Sugar 2,3-diphenyl-2-cyclopropen-l-yl ethers and their glycosylation. A new route to oligosaccharides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference7 articles.
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1. Efficient stereocontrolled synthesis of C-glycosides using glycosyl donors substituted by propane 1,3-diyl phosphate as the leaving group;Tetrahedron: Asymmetry;2001-07
2. The Synthesis of Blood Group I and i Active Oligosaccharides;Stereoselective Synthesis;1992
3. Synthesis of paragloboside analogs;Tetrahedron Letters;1978-01
4. Synthesis of a branched tetrasaccharide-2-acetamido-4-o-?-d-galactopyranosyl-6-o-[o-?-galactopyranosyl-(l?4)-?-d-glucopyranosyl]-2-desoxy-d-glucose;Bulletin of the Academy of Sciences of the USSR Division of Chemical Science;1976-06
5. Une synthése du 2-acètamido-2-désoxy-4-O-β-d-galactopyranosyl-α-d-glucopyranose (N-acétyllactosamine);Carbohydrate Research;1976-01
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