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Synthesis and structure of tricarbonyl(η(6)-arene)chromium complexes of phenyl and benzyl D-glycopyranosides

A series of 15 glycoside-derived tricarbonyl(η(6)-arene)chromium complexes were prepared in 19–87% yield by heating fully acetylated or methylated aryl O-, S-, N- and C-glycosides of D-glucopyranose and D-mannopyranose with hexacarbonylchromium. All tricarbonylchromium complexes were fully character...

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Autores principales: Ziegler, Thomas, Heber, Ulrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458723/
https://www.ncbi.nlm.nih.gov/pubmed/23019433
http://dx.doi.org/10.3762/bjoc.8.118
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author Ziegler, Thomas
Heber, Ulrich
author_facet Ziegler, Thomas
Heber, Ulrich
author_sort Ziegler, Thomas
collection PubMed
description A series of 15 glycoside-derived tricarbonyl(η(6)-arene)chromium complexes were prepared in 19–87% yield by heating fully acetylated or methylated aryl O-, S-, N- and C-glycosides of D-glucopyranose and D-mannopyranose with hexacarbonylchromium. All tricarbonylchromium complexes were fully characterized. The structures of nine crystalline complexes were determined by X-ray diffraction, revealing unusual intra- and intermolecular nonclassical hydrogen bonds.
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spelling pubmed-34587232012-09-27 Synthesis and structure of tricarbonyl(η(6)-arene)chromium complexes of phenyl and benzyl D-glycopyranosides Ziegler, Thomas Heber, Ulrich Beilstein J Org Chem Full Research Paper A series of 15 glycoside-derived tricarbonyl(η(6)-arene)chromium complexes were prepared in 19–87% yield by heating fully acetylated or methylated aryl O-, S-, N- and C-glycosides of D-glucopyranose and D-mannopyranose with hexacarbonylchromium. All tricarbonylchromium complexes were fully characterized. The structures of nine crystalline complexes were determined by X-ray diffraction, revealing unusual intra- and intermolecular nonclassical hydrogen bonds. Beilstein-Institut 2012-07-11 /pmc/articles/PMC3458723/ /pubmed/23019433 http://dx.doi.org/10.3762/bjoc.8.118 Text en Copyright © 2012, Ziegler and Heber 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
Ziegler, Thomas
Heber, Ulrich
Synthesis and structure of tricarbonyl(η(6)-arene)chromium complexes of phenyl and benzyl D-glycopyranosides
title Synthesis and structure of tricarbonyl(η(6)-arene)chromium complexes of phenyl and benzyl D-glycopyranosides
title_full Synthesis and structure of tricarbonyl(η(6)-arene)chromium complexes of phenyl and benzyl D-glycopyranosides
title_fullStr Synthesis and structure of tricarbonyl(η(6)-arene)chromium complexes of phenyl and benzyl D-glycopyranosides
title_full_unstemmed Synthesis and structure of tricarbonyl(η(6)-arene)chromium complexes of phenyl and benzyl D-glycopyranosides
title_short Synthesis and structure of tricarbonyl(η(6)-arene)chromium complexes of phenyl and benzyl D-glycopyranosides
title_sort synthesis and structure of tricarbonyl(η(6)-arene)chromium complexes of phenyl and benzyl d-glycopyranosides
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458723/
https://www.ncbi.nlm.nih.gov/pubmed/23019433
http://dx.doi.org/10.3762/bjoc.8.118
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