76403-31-1

Upstream product

• 67-56-1 methanol 
• 76403-14-0 (1-Isocyanato-but-3-enyl)-benzene 
• 122716-70-5 (α-methoxy-benzyl)-carbamic acid methyl ester 
• 106-95-6 allyl bromide 
• 426825-64-1 (4-methoxy-phenyl)-(1-phenyl-but-3-enyl)-carbamic acid methyl ester 
• 100-52-7 benzaldehyde 
• 150562-30-4 4-methoxy-N-(1-phenylbut-3-enyl)aniline 

Downstream Products

• 76403-37-7 (4-Hydroxy-1-phenyl-butyl)-carbamic acid methyl ester 
• 4383-23-7 1-phenyl-but-3-enylamine 
• 22050-10-8 (+/-)-5-phenyl-2-pyrrolidinone 
• 76403-42-4 2-Oxo-5-phenyl-pyrrolidine-1-carboxylic acid methyl ester 

Relevant academic research and scientific papers

Three component synthesis of homoallylic amines. Efficient catalysis by lanthanum triflate/benzoic acid

Lanthanum triflate-benzoic acid catalyses the in situ formation and allylation of various imines from aldehydes and an aromatic amine.

Reaction of N-Acyl-α-methoxyamines with Organozic Reagents. A Convenient Method for the Synthesis of Homoallylamines and β-Amino Esters.

The reaction of N-acyl-α-methoxyamines with allyl-, propargyl-, and benzylzinc bromides and Reformatsky reagents proceeds in THF at room temperature.Homoallyl- and homopropargylamines and β-amino esters are synthesized in good yields.

An Efficient and General Synthesis of 5-Substituted Pyrrolidinones

2-Pyrrolidinone derivatives are widespread materials of considerable laboratory and commercial importance.In spite of this, there is no generally useful synthesis of either symmetrically or unsymmetrically 5,5-disubstituted derivatives.This is particularl