153947-47-8Relevant articles and documents
Protecting group and solvent effects in electrochemical glycosylation
Drouin, Ludovic,Compton, Richard G.,Fietkau, Nicole,Fairbanks, Antony J.
, p. 2711 - 2717 (2008/02/13)
An investigation is undertaken into the roles of protecting groups and the solvent in the electrochemical-mediated glycosylation of manno thioglycosides. Herein notable differences are observed between electrochemical and chemical glycosylation. Georg Thi
Expedient stereospecific synthesis of β-mannosides from a glucose- derived 1,2-orthoester
Kaji, Eisuke,Hosokawa, Yugo
, p. 579 - 582 (2007/10/03)
A new, stereospecific synthesis of β-mannosides from glucose-derived 1,2-orthoester has been developed using a simple four-step procedure. For the synthesis of β-D-Man-(1→6)-D-Gal, a 6-OH free galactose derivative was glycosylated with the orthoester to yield β-D-Glc-(1→6)-D-Gal; the Glc unit of which was epimerized into the β-mannoside in good yield.
Route from Glycals to Mannose β-Glycosides
Liu, Kevin K.-C.,Danishefsky, Samuel J.
, p. 1892 - 1894 (2007/10/02)
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