141882-83-9

Upstream product

• 6586-63-6 2,4:5,6-Di-O-isopropylidene-D-glucose 
• 108-24-7 acetic anhydride 

Downstream Products

• 141882-84-0 1,3-Di-O-acetyl-2,4:5,6-di-O-isopropylidene-1-C-phenyl-D-glycero-D-ido-hexitol 
• 144336-35-6 (E)-methyl 7-O-acetyl-4,6-O-isopropylidene-7-C-phenyl-D-ido-hept-2-enoate 
• 144336-35-6 (Z)-methyl 7-O-acetyl-4,6-O-isopropylidene-7-C-phenyl-D-ido-hept-2-enoate 
• 144336-37-8 2-deoxy-4,6-O-isopropylidene-3-O-methyl-7-C-phenyl-D-glycero-L-ido-heptono-δ-lactone 
• 144336-38-9 5-O-acetyl-2,4-O-isopropylidene-5-C-phenyl-D-ido-pentose 
• 144829-38-9 (Z)-methyl 4,6-O-isopropylidene-7-C-phenyl-D-ido-hept-2-enoate 
• 143892-96-0 2,4-O-isopropylidene-1-C-phenyl-D-glycero-D-ido-hexitol 
• 144829-40-3 2,4-O-isopropylidene-5-C-phenyl-D-ido-pentose 
• 144336-34-5 1-O-acetyl-2,4-O-isopropylidene-1-C-phenyl-D-glycero-D-iodo-hexitol 
• 141882-82-8 2,4:5,6-Di-O-isopropylidene-1-C-phenyl-D-glycero-D-ido-hexitol 

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