Hidroxi-fenolok szelektív foszforilezése és foszfinilezése

Translated title of the contribution: Study on the selective phosphorylation and phosphinylation of hydroxyphenols

Andrea Toldy, György Keglevich, György Marosi, Péter Anna, Gyula Parlagh, Zoltán Nagy, Krisztina Ludányi

Research output: Contribution to journalArticle

Abstract

Choosing appropriate reaction conditions, the phosphorylation of hydroquinone by diethyl chlorophosphate gave predominantly the monophosphate (2). A similar reaction of phloroglucinol led to a mixture of the three possible products (6, 7 and 8). The monophosphinylation of the above hydroxyphenols by diphenylphosphinyl chloride could be accomplished with a good selectivity to give monophosphinates (4 or 9) in variable yields.

Original languageHungarian
Pages (from-to)543-546
Number of pages4
JournalMagyar Kemiai Folyoirat, Kemiai Kozlemenyek
Volume108
Issue number12
Publication statusPublished - Dec 2002

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Phloroglucinol
Phosphorylation
Chlorides
hydroquinone
diethylchlorophosphate

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Hidroxi-fenolok szelektív foszforilezése és foszfinilezése. / Toldy, Andrea; Keglevich, György; Marosi, György; Anna, Péter; Parlagh, Gyula; Nagy, Zoltán; Ludányi, Krisztina.

In: Magyar Kemiai Folyoirat, Kemiai Kozlemenyek, Vol. 108, No. 12, 12.2002, p. 543-546.

Research output: Contribution to journalArticle

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AU - Anna, Péter

AU - Parlagh, Gyula

AU - Nagy, Zoltán

AU - Ludányi, Krisztina

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