102208-56-0

Upstream product

• 93125-78-1 (R)-1,3,4-Tris-benzyloxy-hex-5-en-2-ol 
• 198775-13-2 ((3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-methanol 
• 102208-53-7 (3R,4R,5R)-5-hydroxy-3,4,6-tribenzyloxy-1-hexene 
• 102093-89-0 3,4,5,6-tetra-O-benzyl-1,2-dideoxy-D-gluc-1-enitol 
• 109066-13-9 3,4,6-tri-O-benzyl-5-O-<(2,6-dichlorophenyl)methyl>-1,2-dideoxy-D-gluc-1-enitol 
• 160549-10-0 2,3,5-tri-O-benzyl-D-arabinofuranose 
• 109065-81-8 C₂₇H₂₉BrHgO₄ 
• 109065-81-8 C₂₇H₂₉BrHgO₄ 
• 102208-54-8 2,5-anhydro-3,4,6-tri-O-benzyl-D-glucitol 
• 102208-55-9 2,5-anhydro-3,4,6-tri-O-benzyl-D-mannitol 
• 102093-89-0 C₃₄H₃₆O₄ 

Downstream Products

• 102208-59-3 2,5-anhydro-3,4-di-O-benzyl-1-bromo-1-deoxy-D-mannitol diphenyl 6-phosphate 
• 115149-88-7 2,5-anhydro-3,4-di-O-benzyl-1-deoxy-1-diphenoxyphosphinoyl-D-mannitol 
• 102208-58-2 (2R,3R,4R,5R)-3,4-di-O-benzyl-2-bromomethyl-5-hydroxymethyl tetrahydrofuran 
• 115166-41-1 2,5-anhydro-3,4-O-benzyl-1-deoxy-1-diphenoxyphosphinoyl-D-glucitol diphenyl 6-phosphate 
• 115149-89-8 2,5-anhydro-3,4-di-O-benzyl-1-deoxy-1-dimethoxyphosphinoyl-D-glucitol dimethyl 6-phosphate 
• 102208-57-1 Acetic acid (2R,3R,4S,5S)-3,4-bis-benzyloxy-5-bromomethyl-tetrahydro-furan-2-ylmethyl ester 
• 102093-92-5 Acetic acid (2R,3R,4S)-3,4-bis-benzyloxy-5-bromomethyl-tetrahydro-furan-2-ylmethyl ester 
• 116127-74-3 2,5-anhydro-3,4,6-tri-O-benzyl-1-deoxy-1-diphenoxyphosphinoyl-D-mannitol 
• 102093-93-6 ((2R,3R,4S)-3,4-Bis-benzyloxy-5-bromomethyl-tetrahydro-furan-2-yl)-methanol 
• 102093-94-7 2,5-anhydro-3,4-di-O-benzyl-1-bromo-1-deoxy-D-glucitol diphenyl 6-phosphate 
• 115149-88-7 2,5-anhydro-3,4-di-O-benzyl-1-deoxy-1-diphenoxyphosphinoyl-D-glucitol 
• 102093-93-6 2,5-anhydro-3,4-di-O-benzyl-1-bromo-1-deoxy-D-glucitol 
• 115149-90-1 2,5-anhydro-3,4,6-tri-O-benzyl-1-deoxy-1-diphenoxyphosphinoyl-D-glucitol 
• 102093-95-8 C₄₄H₄₂O₁₁P₂ 

Relevant academic research and scientific papers

Stereoselectivity of Electrophile-Promoted Cyclizations of γ-Hydroxyalkenes. An Investigation of Carbohydrate-Derived and Model Substrates

We have investigated cyclization reactions of γ-hydroxyalkenes bearing an alkoxy or alkyl substituent on the allylic carbon.A variety of electrophiles N-bromosuccinimide, N-iodosuccinimide, iodine, mercury(II) acetate, mercury(II) trifluoroacetate, mercu

STEREOSELECTIVITY IN THE ELECTROPHILE-MEDIATED CYCLIZATION OF 2,3,5-TRI-O-BENZYL-1,2-DIDEOXY-D-arabino-HEX-1-ENITOL. A STEREOCONTROLLED SYNTHESIS OF 1-AMINO-2,5-ANHYDRO-3,4,6-TRI-O-BENZYL-1-DEOXY-D-GLUCITOL

Cyclization of 2,3,5-tri-O-benzyl-1,2-dideoxy-D-arabino-hex-1-enitol (2) with mercuric acetate, mercuric trifluoroacetate, iodine, and N-bromosuccinimide gave preponderantly the allo isomer of the C-arabinofuranosyl structure. 1-Amino-2,5-anhydro-3,4,6-tr

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