A method for the synthesis of a new family of 1-deoxy S-disaccharides has been established via free-radical hydrothiolation of glycals by sugar thiols (thiol-ene coupling). The photoinduced coupling between four tri-O-acetyl-D-glycals and three different sugar thiols reveals that the reaction efficiency and stereoselectivity are highly dependent on the stereochemistry of the OAc groups at C3 and C4 of the glycal. (C) 2011 Elsevier Ltd. All rights reserved
(Figure presented) Double glycosylation of cysteine-containing peptides has been carried out by a on...
Glycosyl thiols are widely used in stereoselective S-glycoside synthesis. Their epimerization from 1...
(Figure presented) Double glycosylation of cysteine-containing peptides has been carried out by a on...
A method for the synthesis of a new family of 1-deoxy S-disaccharides has been established via free ...
Free-radical hydrothiolation of the endocyclic double bond of enoses is reported. Reaction between 2...
Free-radical hydrothiolation of the endocyclic double bond of enoses is reported. Reaction between 2...
The high efficiency and selectivity of the thiol-ene radical reaction has been validated by the phot...
Oligosaccharides and glycoconjugates are abundant in all living organisms, taking part in a multitu...
Here, we present the synthesis of α-D-galactopyranosyl and α-L-fucopyranosyl thiodisaccharides 5-8 b...
Here, we present the synthesis of α-D-galactopyranosyl and α-L-fucopyranosyl thiodisaccharides 5-8 b...
We report on the photoinduced addition of glycosyl thiols to alkenyl glycines (thiol-ene coupling) t...
International audienceA study was performed for the coupling of thiols, thio-sugars, and thiol-conta...
Hydrofunctionalization of terminal double or triple bonds have become classical ligation tools for f...
A glycosyl coupling reaction via photoinduced direct activation of thioglycosides and subsequent O-g...
Free-radical hydrothiolation of O-peracylated 1-C-(carbamoyl-, methoxycarbonyl- and cyano) substitut...
(Figure presented) Double glycosylation of cysteine-containing peptides has been carried out by a on...
Glycosyl thiols are widely used in stereoselective S-glycoside synthesis. Their epimerization from 1...
(Figure presented) Double glycosylation of cysteine-containing peptides has been carried out by a on...
A method for the synthesis of a new family of 1-deoxy S-disaccharides has been established via free ...
Free-radical hydrothiolation of the endocyclic double bond of enoses is reported. Reaction between 2...
Free-radical hydrothiolation of the endocyclic double bond of enoses is reported. Reaction between 2...
The high efficiency and selectivity of the thiol-ene radical reaction has been validated by the phot...
Oligosaccharides and glycoconjugates are abundant in all living organisms, taking part in a multitu...
Here, we present the synthesis of α-D-galactopyranosyl and α-L-fucopyranosyl thiodisaccharides 5-8 b...
Here, we present the synthesis of α-D-galactopyranosyl and α-L-fucopyranosyl thiodisaccharides 5-8 b...
We report on the photoinduced addition of glycosyl thiols to alkenyl glycines (thiol-ene coupling) t...
International audienceA study was performed for the coupling of thiols, thio-sugars, and thiol-conta...
Hydrofunctionalization of terminal double or triple bonds have become classical ligation tools for f...
A glycosyl coupling reaction via photoinduced direct activation of thioglycosides and subsequent O-g...
Free-radical hydrothiolation of O-peracylated 1-C-(carbamoyl-, methoxycarbonyl- and cyano) substitut...
(Figure presented) Double glycosylation of cysteine-containing peptides has been carried out by a on...
Glycosyl thiols are widely used in stereoselective S-glycoside synthesis. Their epimerization from 1...
(Figure presented) Double glycosylation of cysteine-containing peptides has been carried out by a on...