Literature DB >> 18007428

Reactions of substituted furan-2-carboxaldehydes and furo[b]pyrrole type aldehydes with benzothiazolium salts.

Zita Puterová1, Alzbeta Krutosíková, Antonín Lycka, Tatiana Durceková.   

Abstract

A series of new push-pull compounds were synthesised by reaction of 5-aryl- furan-2-carboxaldehydes and furo[b]pyrrole type aldehydes with benzothiazolium salts. These new condensation products represent highly conjugated systems that have potential biological activity. The reaction of furo[b]pyrrole type aldehydes with benzothiazolium salts give potential precursors of cyanine dyes.

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Year:  2004        PMID： 18007428      PMCID： PMC6147356          DOI： 10.3390/90400241

Source DB:  PubMed          Journal:  Molecules        ISSN： 1420-3049            Impact factor:   4.411


  4 in total

1.  Studies on arylfuran derivatives. Part XI. Synthesis, characterisation and biological studies on some Mannich bases carrying 2,4-dichlorophenylfurfural moiety.

Authors:  B S Holla; B S Rao; K Shridhara; P M Akberali
Journal:  Farmaco       Date:  2000-05

2.  Synthesis and antimycobacterial activity of some new 3-heterocyclic substituted chromones.

Authors:  R Gasparová; M Lácová; H M el-Shaaer; Z Odlerová
Journal:  Farmaco       Date:  1997-04

3.  Synthesis, antimicrobial testing and QSAR study of new 2-phenylethenylbenzothiazolium salts substituted by cyclic amines.

Authors:  P Magdolen; P Zahradník; P Foltínová
Journal:  Pharmazie       Date:  2000-11       Impact factor: 1.267

4.  Reaction of substituted furan-2-carboxaldehydes and furo[b]pyrrole type aldehydes with hippuric acid.

Authors:  Zita Puterová; Heinz Sterk; Alzbeta Krutosíková
Journal:  Molecules       Date:  2004-01-31       Impact factor: 4.411
  4 in total

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