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A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones
The acylation of the acetonitrile anion with lactones and esters in ethereal solvents was successfully exploited using inexpensive KOt-Bu to obtain a variety of β-ketonitriles and trifunctionalized building blocks, including useful O-unprotected diols. It was discovered that lactones react to produc...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902896/ https://www.ncbi.nlm.nih.gov/pubmed/31839839 http://dx.doi.org/10.3762/bjoc.15.287 |
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author | Pienaar, Daniel P Butsi, Kamogelo R Rousseau, Amanda L Brady, Dean |
author_facet | Pienaar, Daniel P Butsi, Kamogelo R Rousseau, Amanda L Brady, Dean |
author_sort | Pienaar, Daniel P |
collection | PubMed |
description | The acylation of the acetonitrile anion with lactones and esters in ethereal solvents was successfully exploited using inexpensive KOt-Bu to obtain a variety of β-ketonitriles and trifunctionalized building blocks, including useful O-unprotected diols. It was discovered that lactones react to produce the corresponding derivatized cyclic hemiketals. Furthermore, the addition of a catalytic amount of isopropanol, or 18-crown-6, was necessary to facilitate the reaction and to reduce side-product formation under ambient conditions. |
format | Online Article Text |
id | pubmed-6902896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-69028962019-12-13 A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones Pienaar, Daniel P Butsi, Kamogelo R Rousseau, Amanda L Brady, Dean Beilstein J Org Chem Letter The acylation of the acetonitrile anion with lactones and esters in ethereal solvents was successfully exploited using inexpensive KOt-Bu to obtain a variety of β-ketonitriles and trifunctionalized building blocks, including useful O-unprotected diols. It was discovered that lactones react to produce the corresponding derivatized cyclic hemiketals. Furthermore, the addition of a catalytic amount of isopropanol, or 18-crown-6, was necessary to facilitate the reaction and to reduce side-product formation under ambient conditions. Beilstein-Institut 2019-12-06 /pmc/articles/PMC6902896/ /pubmed/31839839 http://dx.doi.org/10.3762/bjoc.15.287 Text en Copyright © 2019, Pienaar et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Letter Pienaar, Daniel P Butsi, Kamogelo R Rousseau, Amanda L Brady, Dean A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones |
title | A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones |
title_full | A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones |
title_fullStr | A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones |
title_full_unstemmed | A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones |
title_short | A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones |
title_sort | green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902896/ https://www.ncbi.nlm.nih.gov/pubmed/31839839 http://dx.doi.org/10.3762/bjoc.15.287 |
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