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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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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. |
format | Online Article Text |
id | pubmed-9085413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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