219562-68-2

Upstream product

• 219562-50-2 (R)-2-Benzyloxy-2-[(4S,5S)-5-((R)-1-benzyloxy-2-hydroxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethanol 

Downstream Products

• 219562-34-2 (2S,3S,4S,5S)-1-Benzyl-3,4-bis-methoxymethoxy-2,5-bis-methoxymethoxymethyl-pyrrolidine 
• 219562-80-8 (2S,3S,4S,5S)-1-Benzyl-2,5-bis-hydroxymethyl-pyrrolidine-3,4-diol 
• 219562-20-6 (-)-(2R,5R)-dibenzyloxy-(3R,4S)-1,3,4,6-tetra(methoxymethyl) hexane 

Relevant academic research and scientific papers

Enantioselective approach to polyhydroxylated compounds using chiral sulfoxides: Synthesis of enantiomerically pure myo-inositol and pyrrolidine derivatives

A short enantioselective Synthesis of the biologically important myo- inositol derivative I and the pyrrolidine derivative II is described. The molecule 3, a diketo disulfoxide readily made from tartaric acid, is the key intermediate. The sulfinyl group controlled completely the very high stereoselection observed.