Abstract
The tertiary polyfunctional triphosphine sulfides with amino and (or) ether groups have been synthesized in excellent yields by the exhaustive regioselective (in anti-Markovnikov manner) addition of secondary phosphines sulfides to trivinyl ethers of aminotriols and triols under free-radical conditions (UV-irradiation, 1.5–5 h).
GRAPHICAL ABSTRACT
Funding
This work was supported by the President of the Russian Federation [program for the support of leading scientific schools, grant NSh-156.2014.3].
Disclosure statement
No potential conflict of interest was reported by the authors.