1225012-70-3

Upstream product

• 6630-33-7 ortho-bromobenzaldehyde 
• 351980-24-0 N'-(2-bromobenzylidene)benzohydrazide 
• 1224945-35-0 (S,E)-N-benzylidene-1-(2-bromophenyl)but-3-en-1-amine 
• 910545-65-2 (1R,3R,4S)-3-allyl-3-amino-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 

Downstream Products

• 1224945-34-9 (S)-1-(2-bromophenyl)but-3-en-1-amine hydrochloride 
• 1392047-84-5 (2S)-2-(2-bromophenyl)-1,2,3,6-tetrahydropyridine 
• 1392047-99-2 (S)-5,6-dihydro-6-(2-bromophenyl)pyridin-2(1H)-one 
• 1392047-77-6 C₁₃H₁₆BrN 
• 1392047-91-4 C₁₃H₁₄BrNO 

Relevant academic research and scientific papers

Asymmetric synthesis of highly enantioenriched 2-substituted piperidines and 6-substituted piperidine-2-ones by a combination enantioselective hydrazone allylation with ring closing metathesis

An efficient method for the asymmetric synthesis of highly optically pure 2-substituted piperidines and 6-substituted piperidine-2-ones from aldehydes was developed by a sequence of enantioselective hydrazone allylation and ring closing metathesis. This m

( PYRROLIDIN-2 -YL) PHENYL DERIVATIVES FOR USE IN THE TREATMENT OF PAIN

The invention relates to (pyrrolidin-2-yl)phenyl derivatives having the general Formula (I), wherein R1 is (C1-4)alkyl, halo(C1-4)alkyl, (C1-4)alkyloxy, or halo(C1-4)alkyloxy; R2 is H, (Cs

(PYRROLIDIN-2-YL)PHENYL DERIVATIVES

The invention relates to (pyrrolidin-2-yl)phenyl derivatives having the general Formula I wherein R1 is (C1-4)alkyl, halo(C1-4)alkyl, (C1-4)alkyloxy, or halo(C1-4)alkyloxy; R2 is H, (C