944064-95-3

Upstream product

• 220688-25-5 O-(2-azido-3,4,6-tri-O-benzyl-2-deoxy-α/β-D-glucopyranosyl) trichloroacetimidate 
• 201800-34-2 3,4-di-O-benzyl-6-O-(tert-butyldiphenylsilyl)-D-galactal 
• 130323-37-4 (2R,3R,4R)-(3,4-bis(benzyloxy)-3,4-dihydro-2H-pyran-2-yl)methanol 
• 944064-93-1 O-(2-azido-2-deoxy-3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->6)-3,4-di-O-benzyl-D-galactal 
• 944064-94-2 O-(2-azido-2-deoxy-3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->6)-3,4-di-O-benzyl-2-deoxy-2-nitro-D-galactal 
• 71630-31-4 N-(tert-butyloxycarbonyl)-L-serine tert-butyl ester 

Downstream Products

• 944064-96-4 O-(2-acetamido-2-deoxy-3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->6)-3,4-di-O-benzyl-2-deoxy-2-nitro-D-galactopyranosyl)-N-(t-butyloxycarbonyl)-L-serine tert-butyl ester 
• 1053708-40-9 C₆₁H₇₇N₃O₁₄ 

Relevant academic research and scientific papers

Glycal glycosylation and 2-nitroglycal concatenation, a powerful combination for mucin core structure synthesis

(Chemical Equation Presented) A 3,4-O-unprotected galactal derivative having bulky 6-O-TIPS protection (compound 2) could be regioselectively 3-O-glycosylated with O-(galactopyranosyl) trichloroacetimidates; depending on the protecting group pattern stere