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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...

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Autores principales: Šnajdr, Ivan, Parkan, Kamil, Hessler, Filip, Kotora, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
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.
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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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