357604-61-6

Upstream product

• 3458-28-4 D-Mannose 
• 77-76-9 2,2-dimethoxy-propane 
• 530-26-7 D-Mannose 
• 116-11-0 2-Methoxypropene 

Downstream Products

• 221044-89-9 1-phenyl-1,2-dideoxy-4,5:6,8-di-O-isopropylidene-D-talo-D-glycero-oct-1-yne 
• 3458-28-4 D-Mannose 
• 640285-46-7 (3aS,6R,7R,7aS)-6-Hydroxymethyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4,7-diol 
• 631917-85-6 (4R,5R)-4-[(4R,5R)-5-((S)-1-Hydroxy-3-phenyl-prop-2-ynyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2,2-dimethyl-[1,3]dioxan-5-ol 
• 90694-06-7 (1R,2R,3S,4R,5R)-1,2,3,4-tetra-acetoxy-5-(acetoxymethyl)cyclohexane 
• 221044-96-8 2,3:4,6-di-O-isopropylidene-1-O-benzyl-5a-carba-β-D-mannopyranose 
• 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 
• 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 
• 631918-12-2 Dithiocarbonic acid O-((3aR,4R,5R,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-yl) ester S-methyl ester 
• 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 
• 221044-90-2 Carbonic acid ethyl ester (R)-1-[(4R,5S)-5-((4R,5R)-5-hydroxy-2,2-dimethyl-[1,3]dioxan-4-yl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-3-phenyl-prop-2-ynyl ester 
• 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 
• 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 

Relevant academic research and scientific papers

Straightforward synthesis of protected 2-hydroxyglycals by chlorination-dehydrochlorination of carbohydrate hemiacetals

A straightforward and scalable method for the synthesis of protected 2-hydroxyglycals is described. The approach is based on the chlorination of carbohydrate-derived hemiacetals, followed by an elimination reaction to establish the glycal moiety. 1,2-dehy

Enantiomerically pure 3-hydroxypropyl diisopropylidene mannose derivatives

Enantiomerically pure 3-hydroxypropyl diisopropylidene mannose derivatives were prepared and fully characterized. The procedure is generally applicable to monosaccharides and thus facilitates access to differently substituted glycosidic precursors.

An efficient catalysed ceric ammonium nitrate acetonation method for carbohydrates

A novel and efficient acetonation procedure promoted by ceric ammonium nitrate with dimethoxypropane in anhydrous N,N-dimethylformamide at room temperature is reported. The method has been advantageously developed for mono- and oligosaccharides.