Generation of tert-Butyl-λ5-phosphanedione and Its Chemical Properties


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Abstract

Flash vacuum thermolysis of trimethylsilyl tert-butylphosphonohalidates involved elimination of halo(trimethyl)silane with the formation of tert-butyl-λ5-phosphanedione whose structure was confirmed by chemical reactions. tert-Butyl-λ5-phosphanedione readily undergoes trimerization, reacts with 2-phenyloxirane to give cycloaddition product, and takes up alcohols.

About the authors

O. I. Kolodyazhnyi

Institute of Bioorganic and Petroleum Chemistry

Author for correspondence.
Email: olegkol321@gmail.com
Ukraine, ul. Murmanskaya 1, Kiev, 02094

E. V. Grishkun

Institute of Bioorganic and Petroleum Chemistry

Email: olegkol321@gmail.com
Ukraine, ul. Murmanskaya 1, Kiev, 02094

A. O. Kolodyazhnaya

Institute of Bioorganic and Petroleum Chemistry

Email: olegkol321@gmail.com
Ukraine, ul. Murmanskaya 1, Kiev, 02094

O. O. Kolodyazhna

Institute of Bioorganic and Petroleum Chemistry

Email: olegkol321@gmail.com
Ukraine, ul. Murmanskaya 1, Kiev, 02094

S. Yu. Sheiko

Institute of Bioorganic and Petroleum Chemistry

Email: olegkol321@gmail.com
Ukraine, ul. Murmanskaya 1, Kiev, 02094

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