911028-36-9

Upstream product

• 114117-12-3 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->4)-1,5-anhydro-2-deoxy-3,6-di-O-benzyl-D-arabino-hex-1-enitol 
• 911028-31-4 (3R,4R,5R)-3,6-bis(benzyloxy)-4-(2',3',4',6'-tetra-O-benzyl-β-D-galactopyranosyl)hexane-1,5-diol 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 937176-40-4 C₅₅H₆₁N₃O₁₁S 

Relevant academic research and scientific papers

Glycals in organic synthesis: A systematic strategy for the preparation of uncommon piperidine 1,2-dideoxy-L-azasugars and 2-deoxy-1,5-anhydro-L-hexitols

A systematic synthetic strategy has been developed for producing uncommon piperidine 1,2-dideoxy-L-azasugars. This method involves the formation of open intermediates such as 2, 7, and 10 easily by ring-opening of D-glycals with aqueous mercury(II) acetat

A highly efficient and stereocontrolled synthesis of 2-deoxy-1,5- thioanhydro-L-hexitols from D-glycals in a tandem nucleophilic displacement reaction

2-Deoxy-1,5-thioanhydro-L-hexitols have been synthesized in a concise sequence that includes: i) ring opening of glycals with aqueous mercury(II) acetate/sodium borohydride; ii) mesylation of the free hydroxy groups of the multifunctionalized open interme