102717-45-3

Upstream product

• 102717-39-5 (S)-1-(tert-Butyl-diphenyl-silanyloxy)-3-((R)-2,2-diethyl-[1,3]dioxolan-4-yl)-propan-2-ol 
• 102717-30-6 (3R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-3-hydroxy-dihydro-furan-2-one 
• 92512-38-4 (2R,4S)-5-(tert-Butyl-diphenyl-silanyloxy)-pentane-1,2,4-triol 
• 102717-41-9 (R)-2,2-Diethyl-4-(R)-1-oxiranylmethyl-[1,3]dioxolane 
• 102717-42-0 5-((R)-2,2-Diethyl-[1,3]dioxolan-4-yl)-4-hydroxy-2-phenylsulfanyl-pentanoic acid 
• 102717-43-1 (R)-5-((R)-2,2-Diethyl-[1,3]dioxolan-4-ylmethyl)-3-phenylsulfanyl-dihydro-furan-2-one 
• 102717-29-3 (5S)-5-({[tert-butyl(diphenyl)silyl]oxy}methyl)dihydrofuran-2(3H)-one 
• 102916-19-8 (S)-5-[(R)-3-(tert-Butyl-diphenyl-silanyloxy)-2-hydroxy-propyl]-dihydro-furan-2-one 

Downstream Products

• 102717-38-4 Acetic acid (1R,3S,5R)-3,5,6-triacetoxy-1-(tert-butyl-diphenyl-silanyloxymethyl)-hexyl ester 
• 102717-37-3 (2R,4S,6R)-7-(tert-Butyl-diphenyl-silanyloxy)-heptane-1,2,4,6-tetraol 

Relevant academic research and scientific papers

A Tactically Novel Alternative to Acyclic Stereoselection Based on the Concept of a Replicating Chiron - Access to 1,3-Polyols

(S)-Glutamic acid is used as a chiral template to construct seven carbon subunits containing alternating hydroxyl groups with stereochemical control.Enantiomeric and/or diastereomeric 3,5-dideoxy-heptitols are thus obtained.