152231-17-9

Upstream product

• 17342-08-4 (S)-5-Hydroxymethyl-4,5-dihydro-3H-pyrrol-2-ol 
• 109063-57-2 Acetic acid (S)-5-hydroxy-3,4-dihydro-2H-pyrrol-2-ylmethyl ester 
• 152231-15-7 ((2S,5R)-5-Methyl-pyrrolidin-2-yl)-methanol 
• 4931-66-2 (S)-5-Hydroxy-3,4-dihydro-2H-pyrrole-2-carboxylic acid methyl ester 
• 152189-89-4 ((S)-5-Methyl-3,4-dihydro-2H-pyrrol-2-yl)-methanol 
• 135649-90-0 (2S,5R)-1-(benzyloxycarbonyl)-2-(hydroxymethyl)-5-methylpyrrolidine 
• 41693-09-8 (2-oxononanylidene)triphenylphosphorane 
• 135625-68-2 (2S,5R)-2-Formyl-5-methyl-pyrrolidine-1-carboxylic acid benzyl ester 
• 152189-90-7 Acetic acid (S)-5-ethoxy-3,4-dihydro-2H-pyrrol-2-ylmethyl ester 
• 37497-25-9 dimethyl (2-oxononyl)-phosphonate 

Downstream Products

• 138723-03-2 (2S,5R)-1-(Carbobenzyloxy)-2-(3-oxodecyl)-5-methylpyrrolidine 

Relevant academic research and scientific papers

A new synthesis of ant venom alkaloid: (3S,5R,8S)-3-heptyl-5-methylpyrrolizidine

A highly enantioselective synthesis of (3S,5R,8S)-3-heptyl-5-methylpyrrolizidine is described by using (S)-pyroglutamic acid as starting material.

A chirospecific synthesis of an ant venom alkaloid (5Z,8E)-3-heptyl-5-methylpyrrolizidine

A straightforward and practical route for the chirospecific synthesis of both enantiomers of the ant venom alkaloid (5Z,8E)-3-heptyl-5-methylpyrrolizidine has been developed.