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Reactions of nitroxides, part XI: O ‐Aryl phenylselenophosphonates bearing a nitroxyl moiety by Bogumiła Huras; Jerzy Zakrzewski; Maria Krawczyk is a Chemistry article available to read on EtoBox.
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## Abstract __O__‐Aryl phenylselenophosphonates bearing a nitroxyl moiety were synthesized in the presence of pyridine in diethyl ether from 4‐hydroxy‐2,2,6,6‐tetramethylpiperidine‐1‐oxyl, and either phenyldichlorophosphine and elemental selenium in 9–35% yield or phenyldichlorophosphine selenide in 36–62% yield. __O__,__O__‐Diaryl phenylselenophosphonates and __O__,__O__‐bis(2,2,6,6‐tetramethyl‐1‐oxyl‐4‐piperidyl)phenylselenophosphonates were obtained as by‐products. __O__,__O__‐Diaryl phenylselenophosphonates were obtained from phenyldichlorophosphine selenide and 2 mol of phenols in 55–86% yield. Antifungal activity of some synthesized selenophosphonates was found. © 2011 Wiley Periodicals, Inc. Heteroatom Chem 22:137–147, 2011; View this article online at wileyonlinelibrary.com. DOI 10.1002/hc.20667
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- Author
- Bogumiła Huras; Jerzy Zakrzewski; Maria Krawczyk
- Publisher
- John Wiley and Sons; Hindawi Limited; John Wiley & Sons Inc.; Wiley (ISSN 1042-7163)
- Published
- 2011
- Language
- EN
- Field
- Chemistry (Physical Sciences)
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