105147-76-0

Upstream product

• 111964-17-1 (3R,7aS)-5-Heptyl-3-phenyl-hexahydro-pyrrolo[2,1-b]oxazole-5-carbonitrile 
• 112020-15-2 (R)-2-((2R,5S)-2-Butyl-5-heptyl-pyrrolidin-1-yl)-2-phenyl-ethanol 
• 111964-18-2 (3R,5S,7aS)-5-Heptyl-3-phenyl-hexahydro-pyrrolo[2,1-b]oxazole 
• 95587-05-6 cis-2-heptyl-5-butylpyrrolidine 
• 98-88-4 benzoyl chloride 
• 105147-77-1 1-((3aR,6R)-2-Vinyl-hexahydro-pyrrolo[1,2-b]isoxazol-6-yl)-heptan-2-ol 
• 105147-71-5 1-((R)-1-Oxy-3,4-dihydro-2H-pyrrol-2-yl)-heptan-2-ol 
• 105147-72-6 1-((2S,3aR,6R)-2-Ethyl-hexahydro-pyrrolo[1,2-b]isoxazol-6-yl)-heptan-2-ol 
• 105147-73-7 1-[(2R,5R)-5-(2-Hydroxy-butyl)-pyrrolidin-2-yl]-heptan-2-ol 
• 105147-70-4 (2R,3aR)-2-Pentyl-hexahydro-pyrrolo[1,2-b]isoxazole 
• 592-76-7 1-Heptene 
• 111964-19-3 (R)-2-((2S,5S)-2-Butyl-5-heptyl-pyrrolidin-1-yl)-2-phenyl-ethanol 
• 95587-14-7 (+)-(S)-trans-2-heptyl-5-butylpyrrolidine 

Downstream Products

• 112020-14-1 (+)-(S)-trans-2-heptyl-5-butyl-1-benzyl pyrrolidine 
• 105147-82-8 (2S,5R)-1-Benzyl-2-butyl-5-heptyl-pyrrolidine 

Relevant academic research and scientific papers

ASYMMETRIC SYNTHESIS XII: STEREOCONTROLLED ELECTROPHILIC-NUCLEOPHILIC α,α'-SUBSTITUTION OF THE PYRROLIDINE RING.

The synthesis of 2-cyano-5-oxazolopyrrolidine 3, a chiral pyrrolidine synthon, is described.Conditions were established that permitted sequential chemoselective reactions at the C-2 aminonitrile (electrophilic substitution) and at the C-5 aminoether (nucl

THE α,α'-DIALKYLATION OF CYCLIC AMINES. THE SYNTHESIS OF SOLENOPSIS ANT VENOMS.

A trans-α,α'-dialkylation of cyclic amines has been investigated through the use of nitrone methodology.This procedure has been utilized in the synthesis of Solenopsis ant venoms.