205505-38-0

Upstream product

• 2985-39-9 2-benzylmalonic acid monoethyl ester 
• 20593-63-9 2-Benzylacrylic acid ethyl ester 

Downstream Products

• 205505-43-7 (S)-2-Benzyl-2-hydroxy-3-(toluene-4-sulfonyloxy)-propionic acid ethyl ester 
• 205505-41-5 ((S)-4-Benzyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-[2-(2-methoxy-ethoxymethoxy)-phenyl]-methanone 
• 205505-42-6 (S)-2-Hydroxy-2-hydroxymethyl-1-(2-hydroxy-phenyl)-3-phenyl-propan-1-one 
• 205505-44-8 (R)-2-Bromomethyl-2-hydroxy-3-phenyl-propionic acid ethyl ester 
• 205505-40-4 (S)-4-Benzyl-2,2-dimethyl-[1,3]dioxolane-4-carbaldehyde 
• 223480-34-0 ethyl (R)-2-hydroxy-2-methyl-3-phenylpropanoate 
• 127184-10-5 (S)-3-Benzyl-3-hydroxy-chroman-4-one 
• 63742-14-3 (R)-(+)-2-hydroxy-2-methyl-3-phenylpropionic acid 
• 205505-39-1 (S)-4-Benzyl-2,2-dimethyl-[1,3]dioxolane-4-carboxylic acid ethyl ester 

Relevant academic research and scientific papers

Asymmetric organocatalytic synthesis of tertiary azomethyl alcohols: key intermediates towards azoxy compounds and α-hydroxy-β-amino esters

A series of peracylated glycosamine-derived thioureas have been synthesized and their behavior as bifunctional organocatalysts has been tested in the enantioselective nucleophilic addition of formaldehyde tert-butyl hydrazone to aliphatic α-keto esters fo

Asymmetric synthesis of (R)-(+)-etomoxir via enzymatic resolution

An asymmetric synthesis of (R)-(+)-etomoxir 3, employing enzymatic resolution of ethyl 2-alkyl-2,3-dihydroxypropionate using Amano AK via transacylation is reported. Copyright (C) 2000 Elsevier Science Ltd.

Enantioselective synthesis of eucomols using sharpless catalytic asymmetric dihydroxylation

A novel synthetic method was developed for eucomols, (S)-3-hydroxyhomoisoflavanones. Addition of aryllithium to aldehyde ((S)-9) obtained by asymmetric dihydroxylation of 4, followed by the formation of cyclic ether, gave eucomols, (S)-3-hydroxyhomoisofla