62854-15-3

Upstream product

• 100379-91-7 (+/-)-N-(3t-bromo-2c-hydroxy-cyclohex-r-yl)-benzamide 
• 4654-36-8 (RS)-N-(cyclohex-2-en-1-yl)benzamide 
• 22613-33-8 2-cyclohexenylamine hydrochloride 
• 98-88-4 benzoyl chloride 
• 103798-44-3 (+/-)-7c-bromo-2-phenyl-(3ar,7ac)-3a,4,5,6,7,7a-hexahydro-benzoxazole 
• 1541-25-9 3-amino-1-cyclohexene 

Relevant academic research and scientific papers

cis- and trans-Stereoselective Epoxidation of N-Protected 2-Cyclohexen-1-ylamines

(Equation Presented) The first systematic study of the cis and trans stereoselectivity in the m-CPBA epoxidation of N-protected cyclic allylic amines has been completed. Mono-N-protected systems gave epoxides with cis stereochemistry (amides are better ci

Diastereoselectivity in the epoxidation of substituted cyclohexenes by dimethyldioxirane

Three series of compounds based on the cyclohexene framework have been epoxidized by dimetbyldioxirane. A pronounced dependence of epoxide diastereoselectivity on substituent has been observed. In addition there is a solvent influence on this stereoselectivity. The results have been explained by invoking steric, H-bonding, and dipole - dipole influences on the epoxide stereochemistry.