17435-60-8Relevant academic research and scientific papers
Determination of the conformations and relative configurations of exocyclic amines
Montalvo-gonzlez, J. Ascencin,Iniestra-galindo, Maria Guadalupe,Ariza-castolo, Armando
, p. 938 - 944 (2011/07/30)
The conformations and relative configurations of 20 amines, classified according to the following labeling scheme, were analyzed. Series a comprised compounds derived from N-(1-phenylethyl)cyclohexanamine, b comprised derivatives of N-[1-(naphthalen-2-yl)ethyl]cyclohexanamine, c comprised derivatives of N-(diphenylmethyl)cyclohexanamine, and d comprised derivatives of N-(propan-2-yl)cyclohexanamine. The compounds were labeled as follows: 1 indicates cyclohexanamine, 2 indicates 2-methylcyclohexanamines, 3 indicates 3-methylcyclohexanamines, 4 indicates 4-methylcyclohexanamines, and 5 indicates 4-tert-butylcyclohexanamines. These compounds were prepared without the use of stereoselective induction and, therefore, all expected stereoisomers were observed. Structural assignments were established by 1H, 13C, and 15N NMR.
Reductive Amination of Ketones and Aldehydes at the Mercury-Cathode
Pienemann, Thomas,Schaefer, Hans-J.
, p. 1005 - 1007 (2007/10/02)
Secondary amines are prepared in good yields by potential-controlled reduction of aldehydes or ketones at a mercury cathode in an aqueous solution containing a primary amine.For cyclic ketones, high diastereoselectivities are obtained in some cases.
