Affiliation:
1. Vorozhtsov Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences (NIOCH SB RAS)
Abstract
A new method for the synthesis of 5,5-disubstituted N-methyl-1,3-oxazinanes as a mixture of diastereomers at position 5 containing monoterpene and branched alkyl substituents at position 5 has been developed. The 1,3-oxazinanes were obtained for the first time by the interaction of 2,2-substituted 3-aminopropane-1-ols with formaldehyde and sodium borohydrides in a single stage.
Publisher
The Russian Academy of Sciences