Results 101 to 110 of about 1,302 (169)

Stereocontrolled synthesis of polyhydroxylated bicyclic azetidines as a new class of iminosugars

open access: yes, 2018
First examples of a new class of constrained bicyclic iminosugars have been synthesized by a non-classical Dieckmann-like reaction.
Nicolas Kern   +6 more
core   +1 more source

Total asymmetric syntheses of iminosugars

open access: yes, 2015
This thesis is concerned with the development of ring-closing iodoamination and ringexpansion methodology and its subsequent application to the asymmetric syntheses of pyrrolidine and piperidine iminosugars. Chapter 1 highlights the remarkable biological properties displayed by iminosugars and introduces methods for the formation of the pyrrolidine and
Figuccia, A, Figuccia, Aude
openaire   +1 more source

N-Alkylated L-Iminosugars as novel anti-inflammatory and anti-biofilm tools for Cystic Fibrosis Lung Infections

open access: yes, 2019
In search for novel drug targets aimed to control CF lung infections, a key role of the non-lysosomal glucosidase 2 (GBA2-encoded GNLase) in proinflammatory state characterizing CF cells has been highlighted.
Munari, S.   +16 more
core  

Synthesis of N-alkyl substituted iminosugars from D-ribose

open access: yes, 2017
An effective and facile method for the synthesis of N-alkylated hydroxylpyrrolidine and hydroxylpiperidine is described. A number of N-alkyl substituted iminosugars were prepared using iodine-induced intramolecular cyclization of acyclic alkenylamines as
Wei Zou   +9 more
core   +1 more source

Synthesis and biological properties of multivalent iminosugars

open access: yes, 2015
International audienceGlycosidases are extremely widespread enzymes responsible for the cleavage of glycosidic bonds in glycoconjugates found in living organisms.
Marra, Alberto   +3 more
core   +1 more source

A Rapid Synthesis of Hexofuranose-like Iminosugars Using Ring-Closing Metathesis

open access: yes, 2016
Two new 1-N-iminosugars have been prepared as hexofuranose analogues in an efficient manner by an RCM-based route. Both 3,4-disubstituted pyrrolidines display moderate inhibitory activity against Mycobacterium smegmatis galactan ...
Neil R. Thomas (1937950)   +2 more
core   +1 more source

Stereocontrolled synthesis of pyrrolidine iminosugars through asymmetric dihydroxylation of optically active olefins

open access: yes, 2018
Iminosugars, carbohydrate analogues in which the endocyclic oxygen is replaced by a nitrogen atom, are nowadays the most attractive class of sugar mimics because of their high glycosidase and glycosyltransferase inhibitor activity and hence their ...
Righi Giuliana   +5 more
core  

An Efficient and Simple Method for Stereoselective Synthesis of N-Substituted Iminosugars from D-Xylose Derivative

open access: yes, 2014
A series of new N-substituted iminosugars were successfully synthesized through a general synthetic route from D-xylose derivative. This approach provided a convenient access to the synthesis of N-alkylated iminosugars as potential glucosidase inhibitors,
Zhang, Jichao   +5 more
core  

Stereocontrolled synthesis of pyrrolidine iminosugars through asymmetric dihydroxylation reaction

open access: yes, 2019
Iminosugars are carbohydrate analogues in which the endocyclic oxygen is replaced by a nitrogen atom [1]. These compounds are nowadays the most attractive class of sugar mimics because of their high glycosidase and glycosyltransferase inhibitor activity ...
Forte, Giorgia   +5 more
core  

The synthesis of azetidine and piperidine iminosugars from monosaccharides

open access: yes, 2012
Iminosugars are polyhydroxylated alkaloids, and can be generally defined as sugar mimetics in which the endocyclic oxygen atom has been replaced with a basic nitrogen.
Fleet, George W J   +1 more
core  

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