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Metal-free hypervalent iodine/TEMPO mediated oxidation of amines and mechanistic insight into the reaction pathways
A highly efficient metal free approach for the oxidation of primary and secondary amines to their corresponding aldehydes and ketones using PhI(OAc)(2) in combination with a catalytic amount of TEMPO as an oxidizing agent is described. This protocol is rapid and provides diverse products under milde...
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/PMC9086218/ https://www.ncbi.nlm.nih.gov/pubmed/35547530 http://dx.doi.org/10.1039/c8ra07451h |
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author | Bansode, Ajay H. Suryavanshi, Gurunath |
author_facet | Bansode, Ajay H. Suryavanshi, Gurunath |
author_sort | Bansode, Ajay H. |
collection | PubMed |
description | A highly efficient metal free approach for the oxidation of primary and secondary amines to their corresponding aldehydes and ketones using PhI(OAc)(2) in combination with a catalytic amount of TEMPO as an oxidizing agent is described. This protocol is rapid and provides diverse products under milder reaction conditions in excellent yields. In addition, the mechanistic study is well demonstrated by spectroscopic methods. |
format | Online Article Text |
id | pubmed-9086218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90862182022-05-10 Metal-free hypervalent iodine/TEMPO mediated oxidation of amines and mechanistic insight into the reaction pathways Bansode, Ajay H. Suryavanshi, Gurunath RSC Adv Chemistry A highly efficient metal free approach for the oxidation of primary and secondary amines to their corresponding aldehydes and ketones using PhI(OAc)(2) in combination with a catalytic amount of TEMPO as an oxidizing agent is described. This protocol is rapid and provides diverse products under milder reaction conditions in excellent yields. In addition, the mechanistic study is well demonstrated by spectroscopic methods. The Royal Society of Chemistry 2018-09-14 /pmc/articles/PMC9086218/ /pubmed/35547530 http://dx.doi.org/10.1039/c8ra07451h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Bansode, Ajay H. Suryavanshi, Gurunath Metal-free hypervalent iodine/TEMPO mediated oxidation of amines and mechanistic insight into the reaction pathways |
title | Metal-free hypervalent iodine/TEMPO mediated oxidation of amines and mechanistic insight into the reaction pathways |
title_full | Metal-free hypervalent iodine/TEMPO mediated oxidation of amines and mechanistic insight into the reaction pathways |
title_fullStr | Metal-free hypervalent iodine/TEMPO mediated oxidation of amines and mechanistic insight into the reaction pathways |
title_full_unstemmed | Metal-free hypervalent iodine/TEMPO mediated oxidation of amines and mechanistic insight into the reaction pathways |
title_short | Metal-free hypervalent iodine/TEMPO mediated oxidation of amines and mechanistic insight into the reaction pathways |
title_sort | metal-free hypervalent iodine/tempo mediated oxidation of amines and mechanistic insight into the reaction pathways |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086218/ https://www.ncbi.nlm.nih.gov/pubmed/35547530 http://dx.doi.org/10.1039/c8ra07451h |
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