81583-86-0

Upstream product

• 81583-85-9 N-(4-tert-butylcyclohexylidene)-1-phenylethylamine 
• 618-36-0 rac-methylbenzylamine 
• 81583-85-9 (4-tert-Butyl-cyclohexylidene)-((S)-1-phenyl-ethyl)-amine 
• 98-53-3 4-tercbutyl-cyclohexanone 
• 2627-86-3 (S)-1-phenyl-ethylamine 
• 81583-85-9 (-)-(S)-N-(4-tert-butylcyclohexylidene)-α-methylbenzylamine 

Downstream Products

• 126785-64-6 (R)-5-tert-Butyl-1-((R)-1-phenyl-ethyl)-azepan-2-one 
• 81583-87-1 (S)-5-tert-Butyl-1-((R)-1-phenyl-ethyl)-azepan-2-one 
• 81583-87-1 (R)-5-tert-Butyl-1-((S)-1-phenyl-ethyl)-azepan-2-one 
• 81583-87-1 (5S,αS)-5-tert-butyl-1-(α-methylbenzyl)hexahydro-2-azepinone 

Relevant academic research and scientific papers

SELECTIVITY IN AN ASYMMETRIC NITROGEN INSERTION PROCESS

A simple and efficient synthesis of chiral lactams utilizing a group-selective nitrogen insertion process has been investigated for a group of prochiral ketones.The preparation of a useful intermediate in benzomorphinan synthesis has been carried out in o

Photochemical and Thermal Rearrangement of Oxaziridines. Experimental Evidence in Support of the Stereoelectronic Control Theory

The irradiation of an optically pure isomer of a spirooxaziridine, (2R,αS)-6(e)-tert-butyl-2-(α-methylbenzyl)-1,2-oxazaspirooctane, gave a single lactam, (5S,αS)-5-tert-butyl-1-(α-methylbenzyl)hexahydro-2-azepinone.The absolute configurations of thes