156487-67-1

Upstream product

• 63699-97-8 1,2:5,6-dianhydro-3,4-O-methylethylidene-L-iditol 
• 156487-65-9 (4S,5S)-4,5-Bis-[(S)-2-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxolane 
• 156487-66-0 (S)-2-(tert-Butyl-diphenyl-silanyloxy)-2-{(4S,5S)-5-[(S)-1-(tert-butyl-diphenyl-silanyloxy)-2-hydroxy-ethyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-ethanol 
• 134896-17-6 1,6-di-O-benzyl-3,4-O-methylethylidene-L-iditol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 175166-58-2 (S)-1-[(4R,5R)-5-((S)-1-Hydroxy-allyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-prop-2-en-1-ol 
• 175275-70-4 3-[(4R,5R)-5-(3-hydroxy-1-(E)-propen-1-yl)-2,2-dimethyl[1,3]dioxolan-4-yl]-prop-2-(E)-en-1-ol 
• 73346-73-3 (4S,5S)-diethyl 2,2-dimethyl-1,3-dioxolane-4,5-dicarboxylate 

Relevant academic research and scientific papers

Facile asymmetric synthesis of the D-myo-inositol derivative from diethyl 2,3-O-isopropylidene-D-tartrate

A facile asymmetric synthesis of the D-myo-inositol derivative was achieved from diethyl 2,3-O-isopropylidene-D-tartrate in 7 steps. The two carboxylate groups of diethyl tartrate were converted simultaneously into dialdehyde to afford a key intermediate

A Stereoselective Route to Enantiomerically Pure myo-Inositol Derivatives Starting from D-Mannitol

A carbocyclization route to inositols starting from alditols has been developed involving as a key step a stereoselective intramolecular pinacol coupling of a 1,6-dialdehyde promoted by samarium diiodide.This route has been applied to the synthesis of ena