102208-58-2

Upstream product

• 102208-56-0 2,5-anhydro-3,4,6-tri-O-benzyl-1-bromo-1-deoxy-D-altritol 
• 36199-02-7 3,4-di-O-benzyl-D-mannitol 
• 109065-81-8 C₂₇H₂₉BrHgO₄ 
• 102093-88-9 2,5-anhydro-3,4,6-tri-O-benzyl-1-bromo-1-deoxy-D-glucitol 
• 102208-54-8 2,5-anhydro-3,4,6-tri-O-benzyl-D-glucitol 
• 102093-89-0 C₃₄H₃₆O₄ 
• 93125-78-1 (R)-1,3,4-Tris-benzyloxy-hex-5-en-2-ol 
• 160549-10-0 2,3,5-tri-O-benzyl-D-arabinofuranose 
• 102093-92-5 Acetic acid (2R,3R,4S)-3,4-bis-benzyloxy-5-bromomethyl-tetrahydro-furan-2-ylmethyl ester 

Downstream Products

• 102208-59-3 2,5-anhydro-3,4-di-O-benzyl-1-bromo-1-deoxy-D-mannitol diphenyl 6-phosphate 
• 115224-25-4 ((2R,3S,4S,5R)-3,4-Dihydroxy-5-phosphonooxymethyl-tetrahydro-furan-2-ylmethyl)-phosphonic acid 
• 102093-94-7 Phosphoric acid (2R,3R,4S)-3,4-bis-benzyloxy-5-bromomethyl-tetrahydro-furan-2-ylmethyl ester diphenyl ester 

Relevant academic research and scientific papers

A practical approach to the synthesis of dianhydro sugars

Chiral tetrols derived from various carbohydrate precursors have been converted into the corresponding dianhydro sugar derivatives in a one pot procedure. The course of reaction very much depends upon the protecting groups used. In case of D-mannitol and

SYNTHESIS OF C-ARABINOFURANOSYL COMPOUNDS. PHOSPHONATE AND CARBOXYLATE ISOESTERS OF D-ARABINOSE 1,5-BISPHOSPHATE

Electrophile-mediated cyclization of 3,4,6-tri-O-benzyl-1,2-dideoxy-D-arabino-hex-1-enitol with N-bromosuccinimide yielded primarily 2,5-anhydro-3,4,6-tri-O-benzyl-1-bromo-1-deoxy-D-glucitol (10).This apparently kinetically controlled reaction was of key