Dimerization of propargyl and homopropargyl 6-azido-6-deoxy-glycosides upon 1,3-dipolar cycloaddition

Copper-catalyzed, thermal or microwave promoted 1,3-dipolar cycloaddition (Click Reaction) of 2-propynyl and 3-butynyl 2,3,4-tri-O-acetyl-6-azido-6-deoxy-glycopyranosides in the D-gluco, D-galacto and D-manno series afford the corresponding dimeric cycloaddition products.

Detalles Bibliográficos
Autores principales: Pietrzik, Nikolas, Schmollinger, Daniel, Ziegler, Thomas
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2008
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2533435/
https://www.ncbi.nlm.nih.gov/pubmed/18941499
http://dx.doi.org/10.3762/bjoc.4.30
_version_ 1782159044029448192
author Pietrzik, Nikolas
Schmollinger, Daniel
Ziegler, Thomas
author_facet Pietrzik, Nikolas
Schmollinger, Daniel
Ziegler, Thomas
author_sort Pietrzik, Nikolas
collection PubMed
description Copper-catalyzed, thermal or microwave promoted 1,3-dipolar cycloaddition (Click Reaction) of 2-propynyl and 3-butynyl 2,3,4-tri-O-acetyl-6-azido-6-deoxy-glycopyranosides in the D-gluco, D-galacto and D-manno series afford the corresponding dimeric cycloaddition products.
format Text
id pubmed-2533435
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher Beilstein-Institut
record_format MEDLINE/PubMed
spelling pubmed-25334352008-10-20 Dimerization of propargyl and homopropargyl 6-azido-6-deoxy-glycosides upon 1,3-dipolar cycloaddition Pietrzik, Nikolas Schmollinger, Daniel Ziegler, Thomas Beilstein J Org Chem Full Research Paper Copper-catalyzed, thermal or microwave promoted 1,3-dipolar cycloaddition (Click Reaction) of 2-propynyl and 3-butynyl 2,3,4-tri-O-acetyl-6-azido-6-deoxy-glycopyranosides in the D-gluco, D-galacto and D-manno series afford the corresponding dimeric cycloaddition products. Beilstein-Institut 2008-08-13 /pmc/articles/PMC2533435/ /pubmed/18941499 http://dx.doi.org/10.3762/bjoc.4.30 Text en Copyright © 2008, Pietrzik 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
Pietrzik, Nikolas
Schmollinger, Daniel
Ziegler, Thomas
Dimerization of propargyl and homopropargyl 6-azido-6-deoxy-glycosides upon 1,3-dipolar cycloaddition
title Dimerization of propargyl and homopropargyl 6-azido-6-deoxy-glycosides upon 1,3-dipolar cycloaddition
title_full Dimerization of propargyl and homopropargyl 6-azido-6-deoxy-glycosides upon 1,3-dipolar cycloaddition
title_fullStr Dimerization of propargyl and homopropargyl 6-azido-6-deoxy-glycosides upon 1,3-dipolar cycloaddition
title_full_unstemmed Dimerization of propargyl and homopropargyl 6-azido-6-deoxy-glycosides upon 1,3-dipolar cycloaddition
title_short Dimerization of propargyl and homopropargyl 6-azido-6-deoxy-glycosides upon 1,3-dipolar cycloaddition
title_sort dimerization of propargyl and homopropargyl 6-azido-6-deoxy-glycosides upon 1,3-dipolar cycloaddition
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2533435/
https://www.ncbi.nlm.nih.gov/pubmed/18941499
http://dx.doi.org/10.3762/bjoc.4.30
work_keys_str_mv AT pietrziknikolas dimerizationofpropargylandhomopropargyl6azido6deoxyglycosidesupon13dipolarcycloaddition
AT schmollingerdaniel dimerizationofpropargylandhomopropargyl6azido6deoxyglycosidesupon13dipolarcycloaddition
AT zieglerthomas dimerizationofpropargylandhomopropargyl6azido6deoxyglycosidesupon13dipolarcycloaddition

Ejemplares similares