A versatile stereocontrolled synthesis of 2-deoxyiminosugar C-glycosides and their evaluation as glycosidase inhibitors

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Název: A versatile stereocontrolled synthesis of 2-deoxyiminosugar C-glycosides and their evaluation as glycosidase inhibitors
Autoři: Alexandre Lumbroso, Clément Berthonneau, Isabelle Beaudet, Jean-Paul Quintard, Aurélien Planchat, M. Isabel García-Moreno, Carmen Ortiz Mellet, Erwan Le Grognec
Přispěvatelé: Universidad de Sevilla. Departamento de Química orgánica, Institut de Chimie des Substances Naturelles (ICSN). France, Ministère de l'Enseignement Supérieur, de la Recherche et de l’Innovation (MESRI). France, Université de Rennes. France, Ministerio de Ciencia e Innovación (MICIN). España, Agencia Estatal de Investigación. España, European Commission (EC). Fondo Europeo de Desarrollo Regional (FEDER), Catalysis, ORganometallic chemistry And synthesIs of Ligands ( CORAIL), Chimie Et Interdisciplinarité : Synthèse, Analyse, Modélisation (CEISAM), Université de Nantes - UFR des Sciences et des Techniques (UN UFR ST), Université de Nantes (UN)-Université de Nantes (UN)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université de Nantes - UFR des Sciences et des Techniques (UN UFR ST), Université de Nantes (UN)-Université de Nantes (UN)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)
Zdroj: idUS. Depósito de Investigación de la Universidad de Sevilla
Universidad de Sevilla (US)
Informace o vydavateli: Royal Society of Chemistry (RSC), 2021.
Rok vydání: 2021
Témata: Models, Molecular, Molecular Stereoisomerism, Glycoside Hydrolases, Stereoisomerism, Chemistry Techniques, Synthetic, MESH: Carbohydrate Conformation Chemistry Techniques, 01 natural sciences, Imino Sugars, 3. Good health, 0104 chemical sciences, Synthetic Enzyme Inhibitors / chemical synthesis* Enzyme Inhibitors / chemistry Enzyme Inhibitors / pharmacology* Glycoside Hydrolases / antagonists & inhibitors* Glycosides / chemical synthesis* Glycosides / chemistry Glycosides / pharmacology* Imino Sugars / chemistry* Models, C-glycoside, 13. Climate action, Carbohydrate Conformation, [CHIM]Chemical Sciences, Glycosides, Enzyme Inhibitors
Popis: Dihydroxylation of (R,S) or (S,S)-2,6-disubstituted dehydropiperidines enantioselectively obtained from stannylated precursors allows a versatile preparation of 2-deoxyiminosugar C-glycosides which have been evaluated as glycosidases inhibitors.
Druh dokumentu: Article
Popis souboru: application/pdf
Jazyk: English
ISSN: 1477-0539
1477-0520
DOI: 10.1039/d0ob02249g
Přístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/33427829
https://hdl.handle.net/11441/141423
https://hal.archives-ouvertes.fr/hal-03376475
http://pubs.rsc.org/en/content/articlelanding/2021/ob/d0ob02249g
http://www.ncbi.nlm.nih.gov/pubmed/33427829
https://crystallography.net/cod/7157828.html
https://pubs.rsc.org/en/content/articlelanding/2021/ob/d0ob02249g
https://www.ncbi.nlm.nih.gov/pubmed/33427829
https://idus.us.es/handle//11441/141423
Rights: Royal Society of Chemistry Licence to Publish
CC BY NC ND
Přístupové číslo: edsair.doi.dedup.....81f7d08bfb233a3d16e4bf48692fb1e3
Databáze: OpenAIRE
Popis
Abstrakt:Dihydroxylation of (R,S) or (S,S)-2,6-disubstituted dehydropiperidines enantioselectively obtained from stannylated precursors allows a versatile preparation of 2-deoxyiminosugar C-glycosides which have been evaluated as glycosidases inhibitors.
ISSN:14770539
14770520
DOI:10.1039/d0ob02249g