207564-34-9

Upstream product

• 207564-32-7 1,5-anhydro-di-O-benzyl-2,6,7-trideoxy-D-arabino-hept-1,6-dienitol 
• 129840-37-5 1,5-anhydro-3,4-di-O-benzyl-6-O-(tert-butyldimethylsilyl)-2-deoxy-D-arabino-hex-1-enitol 
• 136656-49-0 3,4-di-O-acetyl-1,5-anhydro-6-O-t-butyldimethylsilyl-2-deoxy-D-arabino-hex-1-enitol 
• 82295-98-5 3,4-di-O-acetyl-1,5-anhydro-2-deoxy-D-arabino-hex-1-enitol 
• 2873-29-2 D-glucal triacetate 
• 13265-84-4 D-glucal 
• 207564-33-8 (2S,3S,4R)-3,4-Bis-benzyloxy-3,4-dihydro-2H-pyran-2-carbaldehyde 
• 58871-10-6 3,4-di-O-benzyl-D-glucal 

Downstream Products

• 207564-31-6 1,5-anhydro-3,4-di-O-benzyl-2-deoxy-5a-carba-D-arabino-hex-1-enitol 
• 135820-00-7 5a-carba-α-D-mannopyranose 
• 94943-08-5 (1S)-(+)-(1,3/2,4,5)-2,3,4,5-tetrahydroxycyclohexanemethanol 
• 158250-56-7 (3R,4R,5R)-3,4-dibenzyloxy-5-(benzyloxymethyl)cyclohexene 
• 207564-35-0 3,4-di-O-benzyl-5a-carba-α-D-glucopyranose 
• 207564-36-1 (1S,2R,3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-cyclohexane-1,2-diol 
• 1236311-60-6 C₂₉H₄₄O₅Si 
• 1192260-17-5 1-O-acetyl-3,4-di-O-benzyl-6-O-thexyldimethylsilyl-5a-carba-α-D-glucopyranose 

Relevant academic research and scientific papers

Synthesis and preliminary biological evaluation of carba analogues from Neisseria meningitidis A capsular polysaccharide

The Gram-negative encapsulated bacterium Neisseria meningitidis type A (MenA) is a major cause of meningitis in developing countries, especially in the sub-Saharan region of Africa. The development and manufacture of an efficient glycoconjugate vaccine ag

Carbocyclic Substrate Analogues Reveal Kanosamine Biosynthesis Begins with the α-Anomer of Glucose 6-Phosphate

NtdC is an NAD-dependent dehydrogenase that catalyzes the conversion of glucose 6-phosphate (G6P) to 3-oxo-glucose 6-phosphate (3oG6P), the first step in kanosamine biosynthesis in Bacillus subtilis and other closely-related bacteria. The NtdC-catalyzed r

Carbohydrates to carbocycles: An expedient synthesis of pseudo-sugars

A short and versatile synthesis of pseudo-sugars from sugars utilizing the Claisen rearrangement as the key step is described.