483341-82-8

Upstream product

• 63087-96-7 methyl 5-deoxy-5-iodo-2,3-O-isopropylidene-α-D-lyxofuranoside 
• 106-95-6 allyl bromide 
• 100-46-9 benzylamine 

Downstream Products

• 483341-83-9 (3S,4R,5R)-3,4-O-isopropylidene-5-(N-benzyl)-o-nitro-benzensulfon-amino-octa-1,7-diene-3,4-diol 
• 688334-55-6 C₃₈H₄₆N₄O₁₁S₂SiCCH₂OCH₂ 
• 688334-52-3 C₃₈H₄₆N₄O₁₁S₂Si 
• 688334-50-1 (1S,4S,6R)-4,6-bis[(N-benzyl)-o-nitrobenzenesulfon-amino]-1-O-(tert-butyldimethylsilyl)-cyclohex-2-enol 
• 688334-49-8 Acetic acid (1S,4S,6R)-4,6-bis-[benzyl-(2-nitro-benzenesulfonyl)-amino]-cyclohex-2-enyl ester 
• 483341-86-2 (1S,4S,6R)-4,6-bis[(N-benzyl)-o-nitrobenzenesulfon-amino]-cyclohex-2-enol 
• 483341-84-0 (1R,2S,6R)-6-(N-benzyl)-o-nitrobenzenesulfonamino-1,2-O-isopropylidene-cyclohex-3-en-1,2-diol 
• 483341-85-1 (1R,2S,6R)-6-(N-benzyl)-o-nitrobenzenesulfonamino-1,2-di-O-carbonyl-cyclohex-3-ene-1,2-diol 

Relevant academic research and scientific papers

A stereoselective route towards highly functionalized 4,6-diaminocyclohexene derivatives

A flexible synthetic route towards chirally pure 4,6-diaminocyclohexene derivatives based on palladium catalyzed allylic amination of carbohydrate derived cyclohexenes is presented.