141394-46-9

Upstream product

• 59707-13-0 2-allylmalononitrile 

Downstream Products

• 141314-65-0 (2,3-trans)-(3,4-cis)-1,1-dicyano-2,4-dimethyl-3-phenyl-cyclopentane 
• 141314-64-9 (1,4-trans)-(2,3-trans)-(3,4-cis)-1-cyano-4-cyanomethyl-2-methyl-3-phenyl-cyclopentane 
• 141314-64-9 (1,4-cis)-(2,3-trans)-(3,4-cis)-1-cyano-4-cyanomethyl-2-methyl-3-phenyl-cyclopentane 
• 141314-65-0 (2,3-trans)-(3,4-trans)-1,1-dicyano-2,4-dimethyl-3-phenyl-cyclopentane 
• 141314-64-9 (1,4-cis)-(2,3-trans)-(3,4-trans)-1-cyano-4-cyanomethyl-2-methyl-3-phenyl-cyclopentane 
• 141314-64-9 (1,4-trans)-(2,3-trans)-(3,4-trans)-1-cyano-4-cyanomethyl-2-methyl-3-phenyl-cyclopentane 

Relevant academic research and scientific papers

Radical Annulation Reactions of Allyl Iodomalononitriles

Heating of allyl iodomalononitriles with alkenes, followed by tin hydride reduction, forms 1-(cyanoalkyl)-4-cyanocyclopentane rings with up to 5 new stereocenters by a sequence of atom transfer addition followed by nitrile transfer cyclization. Key words: