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TfOH mediated intermolecular electrocyclization for the synthesis of pyrazolines and its application in alkaloid synthesis

TfOH mediated easy access to interesting pyrazolines starting from an aldehyde, phenylhydrazine and styrene has been developed. The scope of this synthetic methodology has been explored by synthesizing various 1,3,5-trisubstituted pyrazolines in very good yields with very high regioselectivity. The...

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Autores principales: Annes, Sesuraj Babiola, Vairaprakash, Pothiappan, Ramesh, Subburethinam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085413/
https://www.ncbi.nlm.nih.gov/pubmed/35546823
http://dx.doi.org/10.1039/c8ra05702h
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author Annes, Sesuraj Babiola
Vairaprakash, Pothiappan
Ramesh, Subburethinam
author_facet Annes, Sesuraj Babiola
Vairaprakash, Pothiappan
Ramesh, Subburethinam
author_sort Annes, Sesuraj Babiola
collection PubMed
description TfOH mediated easy access to interesting pyrazolines starting from an aldehyde, phenylhydrazine and styrene has been developed. The scope of this synthetic methodology has been explored by synthesizing various 1,3,5-trisubstituted pyrazolines in very good yields with very high regioselectivity. The origin of regioselectivity has been explained by comparing the stability of possible intermediate carbocations. The synthetic utility of a green solvent has been explored by synthesizing some of pyrazolines in a DES medium. The synthetic application of the present methodology is employed in the synthesis of a pyrazoline alkaloid.
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spelling pubmed-90854132022-05-10 TfOH mediated intermolecular electrocyclization for the synthesis of pyrazolines and its application in alkaloid synthesis Annes, Sesuraj Babiola Vairaprakash, Pothiappan Ramesh, Subburethinam RSC Adv Chemistry TfOH mediated easy access to interesting pyrazolines starting from an aldehyde, phenylhydrazine and styrene has been developed. The scope of this synthetic methodology has been explored by synthesizing various 1,3,5-trisubstituted pyrazolines in very good yields with very high regioselectivity. The origin of regioselectivity has been explained by comparing the stability of possible intermediate carbocations. The synthetic utility of a green solvent has been explored by synthesizing some of pyrazolines in a DES medium. The synthetic application of the present methodology is employed in the synthesis of a pyrazoline alkaloid. The Royal Society of Chemistry 2018-08-24 /pmc/articles/PMC9085413/ /pubmed/35546823 http://dx.doi.org/10.1039/c8ra05702h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Annes, Sesuraj Babiola
Vairaprakash, Pothiappan
Ramesh, Subburethinam
TfOH mediated intermolecular electrocyclization for the synthesis of pyrazolines and its application in alkaloid synthesis
title TfOH mediated intermolecular electrocyclization for the synthesis of pyrazolines and its application in alkaloid synthesis
title_full TfOH mediated intermolecular electrocyclization for the synthesis of pyrazolines and its application in alkaloid synthesis
title_fullStr TfOH mediated intermolecular electrocyclization for the synthesis of pyrazolines and its application in alkaloid synthesis
title_full_unstemmed TfOH mediated intermolecular electrocyclization for the synthesis of pyrazolines and its application in alkaloid synthesis
title_short TfOH mediated intermolecular electrocyclization for the synthesis of pyrazolines and its application in alkaloid synthesis
title_sort tfoh mediated intermolecular electrocyclization for the synthesis of pyrazolines and its application in alkaloid synthesis
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085413/
https://www.ncbi.nlm.nih.gov/pubmed/35546823
http://dx.doi.org/10.1039/c8ra05702h
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