I(2)/DMSO-catalyzed one-pot approach for the synthesis of 1,3,4-selenadiazoles

A three-component cascade reaction for the synthesis of 1,3,4-selenadiazoles and their derivatives from arylaldehydes, hydrazine, and elemental selenium by using molecular iodine is reported. This strategy is operationally simple, well-suited to a wide range of functional groups, and provides the de...

Descripción completa

Detalles Bibliográficos
Autores principales: Bowroju, Suresh Kuarm, Bavanthula, Rajitha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694770/
https://www.ncbi.nlm.nih.gov/pubmed/35423114
http://dx.doi.org/10.1039/d0ra10576g
_version_ 1784619430537330688
author Bowroju, Suresh Kuarm
Bavanthula, Rajitha
author_facet Bowroju, Suresh Kuarm
Bavanthula, Rajitha
author_sort Bowroju, Suresh Kuarm
collection PubMed
description A three-component cascade reaction for the synthesis of 1,3,4-selenadiazoles and their derivatives from arylaldehydes, hydrazine, and elemental selenium by using molecular iodine is reported. This strategy is operationally simple, well-suited to a wide range of functional groups, and provides the desired products in moderate to excellent yields. The proposed mechanism predicts that the reaction tolerated a radical process.
format Online
Article
Text
id pubmed-8694770
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-86947702022-04-13 I(2)/DMSO-catalyzed one-pot approach for the synthesis of 1,3,4-selenadiazoles Bowroju, Suresh Kuarm Bavanthula, Rajitha RSC Adv Chemistry A three-component cascade reaction for the synthesis of 1,3,4-selenadiazoles and their derivatives from arylaldehydes, hydrazine, and elemental selenium by using molecular iodine is reported. This strategy is operationally simple, well-suited to a wide range of functional groups, and provides the desired products in moderate to excellent yields. The proposed mechanism predicts that the reaction tolerated a radical process. The Royal Society of Chemistry 2021-02-02 /pmc/articles/PMC8694770/ /pubmed/35423114 http://dx.doi.org/10.1039/d0ra10576g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Bowroju, Suresh Kuarm
Bavanthula, Rajitha
I(2)/DMSO-catalyzed one-pot approach for the synthesis of 1,3,4-selenadiazoles
title I(2)/DMSO-catalyzed one-pot approach for the synthesis of 1,3,4-selenadiazoles
title_full I(2)/DMSO-catalyzed one-pot approach for the synthesis of 1,3,4-selenadiazoles
title_fullStr I(2)/DMSO-catalyzed one-pot approach for the synthesis of 1,3,4-selenadiazoles
title_full_unstemmed I(2)/DMSO-catalyzed one-pot approach for the synthesis of 1,3,4-selenadiazoles
title_short I(2)/DMSO-catalyzed one-pot approach for the synthesis of 1,3,4-selenadiazoles
title_sort i(2)/dmso-catalyzed one-pot approach for the synthesis of 1,3,4-selenadiazoles
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694770/
https://www.ncbi.nlm.nih.gov/pubmed/35423114
http://dx.doi.org/10.1039/d0ra10576g
work_keys_str_mv AT bowrojusureshkuarm i2dmsocatalyzedonepotapproachforthesynthesisof134selenadiazoles
AT bavanthularajitha i2dmsocatalyzedonepotapproachforthesynthesisof134selenadiazoles

Ejemplares similares