131403-22-0

Upstream product

• 131403-21-9 (2S,5R)-1-benzyloxycarbony-2-butyl-5-(hydroxymethyl)pyrrolidine 

Downstream Products

• 131403-23-1 (2S,5R)-1-benzyloxycarbonyl-2-butyl-5-(1-heptenyl)pyrrolidine 
• 95587-13-6 (+)-(S)-trans-2-heptyl-5-butyl-1-phenyl sulfonyl pyrrolidine 
• 95587-14-7 (+)-(S)-trans-2-heptyl-5-butylpyrrolidine 
• 131403-25-3 (2S,5S)-1-benzenesulfonyl-2-butyl-5-pentylpyrrolidine 
• 131403-24-2 (2S,5R)-1-benzyloxycarbonyl-2-butyl-5-(1-pentenyl)pyrrolidine 
• 142925-66-4 (2S,5S)-N-<(benzyloxy)carbonyl>-5-butyl-2-(4-hydroxybutyl)pyrrolidine 
• 142925-67-5 (2S,5S)-N-<(benzyloxy)carbonyl>-5-butyl-2-(4-oxobutyl)pyrrolidine 

Relevant academic research and scientific papers

AN ASYMMETRIC SYNTHESIS OF (+)-INDOLIZIDINE 195B

An asymmetric synthesis of (+)-indolizidine 195B (1) starting from the known pyrrolidino alcohol (2) available from L-norleucine has been achieved.

An Efficient Route to Chiral trans-2,5-Dialkylpyrrolidines via Stereoselective Intramolecular Amidomercuration

An intramolecular amidomercuration of α-butylated 4-pentenylcarbamate 5 predominantly provided trans-2,5-disubstituted pyrrolidine 6, which was elaborated to chiral trans-5-butyl-2-alkylpyrrolidines 10 and 13, constituents of ant venoms.