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New Multi-1,2,3-Selenadiazole Aromatic Derivatives

The aromatic polyketones 3a-d are versatile compounds for the synthesis of the multi-1,2,3-selenadiazole aromatic derivatives 1a-d. The preparation starts with the reaction between the multi-bromomethylene benzene derivatives 2a-d and 4-hydroxy-acetophenone to give compounds 3a-d which are transform...

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Detalles Bibliográficos
Autores principales: Al-Smadi, Mousa, Ratrout, Samer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147698/
https://www.ncbi.nlm.nih.gov/pubmed/18007378
http://dx.doi.org/10.3390/10091126
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author Al-Smadi, Mousa
Ratrout, Samer
author_facet Al-Smadi, Mousa
Ratrout, Samer
author_sort Al-Smadi, Mousa
collection PubMed
description The aromatic polyketones 3a-d are versatile compounds for the synthesis of the multi-1,2,3-selenadiazole aromatic derivatives 1a-d. The preparation starts with the reaction between the multi-bromomethylene benzene derivatives 2a-d and 4-hydroxy-acetophenone to give compounds 3a-d which are transformed through the reaction with semicarbazide hydrochloride or ethyl hydrazine carboxylate into the corresponding semicarbazones derivatives 4a-d or hydrazones 5a-d. The reaction with selenium dioxide leads to regiospecific ring closure of semicarbazones or hydrazones to give the multi-1,2,3-selenadiazole aromatic derivatives in high yield.
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spelling pubmed-61476982018-11-19 New Multi-1,2,3-Selenadiazole Aromatic Derivatives Al-Smadi, Mousa Ratrout, Samer Molecules Article The aromatic polyketones 3a-d are versatile compounds for the synthesis of the multi-1,2,3-selenadiazole aromatic derivatives 1a-d. The preparation starts with the reaction between the multi-bromomethylene benzene derivatives 2a-d and 4-hydroxy-acetophenone to give compounds 3a-d which are transformed through the reaction with semicarbazide hydrochloride or ethyl hydrazine carboxylate into the corresponding semicarbazones derivatives 4a-d or hydrazones 5a-d. The reaction with selenium dioxide leads to regiospecific ring closure of semicarbazones or hydrazones to give the multi-1,2,3-selenadiazole aromatic derivatives in high yield. MDPI 2005-09-30 /pmc/articles/PMC6147698/ /pubmed/18007378 http://dx.doi.org/10.3390/10091126 Text en © 2005 by MDPI (http://www.mdpi.org). Reproduction is permitted for noncommercial purposes.
spellingShingle Article
Al-Smadi, Mousa
Ratrout, Samer
New Multi-1,2,3-Selenadiazole Aromatic Derivatives
title New Multi-1,2,3-Selenadiazole Aromatic Derivatives
title_full New Multi-1,2,3-Selenadiazole Aromatic Derivatives
title_fullStr New Multi-1,2,3-Selenadiazole Aromatic Derivatives
title_full_unstemmed New Multi-1,2,3-Selenadiazole Aromatic Derivatives
title_short New Multi-1,2,3-Selenadiazole Aromatic Derivatives
title_sort new multi-1,2,3-selenadiazole aromatic derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147698/
https://www.ncbi.nlm.nih.gov/pubmed/18007378
http://dx.doi.org/10.3390/10091126
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