120211-82-7

Upstream product

• 187462-99-3 (2R,3S,4R)-3-Methoxycarbonylmethyl-4-vinyl-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 
• 188000-81-9 (2R,3S,4R)-4-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-3-(2-oxo-ethyl)-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 
• 120229-00-7 (2R,3S,4R)-3-Methoxycarbonylmethyl-4-[2-(4-methoxy-phenoxy)-ethyl]-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 
• 120251-75-4 (3R,3aS,5R,7aR)-1-Benzyl-5-benzyloxymethyl-3-[2-(4-methoxy-phenoxy)-ethyl]-hexahydro-pyrano[3,4-b]pyrrol-7-one 
• 120211-88-3 (2R,3S,4R)-3-Carboxymethyl-4-[2-(4-methoxy-phenoxy)-ethyl]-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 
• 120211-87-2 (2R,3S,4R)-3-((R)-2,3-Dihydroxy-propyl)-4-[2-(4-methoxy-phenoxy)-ethyl]-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 
• 120211-81-6 (3R,3aS,5R,7aR)-5-Hydroxymethyl-3-[2-(4-methoxy-phenoxy)-ethyl]-7-oxo-hexahydro-pyrano[3,4-b]pyrrole-1-carboxylic acid benzyl ester 
• 120211-76-9 (Z)-(R)-1-Benzyloxy-7-(4-methoxy-phenoxy)-hept-4-en-2-ol 
• 120211-75-8 (R)-1-Benzyloxy-7-(4-methoxy-phenoxy)-hept-4-yn-2-ol 
• 120211-80-5 (3R,3aS,5R,7aR)-5-Hydroxymethyl-3-[2-(4-methoxy-phenoxy)-ethyl]-hexahydro-pyrano[3,4-b]pyrrol-7-one 
• 187462-98-2 (2R,3S,4R)-3-(2-Oxo-ethyl)-4-vinyl-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 
• 188000-79-5 (2R,3S,4R)-4-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-3-[1,3]dithian-2-ylmethyl-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 

Downstream Products

• 120211-83-8 (2R,3S,4R)-3-Methoxycarbonylmethyl-4-(2-oxo-ethyl)-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 

Relevant academic research and scientific papers

An enantioconvergent route to(-)-kainic acid

A new stereocontrolled route to (-)-kainic acid, the representative of the kainoid amino acids and exhibiting insecticidal, anthelmintic and neuroexcitatory properties, has been devised in an enantioconvergent way using either (+)- or (-)-ketodicyclopentadiene as the starting material by employing a concurrent retro-Diels-Alder reaction and intramolecular ene reaction as the key step.

A new enantiocontrolled route to (-)-kainic acid

A new route to (-)-kainic acid, the parent member of the kainoids, has been developed using (+)-norcamphor as the starting material.

A Concise Enantioselective Route to (-)-Kainic acid from (S)-2-(Benzyloxymethyl)oxirane

A concise enantioselective route to (-)-kainic acid (1) from (S)-2-(benzyloxymethyl)oxirane (2) has been established by enentio- and diastereo-selective intramolecular 1,3-dipolar cyclization.