Synthesis of New Cyano-Substituted bis-Benzothiazolyl Arylfurans and Arylthiophenes

The new compounds 2-[4-(6-cyanobenzothiazol-2-yl)phenyl]-5-(6-cyano- benzothiazol-2-yl)furan (6a) and 2-[4-(6-Cyanobenzothiazol-2-yl)phenyl]-5-(6-cyano- benzothiazol-2-yl)thiophene (6b) were synthesized by multi-step reactions from the corresponding 2-furan and 2-thiophene carboxaldehydes (route A),...

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Autores principales: Racanè, Livio, Tralić-Kulenović, Vesna, Boykin, David W., Karminski-Zamola, Grace
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2003
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6146956/
http://dx.doi.org/10.3390/80300342
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author Racanè, Livio
Tralić-Kulenović, Vesna
Boykin, David W.
Karminski-Zamola, Grace
author_facet Racanè, Livio
Tralić-Kulenović, Vesna
Boykin, David W.
Karminski-Zamola, Grace
author_sort Racanè, Livio
collection PubMed
description The new compounds 2-[4-(6-cyanobenzothiazol-2-yl)phenyl]-5-(6-cyano- benzothiazol-2-yl)furan (6a) and 2-[4-(6-Cyanobenzothiazol-2-yl)phenyl]-5-(6-cyano- benzothiazol-2-yl)thiophene (6b) were synthesized by multi-step reactions from the corresponding 2-furan and 2-thiophene carboxaldehydes (route A), as well as from 2- furan and 2- thiophene carboxylic acids (route B). Route B involves one less step than route A, but the overall yields of the reactions are considerably lower.
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spelling pubmed-61469562018-11-19 Synthesis of New Cyano-Substituted bis-Benzothiazolyl Arylfurans and Arylthiophenes Racanè, Livio Tralić-Kulenović, Vesna Boykin, David W. Karminski-Zamola, Grace Molecules Article The new compounds 2-[4-(6-cyanobenzothiazol-2-yl)phenyl]-5-(6-cyano- benzothiazol-2-yl)furan (6a) and 2-[4-(6-Cyanobenzothiazol-2-yl)phenyl]-5-(6-cyano- benzothiazol-2-yl)thiophene (6b) were synthesized by multi-step reactions from the corresponding 2-furan and 2-thiophene carboxaldehydes (route A), as well as from 2- furan and 2- thiophene carboxylic acids (route B). Route B involves one less step than route A, but the overall yields of the reactions are considerably lower. MDPI 2003-03-31 /pmc/articles/PMC6146956/ http://dx.doi.org/10.3390/80300342 Text en © 2003 by MDPI (http://www.mdpi.org). Reproduction is permitted for noncommercial purposes.
spellingShingle Article
Racanè, Livio
Tralić-Kulenović, Vesna
Boykin, David W.
Karminski-Zamola, Grace
Synthesis of New Cyano-Substituted bis-Benzothiazolyl Arylfurans and Arylthiophenes
title Synthesis of New Cyano-Substituted bis-Benzothiazolyl Arylfurans and Arylthiophenes
title_full Synthesis of New Cyano-Substituted bis-Benzothiazolyl Arylfurans and Arylthiophenes
title_fullStr Synthesis of New Cyano-Substituted bis-Benzothiazolyl Arylfurans and Arylthiophenes
title_full_unstemmed Synthesis of New Cyano-Substituted bis-Benzothiazolyl Arylfurans and Arylthiophenes
title_short Synthesis of New Cyano-Substituted bis-Benzothiazolyl Arylfurans and Arylthiophenes
title_sort synthesis of new cyano-substituted bis-benzothiazolyl arylfurans and arylthiophenes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6146956/
http://dx.doi.org/10.3390/80300342
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