A novel and efficient one-pot strategy for the synthesis of 1,2,4-triazoles: access to synthesis of penipanoid A and its analogues

We developed a novel one-pot strategy for synthesizing biologically important 1,2,4-triazole motifs from easily accessible 4-hydroxy phenylacetic acid, formamidine hydrochloride and hydrazine derivatives under mild conditions. This strategy enabled us to synthesize the natural penipanoid A and its a...

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Detalles Bibliográficos
Autores principales: Reddy, A. Satyanarayana, Reddy, V. Krishna, Rao, G. Nageswara, Basavaiah, K., Nagulapalli Venkata, Kalyan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9846445/
https://www.ncbi.nlm.nih.gov/pubmed/36741146
http://dx.doi.org/10.1039/d2ra06341g
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author Reddy, A. Satyanarayana
Reddy, V. Krishna
Rao, G. Nageswara
Basavaiah, K.
Nagulapalli Venkata, Kalyan C.
author_facet Reddy, A. Satyanarayana
Reddy, V. Krishna
Rao, G. Nageswara
Basavaiah, K.
Nagulapalli Venkata, Kalyan C.
author_sort Reddy, A. Satyanarayana
collection PubMed
description We developed a novel one-pot strategy for synthesizing biologically important 1,2,4-triazole motifs from easily accessible 4-hydroxy phenylacetic acid, formamidine hydrochloride and hydrazine derivatives under mild conditions. This strategy enabled us to synthesize the natural penipanoid A and its analogues in one step.
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spelling pubmed-98464452023-02-03 A novel and efficient one-pot strategy for the synthesis of 1,2,4-triazoles: access to synthesis of penipanoid A and its analogues Reddy, A. Satyanarayana Reddy, V. Krishna Rao, G. Nageswara Basavaiah, K. Nagulapalli Venkata, Kalyan C. RSC Adv Chemistry We developed a novel one-pot strategy for synthesizing biologically important 1,2,4-triazole motifs from easily accessible 4-hydroxy phenylacetic acid, formamidine hydrochloride and hydrazine derivatives under mild conditions. This strategy enabled us to synthesize the natural penipanoid A and its analogues in one step. The Royal Society of Chemistry 2023-01-18 /pmc/articles/PMC9846445/ /pubmed/36741146 http://dx.doi.org/10.1039/d2ra06341g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Reddy, A. Satyanarayana
Reddy, V. Krishna
Rao, G. Nageswara
Basavaiah, K.
Nagulapalli Venkata, Kalyan C.
A novel and efficient one-pot strategy for the synthesis of 1,2,4-triazoles: access to synthesis of penipanoid A and its analogues
title A novel and efficient one-pot strategy for the synthesis of 1,2,4-triazoles: access to synthesis of penipanoid A and its analogues
title_full A novel and efficient one-pot strategy for the synthesis of 1,2,4-triazoles: access to synthesis of penipanoid A and its analogues
title_fullStr A novel and efficient one-pot strategy for the synthesis of 1,2,4-triazoles: access to synthesis of penipanoid A and its analogues
title_full_unstemmed A novel and efficient one-pot strategy for the synthesis of 1,2,4-triazoles: access to synthesis of penipanoid A and its analogues
title_short A novel and efficient one-pot strategy for the synthesis of 1,2,4-triazoles: access to synthesis of penipanoid A and its analogues
title_sort novel and efficient one-pot strategy for the synthesis of 1,2,4-triazoles: access to synthesis of penipanoid a and its analogues
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9846445/
https://www.ncbi.nlm.nih.gov/pubmed/36741146
http://dx.doi.org/10.1039/d2ra06341g
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