88171-39-5

Upstream product

• 34591-98-5 (E)-6-(benzyloxy)hex-3-en-2-one 
• 34591-98-5 6-Benzyloxy-3-hexen-2-on 
• 103871-46-1 3-Ethoxycarbonylmethyl-5-(2-hydroxy-ethyl)-4-methyl-thiazol-3-ium; bromide 

Downstream Products

• 88171-41-9 N-t-butoxycarbonyl-3α-(2-benzyloxyethyl)-4β-acetyl-α-proline-ethyl-ester 
• 88171-40-8 (2S,3R)-4-Acetyl-3-(2-benzyloxy-ethyl)-2,3-dihydro-1H-pyrrole-2-carboxylic acid ethyl ester 
• 487-79-6 (+/-)-(2S,3S,4R)-3-(carboxymethyl)-4-(prop-1-en-2-yl)pyrrolidine-2-carboxylic acid 
• 103871-61-0 (2S,3R,4R)-4-Acetyl-3-(2-benzyloxy-ethyl)-pyrrolidine-2-carboxylic acid ethyl ester 
• 103871-60-9 (2S,3R)-4-Acetyl-3-(2-benzyloxy-ethyl)-1-(2-methyl-3-methylsulfanyl-tetrahydro-furan-2-yl)-2,3-dihydro-1H-pyrrole-2-carboxylic acid ethyl ester 

Relevant academic research and scientific papers

The synthesis of amino acids by 1,3-dipolar cycloadditions of azomethine ylides

Thiazolium ylides react with a variety of dipolarophiles to afford adducts. After filtration chromatography, a tricyclic adduct is obtained. The tricyclic adducts react with potassium t-butoxide/t-butanol to provide dihydropyrroles. The adducts also react

THE TOTAL SYNTHESIS OF α-ALLOKAINIC ACID

The aminoacid α-allokainic acid was synthesized in eight steps from thiazolidine 2.