117253-42-6Relevant articles and documents
Novel selectivity in carbohydrate reactions III. selective deprotection of p-methoxybenzyl (PMBn) ethers of carbohydrates by tin(IV)chloride
Kartha, K.P. Ravindranathan,Kiso, Makoto,Hasegawa, Akira,Jennings
, p. 811 - 817 (1998)
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Synthesis of Double-Chain Bis-sulfone Neoglycolipids of the 2'-, 3'-, and 6'-Deoxyglobotrioses
Zhang, Zhiyuan,Magnusson, Goeran
, p. 7304 - 7315 (2007/10/03)
Partially protected 2-(trimethylsilyl)ethyl deoxylactosides (deoxygenated in the 2-, 3-, and 6-positions of the galactose unit) were synthesized via various routes and glycosylated with galactosyl donors to give the corresponding deoxytrisaccharides.Removal of the protecting groups gave the 2-(trimethylsilyl)ethyl 2'-, 3'-, and 6'-deoxyglobotriosides.Transformation of the protected trisaccharides into trichloroacetimidates, via the corresponding hemiacetals, proceeded in 86 - 96percent overall yield.Glycosylation of 3-(hexadecylsulfonyl)-2-propanol with the trisaccharidic trichloroacetimidates, in 37 - 68percent yield, followed by removal of protecting groups, gave the title neoglycolipids.