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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2005
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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. |
format | Online Article Text |
id | pubmed-6147698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT alsmadimousa newmulti123selenadiazolearomaticderivatives AT ratroutsamer newmulti123selenadiazolearomaticderivatives |