On May 17, 2019, Yalamanchili, Subbarao; Lloyd, Dina; Bennett, Clay S. published an article.Related Products of 2873-29-2 The title of the article was Synthesis of the Hexasaccharide Fragment of Landomycin A Using a Mild, Reagent-Controlled Approach. And the article contained the following:
The synthesis of the hexasaccharide fragment of landomycin A is reported. Using p-toluenesulfonyl chloride mediated dehydrative glycosylation, we constructed the deoxy-sugar linkages in a stereoselective fashion without the need for temporary prosthetic groups to control selectivity. Through this approach, the hexasaccharide was obtained in 28 steps and 8.9% overall yield, which is an order of magnitude higher than that of previously reported approaches. The experimental process involved the reaction of (2R,3S,4R)-2-(Acetoxymethyl)-3,4-dihydro-2H-pyran-3,4-diyl diacetate(cas: 2873-29-2).Related Products of 2873-29-2
The Article related to catalyst stereoselective dehydrative glycosylation toluenesulfonyl chloride, landomycin hexasaccharide synthesis synthon stereoselective glycosylation toluenesulfonyl chloride oligosaccharide and other aspects.Related Products of 2873-29-2
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