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Cross-metathesis reaction of α- and β-vinyl C-glycosides with alkenes
Cross-metathesis of α- and β-vinyl C-deoxyribosides and α-vinyl C-galactoside with various terminal alkenes under different conditions was studied. The cross-metathesis of the former proceeded with good yields of the corresponding products in ClCH(2)CH(2)Cl the latter required the presence of CuI in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578437/ https://www.ncbi.nlm.nih.gov/pubmed/26425194 http://dx.doi.org/10.3762/bjoc.11.150 |
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author | Šnajdr, Ivan Parkan, Kamil Hessler, Filip Kotora, Martin |
author_facet | Šnajdr, Ivan Parkan, Kamil Hessler, Filip Kotora, Martin |
author_sort | Šnajdr, Ivan |
collection | PubMed |
description | Cross-metathesis of α- and β-vinyl C-deoxyribosides and α-vinyl C-galactoside with various terminal alkenes under different conditions was studied. The cross-metathesis of the former proceeded with good yields of the corresponding products in ClCH(2)CH(2)Cl the latter required the presence of CuI in CH(2)Cl(2) to achieve good yields of the products. A simple method for the preparation of α- and β-vinyl C-deoxyribosides was also developed. In addition, feasibility of deprotection and further transformations were briefly explored. |
format | Online Article Text |
id | pubmed-4578437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-45784372015-09-30 Cross-metathesis reaction of α- and β-vinyl C-glycosides with alkenes Šnajdr, Ivan Parkan, Kamil Hessler, Filip Kotora, Martin Beilstein J Org Chem Full Research Paper Cross-metathesis of α- and β-vinyl C-deoxyribosides and α-vinyl C-galactoside with various terminal alkenes under different conditions was studied. The cross-metathesis of the former proceeded with good yields of the corresponding products in ClCH(2)CH(2)Cl the latter required the presence of CuI in CH(2)Cl(2) to achieve good yields of the products. A simple method for the preparation of α- and β-vinyl C-deoxyribosides was also developed. In addition, feasibility of deprotection and further transformations were briefly explored. Beilstein-Institut 2015-08-10 /pmc/articles/PMC4578437/ /pubmed/26425194 http://dx.doi.org/10.3762/bjoc.11.150 Text en Copyright © 2015, Šnajdr 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 Šnajdr, Ivan Parkan, Kamil Hessler, Filip Kotora, Martin Cross-metathesis reaction of α- and β-vinyl C-glycosides with alkenes |
title | Cross-metathesis reaction of α- and β-vinyl C-glycosides with alkenes |
title_full | Cross-metathesis reaction of α- and β-vinyl C-glycosides with alkenes |
title_fullStr | Cross-metathesis reaction of α- and β-vinyl C-glycosides with alkenes |
title_full_unstemmed | Cross-metathesis reaction of α- and β-vinyl C-glycosides with alkenes |
title_short | Cross-metathesis reaction of α- and β-vinyl C-glycosides with alkenes |
title_sort | cross-metathesis reaction of α- and β-vinyl c-glycosides with alkenes |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578437/ https://www.ncbi.nlm.nih.gov/pubmed/26425194 http://dx.doi.org/10.3762/bjoc.11.150 |
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