Carbohydrate Research p. 231 - 244 (1982)
Update date:2022-08-05
Topics: Regioselectivity Column chromatography NMR spectroscopy Thin-layer chromatography (TLC) Recrystallization Catalytic hydrogenation Mass spectrometry (MS) High-performance liquid chromatography (HPLC) Protecting group Anhydrous conditions Glycosylation Stereoselectivity Glycosyl acceptor Anomeric carbon Glycosyl donor
Abbas, Saled A.
Barlow, Joseph J.
Matta, Khushi L.
Glycosylation (catalyzed by mercuric cyanide) of p-nitrophenyl 2,4,6,-tri-O-acetyl-β-D-galactopyranoside (2) with 2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl bromide in acetonitrile afforded the α-(1->3)- and β-(1->3)-linked disaccharide heptaacetates (4
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(2019)Doi:10.1021/ja01117a047
(1953)Doi:10.1021/ol800576w
(2008)Doi:10.1016/j.ejmech.2009.10.034
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