62114-59-4

Upstream product

• 5292-53-5 diethyl benzalmalonate 
• 106-95-6 allyl bromide 
• 1730-25-2 allylmagnesium bromide 
• 100-52-7 benzaldehyde 
• 105-53-3 diethyl malonate 

Downstream Products

• 63473-86-9 phenyl-3 hexene-5 oate d'ethyle 
• 62152-81-2 2-(1-Phenyl-but-3-enyl)-malonic acid 
• 62114-70-9 chloromethyl-2 methyl-1 phenyl-4 piperidine 
• 52129-49-4 3-phenylhex-5-enoic acid 
• 65559-66-2 N-methyl-3-phenyl-5-hexenamide 
• 62114-62-9 N-methyl phenyl-3 hexene-5 yl amine 
• 65559-67-3 N-chloro N-methyl phenyl-3 hexene-5 yl amine 
• 62114-64-1 N,N-dimethyl phenyl-3 hexene-5 yl amine 
• 62114-65-2 N-allyl N-methyl phenyl-3 hexene-5 yl amine 
• 62114-71-0 methoxymethyl-2 methyl-1 phenyl-4 piperidine 
• 62114-66-3 N-benzyl N-methyl phenyl-3 hexene-5 yl amine 
• 80534-97-0 methyl-1 piperidinomethyl-2 phenyl-4 piperidine 
• 80534-95-8 N-methyl phenyl-3 hexene-5 yl trifluoroacetamide 
• 80534-96-9 N-methyl epoxy-5,6 phenyl-3 hexyl trifluoroacetamide 

Relevant academic research and scientific papers

Regioselective allylation and alkylation of electron-deficient alkenes with organogallium and organoindium reagents

Triorganogallium and -indium reagents reacted with α,β-unsaturated nitrile and carbonyl compounds to give 1,4-addition products regioselectively. The reaction of allylgallium and allylindium sesquihalides with α,β-unsaturated carbonyl compounds proceeded

SYNTHESE RADICALAIRE D'ANALGESIQUES POTENTIELS: ARYL-4 PIPERIDINES SUBSTITUEES EN 2 ET BENZOMORPHANES

The synthesis of a series of 3-aryl 5-hexenyl amines and the cyclisations of the corresponding N-chloroamines are described.When the ring closure results from the amino radical addition to the ethylenic double bond, 2-chloromethyl 4-phenyl piperidines are obtained.These compounds lead by intramolecular Friedel-Crafts reaction to varied substituted 6,7-benzomorphanes.When the phenyl ring is substituted with a methoxyl group, the cyclisation proceeds via homolytic aromatic substitution and 4-allyl tetrahydroquinolines are formed.