348608-06-0

Upstream product

• 27482-95-7 (R)-N-(n-propylmethylidene)-1-methylbenzylamine 
• 106-95-6 allyl bromide 
• 348608-03-7 (+)-N-[(R)-α-methylbenzyl]-hept-1-ene-4-amine 

Downstream Products

• 348608-12-8 2R-(+)-4,5-didehydro-N-[(R)-α-methylbenzyl]-2-propyl-piperidine 

Relevant academic research and scientific papers

Synthesis of (-)-coniine and (-)-pipecoline using ruthenium catalyzed ring closing metathesis

Ring closing metathesis employing the well-known Grabbs' ruthenium catalyst has been used as the key step in the synthesis of piperidine alkaloids, (-)-coniine and (-)-pipecoline, and the asymmetric induction has been performed by using (R)-α-methyl benzy