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Removal of benzylidene acetal and benzyl ether in carbohydrate derivatives using triethylsilane and Pd/C
Clean deprotection of carbohydrate derivatives containing benzylidene acetals and benzyl ethers was achieved under catalytic transfer hydrogenation conditions by using a combination of triethylsilane and 10% Pd/C in CH(3)OH at room temperature. A variety of carbohydrate diol derivatives were prepare...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566760/ https://www.ncbi.nlm.nih.gov/pubmed/23400301 http://dx.doi.org/10.3762/bjoc.9.9 |
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author | Santra, Abhishek Ghosh, Tamashree Misra, Anup Kumar |
author_facet | Santra, Abhishek Ghosh, Tamashree Misra, Anup Kumar |
author_sort | Santra, Abhishek |
collection | PubMed |
description | Clean deprotection of carbohydrate derivatives containing benzylidene acetals and benzyl ethers was achieved under catalytic transfer hydrogenation conditions by using a combination of triethylsilane and 10% Pd/C in CH(3)OH at room temperature. A variety of carbohydrate diol derivatives were prepared from their benzylidene derivatives in excellent yield. |
format | Online Article Text |
id | pubmed-3566760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-35667602013-02-11 Removal of benzylidene acetal and benzyl ether in carbohydrate derivatives using triethylsilane and Pd/C Santra, Abhishek Ghosh, Tamashree Misra, Anup Kumar Beilstein J Org Chem Full Research Paper Clean deprotection of carbohydrate derivatives containing benzylidene acetals and benzyl ethers was achieved under catalytic transfer hydrogenation conditions by using a combination of triethylsilane and 10% Pd/C in CH(3)OH at room temperature. A variety of carbohydrate diol derivatives were prepared from their benzylidene derivatives in excellent yield. Beilstein-Institut 2013-01-14 /pmc/articles/PMC3566760/ /pubmed/23400301 http://dx.doi.org/10.3762/bjoc.9.9 Text en Copyright © 2013, Santra et al. https://creativecommons.org/licenses/by/2.0https://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/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Santra, Abhishek Ghosh, Tamashree Misra, Anup Kumar Removal of benzylidene acetal and benzyl ether in carbohydrate derivatives using triethylsilane and Pd/C |
title | Removal of benzylidene acetal and benzyl ether in carbohydrate derivatives using triethylsilane and Pd/C |
title_full | Removal of benzylidene acetal and benzyl ether in carbohydrate derivatives using triethylsilane and Pd/C |
title_fullStr | Removal of benzylidene acetal and benzyl ether in carbohydrate derivatives using triethylsilane and Pd/C |
title_full_unstemmed | Removal of benzylidene acetal and benzyl ether in carbohydrate derivatives using triethylsilane and Pd/C |
title_short | Removal of benzylidene acetal and benzyl ether in carbohydrate derivatives using triethylsilane and Pd/C |
title_sort | removal of benzylidene acetal and benzyl ether in carbohydrate derivatives using triethylsilane and pd/c |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566760/ https://www.ncbi.nlm.nih.gov/pubmed/23400301 http://dx.doi.org/10.3762/bjoc.9.9 |
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