506410-38-4

Upstream product

• 181489-22-5 3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propan-1-ol 

Downstream Products

• 506410-40-8 (R)-4-benzyl-3-[(R)-2-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosylmethyl)pent-4-enoyl]oxazolidin-2-one 
• 506410-42-0 (R)-4-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosylmethyl)-5-iodopent-1-ene 
• 506410-41-9 (R)-2-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosylmethyl)pent-4-en-1-ol 
• 506410-43-1 (R)-4-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosylmethyl)pent-1-ene 
• 881015-91-4 (Z)-(S)-2-Benzyloxycarbonylamino-5-(tert-butyl-dimethyl-silanyloxymethyl)-6-((2S,3S,4R,5S,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-hex-2-enoic acid methyl ester 
• 881015-92-5 (Z)-(S)-2-Benzyloxycarbonylamino-5-hydroxymethyl-6-((2S,3S,4R,5S,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-hex-2-enoic acid methyl ester 
• 881015-87-8 (4S)-4-benzyl-3-[(2S)-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosylmethyl)pent-4-enoyl]oxazolidin-2-one 
• 881015-86-7 (4S)-4-benzyl-3-[3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propionyl]oxazolidin-2-one 
• 881015-90-3 (3R)-3-(tert-butyldimethylsilanyloxymethyl)-4-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)butyraldehyde 
• 881015-89-0 (2S)-(tert-butyldimethylsilanyloxymethyl)-1-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)-pent-4-ene 
• 881015-88-9 (S)-2-((2S,3S,4R,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-ylmethyl)-pent-4-en-1-ol 
• 506410-39-5 (R)-4-benzyl-3-[3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)propionyl]oxazolidin-2-one 

Relevant academic research and scientific papers

Adaptable synthesis of C-glycosidic multivalent carbohydrates and succinamide-linked derivatization

A modular approach to the synthesis of trivalent C-glycosidic carbohydrates is described. The approach is illustrated employing carboxylate-terminated C-glycosidic d-mannose, d-glucose, and d-galactose derivatives with different length C1-linked spacer un

Synthesis of a C-glycoside analogue of β-D-galactosylthreonine

A C-linked analogue of β-D-galactosylthreonine has been prepared from 2,3,4,6-tetra-O-benzyl-D-galactopyranolactone (1) in 14 steps. Three stereogenic centers were created during the synthesis, with the anomeric center of the C-glycoside being generated f