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Me(3)SI-promoted chemoselective deacetylation: a general and mild protocol
A Me(3)SI-mediated simple and efficient protocol for the chemoselective deprotection of acetyl groups has been developed via employing KMnO(4) as an additive. This chemoselective deacetylation is amenable to a wide range of substrates, tolerating diverse and sensitive functional groups in carbohydra...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033574/ https://www.ncbi.nlm.nih.gov/pubmed/35478635 http://dx.doi.org/10.1039/d1ra03209g |
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author | Gurawa, Aakanksha Kumar, Manoj Kashyap, Sudhir |
author_facet | Gurawa, Aakanksha Kumar, Manoj Kashyap, Sudhir |
author_sort | Gurawa, Aakanksha |
collection | PubMed |
description | A Me(3)SI-mediated simple and efficient protocol for the chemoselective deprotection of acetyl groups has been developed via employing KMnO(4) as an additive. This chemoselective deacetylation is amenable to a wide range of substrates, tolerating diverse and sensitive functional groups in carbohydrates, amino acids, natural products, heterocycles, and general scaffolds. The protocol is attractive because it uses an environmentally benign reagent system to perform quantitative and clean transformations under ambient conditions. |
format | Online Article Text |
id | pubmed-9033574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90335742022-04-26 Me(3)SI-promoted chemoselective deacetylation: a general and mild protocol Gurawa, Aakanksha Kumar, Manoj Kashyap, Sudhir RSC Adv Chemistry A Me(3)SI-mediated simple and efficient protocol for the chemoselective deprotection of acetyl groups has been developed via employing KMnO(4) as an additive. This chemoselective deacetylation is amenable to a wide range of substrates, tolerating diverse and sensitive functional groups in carbohydrates, amino acids, natural products, heterocycles, and general scaffolds. The protocol is attractive because it uses an environmentally benign reagent system to perform quantitative and clean transformations under ambient conditions. The Royal Society of Chemistry 2021-05-27 /pmc/articles/PMC9033574/ /pubmed/35478635 http://dx.doi.org/10.1039/d1ra03209g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Gurawa, Aakanksha Kumar, Manoj Kashyap, Sudhir Me(3)SI-promoted chemoselective deacetylation: a general and mild protocol |
title | Me(3)SI-promoted chemoselective deacetylation: a general and mild protocol |
title_full | Me(3)SI-promoted chemoselective deacetylation: a general and mild protocol |
title_fullStr | Me(3)SI-promoted chemoselective deacetylation: a general and mild protocol |
title_full_unstemmed | Me(3)SI-promoted chemoselective deacetylation: a general and mild protocol |
title_short | Me(3)SI-promoted chemoselective deacetylation: a general and mild protocol |
title_sort | me(3)si-promoted chemoselective deacetylation: a general and mild protocol |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033574/ https://www.ncbi.nlm.nih.gov/pubmed/35478635 http://dx.doi.org/10.1039/d1ra03209g |
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