749875-28-3

Upstream product

• 146986-42-7 ((2S,3S)-3-(2-(4-methoxybenzyloxy)ethyl) oxiran-2-yl)methanol 
• 172427-68-8 ethyl <2E>-5-(4-methoxybenzyloxy)-2-pentenoate 
• 135362-69-5 3-(4-methoxybenzyl)oxypropan-1-ol 
• 824-94-2 p-methoxybenzyl chloride 
• 158817-21-1 (E)-5-(4-methoxybenzyloxy)pent-2-en-1-ol 

Downstream Products

• 749875-18-1 (4S,5R)-4-[2-(4-Methoxy-benzyloxy)-ethyl]-2-phenyl-[1,3]dioxan-5-ol 
• 749875-22-7 2-((4S,5S)-5-Azido-2-phenyl-[1,3]dioxan-4-yl)-ethanol 
• 749875-20-5 (4S,5S)-5-Azido-4-[2-(4-methoxy-benzyloxy)-ethyl]-2-phenyl-[1,3]dioxane 
• 749875-25-0 (2R,3S)-4-((4S,5S)-5-Azido-2-phenyl-[1,3]dioxan-4-yl)-2,3-dihydroxy-butyric acid ethyl ester 
• 749875-26-1 (4R,5S)-5-((4S,5S)-5-Azido-2-phenyl-[1,3]dioxan-4-ylmethyl)-2-oxo-2λ⁴-[1,3,2]dioxathiolane-4-carboxylic acid ethyl ester 
• 847864-51-1 Methanesulfonic acid (4S,5R)-4-[2-(4-methoxy-benzyloxy)-ethyl]-2-phenyl-[1,3]dioxan-5-yl ester 

Relevant academic research and scientific papers

Enantioselective synthesis of (-)-galantinic acid

An efficient enantioselective synthesis of (-)-galantinic acid 1, a non-proteogenic amino acid is described using Sharpless asymmetric epoxidation, dihydroxylation and the regioselective nucleophilic opening of a cyclic sulfite as the key steps.