1,2-hydrogen Migration in Aminoalkyl Radicals
Year: 2016
Type: article
Abstract: The amination reaction of α-olefins C4-C7 in the oxidation-reduction system NН2OH∙HCl-TiCl3 has been investigated; as a result the mono- and diamines of various structures have been prepared. It has been found that in attack of -radical to olefin it takes place a hydrogen migration from first carbon to second one. It has been shown that in composition of the reaction products besides purposeful individual amines there are detected telomers, the molecular masses of which are changed approximately within the ranges of, Мn = 460-800.
Source: European Chemical Bulletin
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: bronze
OpenAlex ID: W2592837320
