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Aerobic Metal-Free Dioxygenation of Alkenes with tert-Butyl Nitrite and N-Hydroxylamines
[Image: see text] Metal-free dioxygenation of alkenes with tert-butyl nitrite and N-hydroxylamines (N-hydroxyphthalimide, N-hydroxybenzotriazole, and N-hydroxysuccinimide) is described to produce β-aminoxy nitrate esters using air as the oxidant. These organic nitrates can be readily converted into...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644589/ https://www.ncbi.nlm.nih.gov/pubmed/31457873 http://dx.doi.org/10.1021/acsomega.7b01111 |
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author | Bag, Raghunath Sar, Dinabandhu Punniyamurthy, Tharmalingam |
author_facet | Bag, Raghunath Sar, Dinabandhu Punniyamurthy, Tharmalingam |
author_sort | Bag, Raghunath |
collection | PubMed |
description | [Image: see text] Metal-free dioxygenation of alkenes with tert-butyl nitrite and N-hydroxylamines (N-hydroxyphthalimide, N-hydroxybenzotriazole, and N-hydroxysuccinimide) is described to produce β-aminoxy nitrate esters using air as the oxidant. These organic nitrates can be readily converted into 1,2-diols and 1,2-diketone with broad substrate scope and functional group diversity. |
format | Online Article Text |
id | pubmed-6644589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66445892019-08-27 Aerobic Metal-Free Dioxygenation of Alkenes with tert-Butyl Nitrite and N-Hydroxylamines Bag, Raghunath Sar, Dinabandhu Punniyamurthy, Tharmalingam ACS Omega [Image: see text] Metal-free dioxygenation of alkenes with tert-butyl nitrite and N-hydroxylamines (N-hydroxyphthalimide, N-hydroxybenzotriazole, and N-hydroxysuccinimide) is described to produce β-aminoxy nitrate esters using air as the oxidant. These organic nitrates can be readily converted into 1,2-diols and 1,2-diketone with broad substrate scope and functional group diversity. American Chemical Society 2017-09-29 /pmc/articles/PMC6644589/ /pubmed/31457873 http://dx.doi.org/10.1021/acsomega.7b01111 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Bag, Raghunath Sar, Dinabandhu Punniyamurthy, Tharmalingam Aerobic Metal-Free Dioxygenation of Alkenes with tert-Butyl Nitrite and N-Hydroxylamines |
title | Aerobic Metal-Free Dioxygenation of Alkenes with tert-Butyl Nitrite and N-Hydroxylamines |
title_full | Aerobic Metal-Free Dioxygenation of Alkenes with tert-Butyl Nitrite and N-Hydroxylamines |
title_fullStr | Aerobic Metal-Free Dioxygenation of Alkenes with tert-Butyl Nitrite and N-Hydroxylamines |
title_full_unstemmed | Aerobic Metal-Free Dioxygenation of Alkenes with tert-Butyl Nitrite and N-Hydroxylamines |
title_short | Aerobic Metal-Free Dioxygenation of Alkenes with tert-Butyl Nitrite and N-Hydroxylamines |
title_sort | aerobic metal-free dioxygenation of alkenes with tert-butyl nitrite and n-hydroxylamines |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644589/ https://www.ncbi.nlm.nih.gov/pubmed/31457873 http://dx.doi.org/10.1021/acsomega.7b01111 |
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