77643-59-5

Upstream product

• 37854-15-2 2-bromo-3-phenyl-2-propenenitrile 
• 75-64-9 tert-butylamine 
• 19521-13-2 α,β-dibromo-β-phenylpropionitrile 
• 935-02-4 3-Phenyl-2-propynonitrile 

Relevant academic research and scientific papers

A novel strategy for the synthesis of 2,6-diaryl-1,2-dihydropyridines via 6π-electrocyclization

Enaminonitriles with α,β-unsaturated aldehydes in a BF 3·OEt2 catalyzed reaction gave stable 1-azatrienes, which could be readily transformed to 1,2-dihydropyridines via 1,6-electrocyclizations.

Addition de cyano-2 aziridines a quelques alcynes; obtention de pyrroles

Addition of the α-bromocinnamonitrile to primary amines (Cromwell method) leads to 2-cyano-3-phenyl-N-alkyl-aziridines, but the formation of the isomeric enamines always competes with this reaction.These aziridines, which are potential azomethine-ylids, a