Titre de série :	Topics in Current Chemistry
Titre :	Vol.301 :Reactivity tuning in oligosaccharide assembly
Type de document :	texte imprimé
Auteurs :	B. Fraser-Reid, Éditeur scientifique ; J.C. Lopez, Éditeur scientifique
Editeur :	Berlin, Heidelberg : Springer
Année de publication :	2011
Collection :	Topics in Current Chemistry, ISSN 0340-1022 num. 301
Importance :	295 p
Présentation :	ill., couv. ill. en coul.
Format :	24 cm
ISBN/ISSN/EAN :	978-3-642-20913-0
Langues :	Anglais (eng)
Note de contenu :	"* Armed–disarmed effects in carbohydrate chemistry: History,synthetic and mechanistic studies * A survey of Ley’s reactivity tuning in oligosaccharide synthesis * “Active–latent” thioglycosyl donors and acceptors in oligosaccharide syntheses * Effect of electron-withdrawing protecting groups at remote positions of donors on glycosylation stereochemistry * Influence of protecting groups on the reactivity and selectivity of glycosylation: Chemistry of the 4,6-o-benzylidene protected mannopyranosyl donors and related species * Superarmed and Superdisarmed Building Blocks in Expeditious Oligosaccharide Synthesis * Programmable one-pot glycosylation * Uronic acids in oligosaccharide and glycoconjugate synthesis."
Cote :	EXCLU (SdL)
Num_Inv :	3041

Topics in Current Chemistry. Vol.301 :Reactivity tuning in oligosaccharide assembly [texte imprimé] / B. Fraser-Reid, Éditeur scientifique ; J.C. Lopez, Éditeur scientifique . - Berlin, Heidelberg : Springer, 2011 . - 295 p : ill., couv. ill. en coul. ; 24 cm. - (Topics in Current Chemistry, ISSN 0340-1022; 301) .
ISBN : 978-3-642-20913-0
Langues : Anglais (eng)

Note de contenu :	"* Armed–disarmed effects in carbohydrate chemistry: History,synthetic and mechanistic studies * A survey of Ley’s reactivity tuning in oligosaccharide synthesis * “Active–latent” thioglycosyl donors and acceptors in oligosaccharide syntheses * Effect of electron-withdrawing protecting groups at remote positions of donors on glycosylation stereochemistry * Influence of protecting groups on the reactivity and selectivity of glycosylation: Chemistry of the 4,6-o-benzylidene protected mannopyranosyl donors and related species * Superarmed and Superdisarmed Building Blocks in Expeditious Oligosaccharide Synthesis * Programmable one-pot glycosylation * Uronic acids in oligosaccharide and glycoconjugate synthesis."
Cote :	EXCLU (SdL)
Num_Inv :	3041