914982-48-2

Upstream product

• 257881-05-3 Methanesulfonic acid (1R,2S,3S,4R)-5-benzyloxy-1-benzyloxymethyl-2,3-dihydroxy-4-methanesulfonyloxy-pentyl ester 
• 226931-87-9 1,6-di-O-benzyl-2,5-di-O-methanesulfonyl-3,4-O-methylethylidene-D-mannitol 
• 142285-65-2 3,5-diazido-1,6-di-O-benzyl-2,5-dideoxy-3,4-O-methylethylidene-L-iditol 
• 142285-66-3 3,5-diamino-1,6-di-O-benzyl-2,5-dideoxy-3,4-O-methylethylidene-L-iditol 
• 151061-71-1 2,5-Di-O-mesyl-1,3:4,6-di-O-benzylidene-D-mannitol 
• 100-52-7 benzaldehyde 
• 69-65-8 mannitol 
• 61490-28-6 1,3:4,6-di-O-benzylidene-D-mannitol 
• 914982-45-9 (S)-2-benzyloxy-1-((4R,5R)-5-((S)-2-benzyloxy-1-(tosylamino)ethyl)-2,2-dimethyl-1,3-dioxolan-4-yl)-N-tosylethanamine 
• 914982-46-0 (2S,3R,4R,5S)-1,6-bis(benzyloxy)-2,5-bis(tosylamino)hexane-3,4-diol 
• 914982-47-1 (2R,3S,4S,5R)-1,6-bis(benzyloxy)-3,4-bis((methylsulfonyl)oxy)-N₂,N₅-ditosylhexane-2,5-diamine 

Relevant academic research and scientific papers

Synthesis of enantiopure bis-aziridines, bis-epoxides, and aziridino-epoxides from d-mannitol

A practical synthesis of enantiopure bis-aziridines 11 and 15, bis-epoxides 12 and 17, and aziridino-epoxides 27 and 30 is reported using inexpensive d-mannitol as the starting material. The key transformation involves the reductive cleavage of bis-benzyl