About: Simple Glycosylation Reaction of Allyl Glycosides

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_15/w
Subject	Note
Title	Simple Glycosylation Reaction of Allyl Glycosides
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_15/101021jo070512x/m/web http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_15/101021jo070512x/m/print
related by	http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_15/101021jo070512x/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_15/101021jo070512x/authorship/3 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_15/101021jo070512x/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_15/101021jo070512x/authorship/4
Author	Wang Pengfei Wang Yun Haldar Pranab Hu, Hongxia
Abstract	A simple glycosylation strategy employing only allyl glycosides is described. In a one-pot fashion, an allyl glycosideis first isomerized to the reactive 1-prop-en-yl glycosideintermediate, which subsequently undergoes glycosylationwith a glycosyl acceptor, promoted by NIS at room temperature.
article type	brief-report
is part of this journal	The Journal of Organic Chemistry

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