111964-19-3

Upstream product

• 693-03-8 n-butyl magnesium bromide 
• 111964-18-2 (3R,5S,7aS)-5-Heptyl-3-phenyl-hexahydro-pyrrolo[2,1-b]oxazole 
• 56613-80-0 D-2-phenylglycinol 
• 111980-33-7 (-)-N-cyanomethylphenylglycinol 
• 195299-15-1 2-cyano-5-oxazolopyrrolidine 
• 111964-17-1 (3R,7aS)-5-Heptyl-3-phenyl-hexahydro-pyrrolo[2,1-b]oxazole-5-carbonitrile 

Downstream Products

• 112020-14-1 (+)-(S)-trans-2-heptyl-5-butyl-1-benzyl pyrrolidine 
• 111964-20-6 (S)-1-((2S,5S)-2-Butyl-5-heptyl-pyrrolidin-1-yl)-3,3,3-trifluoro-2-methoxy-2-phenyl-propan-1-one 
• 105147-76-0 ((2S,5S)-2-Butyl-5-heptyl-pyrrolidin-1-yl)-phenyl-methanone 
• 95587-14-7 (+)-(S)-trans-2-heptyl-5-butylpyrrolidine 

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

ASYMMETRIC SYNTHESIS X : A CHIRAL PYRROLIDINE SYNTHON FOR A NEW APPROACH TO THE SYNTHESIS OF ALKALOIDS

The synthesis of chiral 2-cyano-5-oxazolopyrrolidine 3 is reported.The synthesis of the optically pure ant venom alkaloid, (+)-(S)-trans-2-heptyl-5-butyl-pyrrolidine 7, has been achieved from 3.