422507-07-1

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 162338-03-6 N-benzyl-trans-4-aminocyclohexanol 
• 188562-91-6 tert-butyl N-benzyl(4-oxocyclohexyl)carbamate 

Downstream Products

• 422507-09-3 4-[N-benzyl-N-(tert-butoxycarbonyl)amino]cyclohex-1-ene 
• 1204401-30-8 tert-butyl benzyl(cis-4-iodocyclohexyl)carbamate 
• 187807-24-5 4-{benzyl-[2-(methylselanyl)-2-oxoethyl]amino}cyclohex-1-ene 
• 422507-12-8 4-[N-benzyl-N-(methoxycarbonylmethyl)amino]-1-cyclohexene 
• 187807-23-4 N-benzyl-N-(3-cyclohexenyl)amine 

Relevant academic research and scientific papers

A simple and efficient synthesis of N-substituted cyclohex-3-enamines

A straightforward preparation of N-substituted cyclohex-3-enamines starting from the commercially available trans-4-aminocyclohexanol hydrochloride is described. Cyclohex-3-enamino-functionalized compounds have proven to be interesting intermediates in me

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.