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A Simple and Versatile Method for the Formation of Acetals/Ketals Using Trace Conventional Acids
[Image: see text] An important and surprising finding that the acetalization and ketalization of aldehydes and ketones with alcohols, respectively, proceed smoothly in the presence of 0.1 mol % acid, without removing water, has been presented. This process has many merits, such as commercial availab...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641695/ https://www.ncbi.nlm.nih.gov/pubmed/31458712 http://dx.doi.org/10.1021/acsomega.8b00159 |
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author | Dong, Jian-Lian Yu, Li-Si-Han Xie, Jian-Wu |
author_facet | Dong, Jian-Lian Yu, Li-Si-Han Xie, Jian-Wu |
author_sort | Dong, Jian-Lian |
collection | PubMed |
description | [Image: see text] An important and surprising finding that the acetalization and ketalization of aldehydes and ketones with alcohols, respectively, proceed smoothly in the presence of 0.1 mol % acid, without removing water, has been presented. This process has many merits, such as commercial available catalysts with low cost and low loadings (as low as 0.03 mol %), quite a broad substrate scope (including various aldehydes, ketones, acid-sensitive substrates, and diols), a wide range of reaction temperature (−60 to 50 °C), high yields, large-scale preparation, environmental friendliness, and simple work-up procedure. This new protocol has also been successfully applied to protect the important organic compounds, such as 1,3-diols, 1,2-diols, acid-sensitive substrates, glucose, and 1,3-dicarbonyl compounds. |
format | Online Article Text |
id | pubmed-6641695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66416952019-08-27 A Simple and Versatile Method for the Formation of Acetals/Ketals Using Trace Conventional Acids Dong, Jian-Lian Yu, Li-Si-Han Xie, Jian-Wu ACS Omega [Image: see text] An important and surprising finding that the acetalization and ketalization of aldehydes and ketones with alcohols, respectively, proceed smoothly in the presence of 0.1 mol % acid, without removing water, has been presented. This process has many merits, such as commercial available catalysts with low cost and low loadings (as low as 0.03 mol %), quite a broad substrate scope (including various aldehydes, ketones, acid-sensitive substrates, and diols), a wide range of reaction temperature (−60 to 50 °C), high yields, large-scale preparation, environmental friendliness, and simple work-up procedure. This new protocol has also been successfully applied to protect the important organic compounds, such as 1,3-diols, 1,2-diols, acid-sensitive substrates, glucose, and 1,3-dicarbonyl compounds. American Chemical Society 2018-05-07 /pmc/articles/PMC6641695/ /pubmed/31458712 http://dx.doi.org/10.1021/acsomega.8b00159 Text en Copyright © 2018 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 | Dong, Jian-Lian Yu, Li-Si-Han Xie, Jian-Wu A Simple and Versatile Method for the Formation of Acetals/Ketals Using Trace Conventional Acids |
title | A Simple and Versatile Method for the Formation of
Acetals/Ketals Using Trace Conventional Acids |
title_full | A Simple and Versatile Method for the Formation of
Acetals/Ketals Using Trace Conventional Acids |
title_fullStr | A Simple and Versatile Method for the Formation of
Acetals/Ketals Using Trace Conventional Acids |
title_full_unstemmed | A Simple and Versatile Method for the Formation of
Acetals/Ketals Using Trace Conventional Acids |
title_short | A Simple and Versatile Method for the Formation of
Acetals/Ketals Using Trace Conventional Acids |
title_sort | simple and versatile method for the formation of
acetals/ketals using trace conventional acids |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641695/ https://www.ncbi.nlm.nih.gov/pubmed/31458712 http://dx.doi.org/10.1021/acsomega.8b00159 |
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