143564-22-1

Upstream product

• 143465-64-9 (1S,2S,3R,4R,5R)-3,4-di-O-benzyl-2-benzylamino-5-C-hydroxymethyl-1,3,4-cyclohexanetriol 
• 106265-22-9 (3aS,4R,5R,7aS)-3-Benzyl-4,5-bis-benzyloxy-6-hydroxymethyl-hexahydro-benzooxazol-2-one 
• 106265-19-4 (1S,2S,3R,4R)-3,4-di-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-methoxymethylene-1,3,4-cyclohexanetriol 
• 106265-22-9 (1S,2S,3R,4R,5R)-3,4-di-O-benzyl-2-benzylamino-1,2-N,O-carbonyl-5-C-hydroxymethyl-1,3,4-cyclohexanetriol 
• 106265-18-3 2L-(2,4,5/3) 2,3-di-O-benzyloxy-4-N-benzyl-4-N-benzyloxycarbonyl-amino-5-hydroxy-cyclohexanone 
• 106265-18-3 benzyl benzyl((2R,3S)-2,3-bis(benzyloxy)-6-hydroxy-4-oxocyclohexyl)carbamate 

Downstream Products

• 143465-47-8 1D-(1,2,4/3,5)-3-O-<(R)-3-hydroxytetradecanoyl>-2-<(R)-3-hydroxytetradecanoylamido>-1-O-phosphono-5-C-hydroxymethyl-1,3,4-cyclohexanetriol 
• 143465-60-5 (R)-3-Benzyloxymethoxy-tetradecanoic acid (2R,4aR,6S,7R,8R,8aR)-7-((R)-3-benzyloxymethoxy-tetradecanoylamino)-6-(diphenoxy-phosphoryloxy)-2-phenyl-hexahydro-benzo[1,3]dioxin-8-yl ester 
• 143465-59-2 Phosphoric acid (2R,4aR,6S,7R,8R,8aR)-7-((R)-3-benzyloxymethoxy-tetradecanoylamino)-8-hydroxy-2-phenyl-hexahydro-benzo[1,3]dioxin-6-yl ester diphenyl ester 
• 143465-56-9 (R)-3-Hydroxy-tetradecanoic acid (1R,2R,3S,5R,6R)-3-(diphenoxy-phosphoryloxy)-6-hydroxy-5-hydroxymethyl-2-((R)-3-hydroxy-tetradecanoylamino)-cyclohexyl ester 
• 143465-58-1 (R)-3-Benzyloxymethoxy-tetradecanoic acid ((2R,4aR,6S,7S,8R,8aR)-6,8-dihydroxy-2-phenyl-hexahydro-benzo[1,3]dioxin-7-yl)-amide 
• 143465-65-0 (R)-3-Benzyloxymethoxy-tetradecanoic acid ((1S,2R,3R,4R,6S)-2,3,6-trihydroxy-4-hydroxymethyl-cyclohexyl)-amide 

Relevant academic research and scientific papers

Optimized and Scalable Synthesis of Carba-α-d-Glucosamine

An efficient, high-yielding synthesis of carba-α-d-glucosamine is reported. Key features of this optimized route include an innovative protecting group strategy and an unusual, stereoconvergent Ferrier carbocyclization of a hindered substrate. The sequenc

Synthesis of the carbon pseudosugar analog of lipid X

A carbocyclic analog (2) with a deactivated pseudo-anomeric phosphate of the lipopolysaccharide biosynthetic intermediate Lipid X (1) was prepared in order to better understand the biological behavior of the parent compound. Two related synthetic routes t