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Ferrocenium complex aided O-glycosylation of glycosyl halides
A new strategy for the activation of glycosyl halide donors to be utilized in glycosylation reactions is presented, utilizing the ferrocenium (Fc) complexes [FcB(OH)(2)]SbF(6) and FcBF(4) as promoters. The scope of the new system has been investigated using glycosyl chloride and glycosyl fluoride do...
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/PMC9043573/ https://www.ncbi.nlm.nih.gov/pubmed/35494397 http://dx.doi.org/10.1039/d1ra05788j |
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author | Talasila, Deva Saroja Bauer, Eike B. |
author_facet | Talasila, Deva Saroja Bauer, Eike B. |
author_sort | Talasila, Deva Saroja |
collection | PubMed |
description | A new strategy for the activation of glycosyl halide donors to be utilized in glycosylation reactions is presented, utilizing the ferrocenium (Fc) complexes [FcB(OH)(2)]SbF(6) and FcBF(4) as promoters. The scope of the new system has been investigated using glycosyl chloride and glycosyl fluoride donors in combination with common glycosyl acceptors, such as protected glucose. The corresponding glycosylation products were formed in 95 to 10% isolated yields with α/β ratios ranging from 1/1 to β only (2 to 14 h reaction time at room temperature, 40 to 100% ferrocenium promoter load). |
format | Online Article Text |
id | pubmed-9043573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90435732022-04-28 Ferrocenium complex aided O-glycosylation of glycosyl halides Talasila, Deva Saroja Bauer, Eike B. RSC Adv Chemistry A new strategy for the activation of glycosyl halide donors to be utilized in glycosylation reactions is presented, utilizing the ferrocenium (Fc) complexes [FcB(OH)(2)]SbF(6) and FcBF(4) as promoters. The scope of the new system has been investigated using glycosyl chloride and glycosyl fluoride donors in combination with common glycosyl acceptors, such as protected glucose. The corresponding glycosylation products were formed in 95 to 10% isolated yields with α/β ratios ranging from 1/1 to β only (2 to 14 h reaction time at room temperature, 40 to 100% ferrocenium promoter load). The Royal Society of Chemistry 2021-11-17 /pmc/articles/PMC9043573/ /pubmed/35494397 http://dx.doi.org/10.1039/d1ra05788j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Talasila, Deva Saroja Bauer, Eike B. Ferrocenium complex aided O-glycosylation of glycosyl halides |
title | Ferrocenium complex aided O-glycosylation of glycosyl halides |
title_full | Ferrocenium complex aided O-glycosylation of glycosyl halides |
title_fullStr | Ferrocenium complex aided O-glycosylation of glycosyl halides |
title_full_unstemmed | Ferrocenium complex aided O-glycosylation of glycosyl halides |
title_short | Ferrocenium complex aided O-glycosylation of glycosyl halides |
title_sort | ferrocenium complex aided o-glycosylation of glycosyl halides |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043573/ https://www.ncbi.nlm.nih.gov/pubmed/35494397 http://dx.doi.org/10.1039/d1ra05788j |
work_keys_str_mv | AT talasiladevasaroja ferroceniumcomplexaidedoglycosylationofglycosylhalides AT bauereikeb ferroceniumcomplexaidedoglycosylationofglycosylhalides |