Hydro-de-phosphoniation of 4-substituted-4-triphenylphosphonio-5(4H)-oxazolones with hydrogen iodide

Article abstract of DOI:10.1080/10426509908037030

4-Substituted-4-triphenylphosphonio-5(4H)-oxazolones, when reacted with hydrogen iodide in methylene chloride at room temperature, undergo hydro-de-phosphoniation to 5(4H)-oxazolonium salts, which react with methanol and triethylamine to give the correspo

Full text of DOI:10.1080/10426509908037030

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Phosphorus, Sulfur, and Silicon
and the Related Elements
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HYDRO-DE-PHOSPHONIATION
OF 4-SUBSTITUTED-4-
TRIPHENYLPHOSPHONIO-S(4H)-
OXAZOLONES WITH HYDROGEN
IODIDE
a b
a
Roman Mazurkiewicz , Anna W. Pierwocha
&
a
Agata Zabska
a
Institute of Organic Chemistry and Technology,
The Silesian Technical University , Krzywoustego 4,
4
4-100, Gliwice, Poland
b
Department of Textile Engineering and
Environmental Sciences , Technical University of
Lodz , Bielsko-Biala Campus, 43-300, Bielsko-Biala,
Poland
Published online: 24 Sep 2006.
To cite this article: Roman Mazurkiewicz , Anna W. Pierwocha & Agata Zabska (1999)
HYDRO-DE-PHOSPHONIATION OF 4-SUBSTITUTED-4-TRIPHENYLPHOSPHONIO-S(4H)-
OXAZOLONES WITH HYDROGEN IODIDE, Phosphorus, Sulfur, and Silicon and the Related
Elements, 149:1, 167-178, DOI: 10.1080/10426509908037030
To link to this article: http://dx.doi.org/10.1080/10426509908037030
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