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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...

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Detalles Bibliográficos
Autores principales: Talasila, Deva Saroja, Bauer, Eike B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
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).
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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
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