671199-46-5

Upstream product

• 359714-90-2 (2R,3S,4R)-2,3,4-tris(benzyloxy)hex-5-enoic acid 
• 73111-58-7 2,3,4-tri-O-benzyl-5,6-dideoxy-D-xylo-hex-5-enose 
• 85716-43-4 methyl 6-deoxy-6-iodo-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 671199-53-4 (+)-(1S,2R,3R,4S,6S)-1,2,3-tribenzyloxy-4-tert-butyldimethylsilyloxy-6-mesyloxycyclohexane 
• 85716-45-6 1L-(2,4,5/3)-2,3,4-Tri-O-benzyl-2,3,4,5-tetrahydroxy-1-cyclohexanon 
• 800408-98-4 (1S,4S,5S,6S)-4,5,6-tris(benzyloxy)cyclohex-2-enol 
• 671199-55-6 (-)-(1S,2S,3R,4S,5R)-2,3,4-tribenzyloxy-5-mesyloxycyclohexanol 
• 131289-28-6 (2S,3R,4R,5S) 5-<(t-butyldimethylsilyl)oxy>-2,3,4-tris(benzyloxy) cyclohexane-1-one 
• 131289-29-7 (+)-(1R,2R,3S,4R,5S)-2,3,4-tribenzyloxy-5-(tert-butyldimethylsilyloxy)cyclohexanol 

Downstream Products

• 1053641-05-6 Phosphoric acid benzyl ester (R)-2-benzyloxy-3-hexadecyloxy-propyl ester (1R,2R,3S,4R)-2,3,4-tris-benzyloxy-cyclohexyl ester 
• 801297-68-7 1D-2,3-anhydro-4,5,6-tri-O-benzyl-myo-inositol 
• 197896-27-8 Diisopropyl-phosphoramidous acid benzyl ester (1R,2R,3S,4R)-2,3,4-tris-benzyloxy-cyclohexyl ester 
• 197896-26-7 1D-4,5,6-tri-O-benzyl-2,3-dideoxy-myo-inositol 
• 220564-16-9 (-)-(1R,2S,3S,4R)-2,3,4-tribenzyloxy-5-cyclohexene-1-ol 
• 98485-58-6 (-)-(2R,3S,4R)-2,3,4-trihydroxycyclohexanone 

Relevant academic research and scientific papers

Synthesis of polyhydroxylated decalins via two consecutive one-pot reactions: 1,4-Addition/aldol reaction followed by RCM/syn-dihydroxylation

Synthesis of novel polyhydroxylated derivatives of decalin is described. The presented methodology consists in a one-pot copper-catalyzed 1,4-addition of vinylmagnesium bromide to sugar-derived cyclohexenone, followed by an aldol reaction with a derivativ

Synthesis of (+)-(2R,3S,4R)-2,3,4-trihydroxycyclohexanone from D-glucose

We have described the synthesis of (+)-(2R,3S,4R)-2,3,4- trihydroxycyclohexanone by the reduction of a keto-conduritol derivative, the latter being prepared in five steps from (-)-(2S,3R,4S,5S)-2,3,4-tribenzyloxy-5- hydroxycyclohexanone, which is in turn

Synthesis of anti-tumour phosphatidylinositol analogues from glucose by the use of ring-closing olefin metathesis

A divergent strategy is described for synthesis of the novel phosphatidylinositols 1-3. The synthetic approach commences from benzyl-protected methyl 6-iodo-6-deoxy-α-D-glucopyranoside, which undergoes zinc-mediated reductive fragmentation followed by vin