422507-48-0

Upstream product

• 422507-45-7 4-benzylamino-1-trimethylsilyloxycyclohexane-1-carbonitrile 
• 7677-24-9 trimethylsilyl cyanide 
• 188562-91-6 tert-butyl N-benzyl(4-oxocyclohexyl)carbamate 

Downstream Products

• 1610517-29-7 ethyl 3-[benzyl(4-cyanocyclohex-3-en-1-yl)amino]-2,2-dichloro-3-oxopropanoate 
• 422507-39-9 4-{N-benzyl-N-[2-(phenylselanyl)-2-oxoethyl]amino}cyclohex-1-enecarbonitrile 
• 187807-27-8 4-{N-benzyl-N-[3-(methylselanyl)-3-oxopropyl]aminocyclohex}-1-enecarbonitrile 
• 422507-26-4 4-[N-benzyl-N-(2-methoxycarbonylethyl)amino]-1-cyclohexenecarbonitrile 
• 422506-79-4 4-[N-benzyl-N-(methoxycarbonylmethyl)amino]cyclohex-1-enecarbonitrile 
• 187807-20-1 4-{N-benzyl-N-[2-(methylselanyl)-2-oxoethyl]amino}cyclohex-1-enecarbonitrile 
• 187807-19-8 4-(benzylamino)cyclohex-1-encarbonitrile 

Relevant academic research and scientific papers

Chlorine atom transfer radical 6-exo cyclizations of carbamoyldichloroacetate-tethered alkenes, enol acetates and α,β-unsaturated nitriles leading to morphans

The CuI-mediated atom transfer radical cyclization of amino-tethered dichloromalonamides and electron-rich, electron-poor, and nonactivated double bonds is a useful methodology for the synthesis of 2-azabicyclo[3.3.1]nonanes. A study of the rea

Decarbonylative radical cyclization of α-amino selenoesters upon electrophilic alkenes. A general method for the 6-azabicyclo[3.2.1]octane synthesis

α-Amino selenoester-tethered electronically poor alkenes on treatment with tributyltin hydride or TTMSS undergo intramolecular radical cyclization to provide 6-azabicyclo[3.2.1]octanes through 1-aminomethyl radical intermediates.