Synthesis and study of the structure of new N-substituted 2-methyl-5-(1-methylethyl) cyclohexylamines
作者:I. I. Bardyshev、N. G. Kozlov、T. K. Vyalimyaé、T. I. Pekhk
DOI:10.1007/bf00568377
日期:1980.7
(+)-S-carvone with aliphatic nitriles and the hydroamination of some aldehydes and ketones with (+)-S-carvone oxime have been developed. The optimum conditions for performing these processes has been selected. It has been established by13C NMR that the reactions studied form a mixture of N-substituted carvo-, isocarvo-, neocarvo-, and neoisocarvomenthylamines in a ratio of 65:20:10:5. As a result of