306739-82-2

Upstream product

• 306739-80-0 benzyl (2S,3S)-2-but-3-enyl-5-oxo-3-[(R)-1-(2,4,6-triisopropylphenyl)ethoxy]pyrrolidine-1-carboxylate 
• 306739-76-4 (4S,5S)-5-but-3-enyl-3,3-dichloro-4-[(R)-1-(2,4,6-triisopropylphenyl)ethoxy]pyrrolidin-2-one 
• 306739-88-8 (4S,5S)-5-but-3-enyl-4-[(R)-1-(2,4,6-triisopropylphenyl)ethoxy]pyrrolidin-2-one 
• 501-53-1 benzyl chloroformate 
• 306740-01-2 (2S,3S)-2-But-3-enyl-5-hydroxy-3-[(R)-1-(2,4,6-triisopropyl-phenyl)-ethoxy]-pyrrolidine-1-carboxylic acid benzyl ester 

Downstream Products

• 306739-93-5 benzyl (2S,3S)-2-(3,4-dihydroxybutyl)-3-[(R)-1-(2,4,6-triisopropylphenyl)ethoxy]pyrrolidine-1-carboxylate 
• 306739-84-4 (1S,8aS)-1-[(R)-1-(2,4,6-triisopropylphenyl)ethoxy]octahydroindolizin-6-ol 
• 306739-97-9 (1S,8aS)-1-[(R)-1-(2,4,6-triisopropylphenyl)ethoxy]octahydroindolizin-6-one 
• 306739-95-7 benzyl (2S,3S)-2-(3-hydroxy-4-(toluene-4-sulfonyloxy)butyl)-3-[(R)-1-(2,4,6-triisopropylphenyl)ethoxy]pyrrolidine-1-carboxylate 

Relevant academic research and scientific papers

Highly Enantioselective Approach to Indolizidines: Preparation of (+)-(1S,8aS)-1-Hydroxyindolizidine and (-)-Slaframine

A highly stereoselective approach to (-)-slaframine and its probable biosynthetic precursor (+)-(1S,8aS)-1-hydroxyindolizidine has been developed based on a diastereofacially selective cycloaddition of dichloroketene with a chiral dienol ether.