363619-57-2

Upstream product

• 545-06-2 trichloroacetonitrile 
• 61277-56-3 1,6-di-O-acetyl-2,3,4-tri-O-benzyl-α/β-D-galactopyranose 
• 363619-55-0 C₃₁H₂₈O₁₁ 
• 363619-56-1 C₂₉H₂₅BrO₉ 

Downstream Products

• 363619-62-9 C₄₈H₅₁O₁₈P 
• 363619-60-7 C₅₉H₅₅O₂₀P 
• 663622-37-5 C₄₁H₅₀O₁₀ 
• 634603-06-8 C₃₆H₃₂O₁₁ 
• 634603-15-9 C₅₈H₅₂O₁₉ 
• 663622-43-3 C₆₈H₇₂O₁₈ 
• 847225-70-1 isopropyl 6-O-acetyl-2,3,4-tri-O-benzoyl-β-D-galactopyranosyl-(1->6)-3-O-allyl-2,4-di-O-benzoyl-1-thio-β-D-galactopyranoside 
• 865294-16-2 4-methoxyphenyl 2,3,4-tri-O-benzoyl-β-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-β-D-galactopyranoside 
• 634603-11-5 4-methoxyphenyl 2,3,4-tri-O-benzoyl-β-D-galactopyranoside 
• 663622-38-6 C₃₉H₄₈O₉ 
• 663622-40-0 C₅₉H₆₆O₁₆ 
• 663622-39-7 C₆₃H₇₀O₁₈ 
• 663622-44-4 C₆₆H₇₀O₁₇ 
• 493012-77-4 C₅₇H₅₁O₂₀P 

Relevant academic research and scientific papers

An effective synthesis of an arabinogalactan with a β-(1->6)-linked galactopyranose backbone and α-(1->2) arabinofuranose side chains

An octasaccharide, β-D-Galp-(1->6)-[α-L-Araf-(1->2)]-β-D-Galp-(1->6)-β-D-Galp-(1->6)-[α-L-Araf-(1->5)-α-L-Araf-(1->2)]-β-D-Galp-(1->6)-β-D-Galp-1-> OMP was synthesized. 4-methoxyphenyl 2,3,4-tri-O-benzoyl-β-D-galactropyranoside (5), 2,6-di-O-acetyl-3,4-di

An Efficient Method for the Synthesis of 2,6-Branched Galacto- Oligosaccharides and Its Applications to the Synthesis of Three Tetrasaccharides and a Hexasaccharide Related to the Arabinogalactans (AGs)

An efficient method for the synthesis of 2,6-branched galacto- oligosaccharides has been developed by using 6-O-Ac-2,3,4-tri-O-Bz-α-D- galactopyranosyl trichloroacetimidate, 2,6-di-O-Ac-3,4-di-O-Bz-α-D- galactopyranosyl trichloroacetimidate and 2-O-Ac-3,4,6-tri-O-Bz-α-D- galactopyranosyl trichloroacetimidate as synthons. Three tetrasaccharides and a hexasaccharides related to AGs from plants were readily prepared using this method.

Synthesis of β-D-Galp-(1 →4)-α-D-Manp methanephosphonate, a substrate analogue for the elongating α-D-mannosyl phosphate transferase in the Leishmania

An isosteric C-glycoside phosphono analogue of dec-9-enyl β-D-galactopyranosyl-(1 →4)-α-D-mannopyranosyl phosphate was synthesised and showed high biological activity in the Leishmania MPT assay. A one-step Horner-Emmons/Michael reaction was developed for the stereoselective preparation of α-D-mannosyl methanephosphonate derivatives.