1054764-29-2

Upstream product

• 6921-34-2 benzylmagnesium chloride 
• 153059-37-1 1,2:5,6-dianhydro-3,4-O-isopropylidene-L-mannitol 
• 153192-27-9 2,5-diazido-1,6-dibenzyl-3,4-O-isopropylidene-1,2,5,6-tetradeoxy-D-iditol 
• 153192-26-8 1,6-dibenzyl-3,4-O-isopropylidene-1,6-dideoxy-L-mannitol 
• 185450-11-7 2,5-diazido-1,6-dibenzyl-3,4-bis-O-[(2-methoxyethoxy)methyl]-1,2,5,6-tetradeoxy-D-iditol 
• 185450-08-2 2,5-diazido-1,6-dibenzyl-1,2,5,6-tetradeoxy-D-iditol 

Downstream Products

• 185450-23-1 (3R,4S,5S,6R)-2,7-Dibenzyl-4,5-bis-(2-methoxy-ethoxymethoxy)-3,6-diphenethyl-[1,2,7]thiadiazepane 1,1-dioxide 
• 185450-17-3 (4R,5S,6S,7R)-1,3-Dibenzyl-5,6-bis-(2-methoxy-ethoxymethoxy)-4,7-diphenethyl-[1,3]diazepan-2-one 
• 185450-21-9 (3R,4S,5S,6R)-4,5-Bis-(2-methoxy-ethoxymethoxy)-3,6-diphenethyl-[1,2,7]thiadiazepane 1,1-dioxide 

Relevant academic research and scientific papers

Cyclic HIV-1 protease inhibitors derived from mannitol: Synthesis, inhibitory potencies, and computational predictions of binding affinities

Ten C2-symmetric cyclic urea and sulfamide derivatives have been synthesized from L-mannonic γ-lactone and D-mannitol. The results of experimental measurement of their inhibitory potencies against HIV-1 protease were compared to calculated free