805247-68-1

Upstream product

• 850166-83-5 6-(4-methoxybenzyloxy)-hex-2-enoic acid ethyl ester 
• 2746-25-0 p-Methoxybenzyl bromide 
• 119649-45-5 4-(p-methoxybenzyloxy)butan-1-ol 
• 119649-27-3 4-((4-methoxybenzyl)oxy)butanal 

Downstream Products

• 805247-70-5 (2S,3S)-2-azido-3-hydroxy-6-(4-methoxy-benzyloxy)-hexanoic acid ethyl ester 
• 208649-02-9 (2S,3S)-3-hydroxypipecolic acid 
• 850166-89-1 4-[3-(4-methoxybenzyloxy)propyl]-2,2-dimethyl-5-(pent-3-en-1-ynyl)-[1,3]dioxolane 
• 850166-90-4 4-[3-(4-methoxybenzyloxy)propyl]-2,2-dimethyl-5-(penta-1,3-dienyl)[1,3]dioxolane 
• 850166-87-9 4-(2,2-dibromovinyl)-5-[3-(4-methoxybenzyloxy)propyl]-2,2-dimethyl-[1,3]dioxolane 
• 850166-88-0 4-ethynyl-5-[3-(4-methoxybenzyloxy)propyl]-2,2-dimethyl-[1,3]dioxolane 
• 850166-85-7 {5-[3-(4-methoxybenzyloxy)propyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}methanol 
• 850166-86-8 (4R,5S)-5-[3-(4-Methoxy-benzyloxy)-propyl]-2,2-dimethyl-[1,3]dioxolane-4-carbaldehyde 
• 850166-84-6 5-[3-(4-methoxybenzyloxy)propyl]-2,2-dimethyl-[1,3]dioxolane-4-carboxylic acid ethyl ester 
• 805247-69-2 (4R,5S)-5-[3-(4-Methoxy-benzyloxy)-propyl]-2,2-dioxo-2λ⁶-[1,3,2]dioxathiolane-4-carboxylic acid ethyl ester 

Relevant academic research and scientific papers

An asymmetric dihydroxylation route to (2S,3S)-3-hydroxypipecolic acid

A concise enantioselective synthesis of (2S,3S)-3-hydroxypipecolic acid 1 starting from 1,4-butanediol using Sharpless asymmetric dihydroxylation and the regioselective nucleophilic opening of a cyclic sulfate as the key steps is described. A concise enan

Efficient total synthesis of sapinofuranone B

(Chemical Equation Presented) An efficient enantioselective synthesis of sapinofuranone B (1) using Sharpless asymmetric dihydroxylation, Sonogashira coupling, and Wittig olefination as the key steps is described.