6586-63-6

Upstream product

• 6586-64-7 1,2:3,5-Di-O-isopropylidene-D-glycero-L-gulo-heptitol 
• 4258-03-1 5,6-O-isopropylidene-D-glusose diethyl dithioacetal 
• 140686-66-4 3-O-tert-butyldimethylsilyl-2,4:5,6-di-O-isopropylidene-D-glucose diethyl dithioacetal 
• 140686-65-3 (1R,2S,3R)-2-(tert-Butyl-dimethyl-silanyloxy)-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4,4-bis-ethylsulfanyl-butane-1,3-diol 
• 89-67-8 α-D-glucoheptonic γ-lactone 
• 6605-22-7 3,5:6,7-bis-O-(1-methylethylidene)-α-D-glucoheptonic γ-lactone 
• 140686-67-5 2,4:5,6-di-O-isopropylidene-D-glucose diethyl dithioacetal 

Downstream Products

• 141882-84-0 1,3-di-O-acetyl-2,4:5,6-di-O-isopropylidene-1-C-phenyl-D-glycero-D-gulo-hexitol 
• 141882-83-9 1-O-Acetyl-2,4:5,6-di-O-isopropylidene-1-C-phenyl-D-glycero-D-ido-hexitol 
• 141882-82-8 2,4:5,6-Di-O-isopropylidene-1-C-phenyl-D-glycero-D-ido-hexitol 
• 141882-82-8 2,4:5,6-Di-O-isopropylidene-1-C-phenyl-D-glycero-D-gulo-hexitol 
• 141882-82-8 (4S,5R,6S)-4-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-6-(hydroxy-phenyl-methyl)-2,2-dimethyl-[1,3]dioxan-5-ol 
• 141882-85-1 2,4:5,6-Di-O-isopropylidene-1-C-phenyl-D-gluco-hex-1-ulose 

Relevant academic research and scientific papers

Stereoselective Syntheses of 2,4:5,6-Di-O-isopropylidene-1-C-phenyl-D-glycero-D-ido-hexitol and 2,4:5,6-Di-O-isopropylidene-1-C-phenyl-D-glycero-D-gulo-hexitol from D-glycero-D-gulo-Heptono-γ-lactone. X-Ray Structure of 1-O-Acetyl-2,4:5,6-di-O-isopropylid

D-glycero-D-gulo-Heptonolactone has been converted by three consecutive reactions (acetonation, reduction and glycol cleavage reaction) into 2,4:5,6-di-O-isopropylidene-D-glucose which with phenylmagnesium bromide gave preponderantly 2,4:5,6-di-O-isopropy