efficient synthesis of substituted 2,2'-bithiophene and 2,2':5',2″-terthiophene.

Anastasia S Kostyuchenko1, Alexey M Averkov, Alexander S Fisyuk.   

Abstract

A simple and efficient approach is developed for the synthesis of substituted 2,2'-bithiophene- and 2,2':5',2″-terthiophene-5-carboxylic acids and esters which is based on thiophene ring closure in the Fiesselmann reaction. Using this method, derivatives containing a long alkyl chain with or without an end functional group or an aryl substituent can be conveniently prepared.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 24624889     DOI: 10.1021/ol500356w

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Synthesis and optical properties of new 5'-aryl-substituted 2,5-bis(3-decyl-2,2'-bithiophen-5-yl)-1,3,4-oxadiazoles.

Authors:  Anastasia Sergeevna Kostyuchenko; Tatyana Yu Zheleznova; Anton Jaroslavovich Stasyuk; Aleksandra Kurowska; Wojciech Domagala; Adam Pron; Alexander S Fisyuk
Journal:  Beilstein J Org Chem       Date:  2017-02-17       Impact factor: 2.883

2.  Synthesis of new, highly luminescent bis(2,2'-bithiophen-5-yl) substituted 1,3,4-oxadiazole, 1,3,4-thiadiazole and 1,2,4-triazole.

Authors:  Anastasia S Kostyuchenko; Vyacheslav L Yurpalov; Aleksandra Kurowska; Wojciech Domagala; Adam Pron; Alexander S Fisyuk
Journal:  Beilstein J Org Chem       Date:  2014-07-14       Impact factor: 2.883

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.