403501-56-4

Upstream product

• 94840-08-1 2,3-O-isopropylidene-L-gulono-γ-lactone 
• 76-83-5 trityl chloride 
• 124-63-0 methanesulfonyl chloride 
• 294204-05-0 2,3-O-isopropylidene-6-O-triphenylmethyl-L-glucono-γ-lactone 

Relevant academic research and scientific papers

Combinatorial library approach to iminocyclitols with biological activity

A method of synthesizing stereochemically defined iminocyclitol comprises replacing an intraring oxygen in a cyclic sugar by an intraring imine to form an iminocyclitol, wherein said iminocyclitol has a defined stereochemical configuration different from

Bicyclic diazasugars. Part 3: β-D-Mannose and 6-deoxy-β-L-gulose analogues

A bicyclic analogue of β-D-mannopyranose with nitrogen atoms replacing the ring and glycosidic oxygen atoms has been prepared in a single step from 5-O-mesyl-D-mannofuranose by a process that likely involves double displacement and an epoxide intermediate. A similar but protected bicyclic analogue of 6-deoxy-β-L-gulopyranose has been prepared by an electrophilic cyclization reaction.