631918-12-2

Upstream product

• 100-39-0 benzyl bromide 
• 221044-94-6 (3aS,4S,5aR,9aR,9bS)-4-Benzyloxy-2,2,8,8-tetramethyl-hexahydro-[1,3]dioxolo[4',5':3,4]benzo[1,2-d][1,3]dioxin-5-one 
• 357604-61-6 2,3:4,6-di-O-isopropylidene-D-mannopyranose 
• 75-15-0 carbon disulfide 
• 221044-95-7 (3aR,4R,5R,5aS,9aR,9bS)-4-(benzyloxy)-2,2,8,8-tetramethylhexahydro-3aH-[1,3]dioxolo[4,5-h][1,3]benzodioxin-5-ol 
• 74-88-4 methyl iodide 
• 221044-98-0 1-phenyl-1,2-dideoxy-7-O-(phenoxythiocrbonyl)-4,5:6,8-di-O-isopropylidene-3-O-(tert-butyldimethylsilyl)-D-talo-D-glycero-oct-1-yne 
• 221044-97-9 1-phenyl-1,2-dideoxy-4,5:6,8-di-O-isopropylidene-3-O-(tert-butyldimethylsilyl)-D-talo-D-glycero-oct-1-yne 
• 221044-99-1 (3aS,4R,5aR,9aR,9bS)-5-benzylidene-2,2,8,8-tetra-methylhexahydro-3aH-[1,3]dioxolo[4,5-h][1,3]benzodioxin-4-yl tert-butyl(dimethyl)silyl ether 
• 631918-11-1 (3aR,4R,5aR,9aR,9bS)-5-benzylidene-4-(benzyloxy)-2,2,8,8-tetramethylhexahydro-3aH-[1,3]dioxolo[4,5-h][1,3]benzodioxine 
• 221044-89-9 1-phenyl-1,2-dideoxy-4,5:6,8-di-O-isopropylidene-D-talo-D-glycero-oct-1-yne 

Downstream Products

• 90694-06-7 (1R,2R,3S,4R,5R)-1,2,3,4-tetra-acetoxy-5-(acetoxymethyl)cyclohexane 
• 631918-13-3 2,3,4,6-tetra-O-acetyl-1-O-benzyl-5a-carba-β-D-mannopyranose 
• 90694-07-8 pseudo-β-D-mannopyranose 
• 221044-96-8 2,3:4,6-di-O-isopropylidene-1-O-benzyl-5a-carba-β-D-mannopyranose 

Relevant academic research and scientific papers

Stereodivergent synthesis of 5a-carba-hexopyranoses from carbohydrates via 6-exo-dig radical cyclization: Preparation of 5a-carba-β-D-manno-, α-D-allo-, β-L-talo- and α-L-gulopyranose pentaacetates from D-mannose

Four carbasugars, 5a-carba-β-D-manno-, α-D-allo-, β-L-talo- and α-L-gulopyranose pentaacetates, have been prepared in a stereodivergent manner from D-mannose. Alkynyl derivatives of 2,3:4,6-di-O-isopropylidene-D-mannopyranose, which are prepared by homolo

A novel entry to 5a-carba-hexopyranoses from carbohydrates based on a 6-exo-dig radical cyclization: Synthesis of 5a-carba-β-D-mannopyranose pentaacetate

Carbohydrate-derived 2,3:4,6-diacetonides which are homologated at C-1 by reaction with phenyl acetylide undergo a 6-exo-dig radical cyclization, from a radical located at C-5, to yield highly functionalized cyclohexanes that are correlated with carba-sugars.