860032-69-5Relevant academic research and scientific papers
Chemistry of phosphorus ylides. Part 25 [1]. Interaction of hexaphenylcarbodiphosphorane with carbonyls, hydrazone, and Mannich bases. A synthesis of phosphoranylidenes, phosphobetaines, and oxaphosphinin
Said, Medhat M.,Maigali, Soher S.,Abd-El-Maksoud, Mansoura A.,Soliman, Fouad M.
experimental part, p. 1299 - 1306 (2009/12/05)
The reaction of the allylic hexaphenylcarbodiphosphorane with carbonyls afforded the corresponding phosphoranylidene derivatives. On the other hand, the stable phosphorbetaines were obtained when the bisphosphorane was allowed to react with the α-diketone and triketone. The azaphosphoranylidene was isolated from the reaction of the bisphosphorane with hydrazone. Moreover, the bisphosphorane reacted with niclosamide and quinoline Mannich bases with the formation of the oxaphosphinins. When the Wittig reaction was performed with the new phosphoranes, the corresponding exocyclic olefins were obtained. On the other hand, the oxaphosphinins were produced when the phosphoranes were treated under the condition of a Hoffmann degradation reaction.
Chemistry of phosphorus ylides. Part 22 [1]. Effect of newly synthesized niclosamide Mannich bases, phosphopyranones, phosphoranylidenes, and oxaphosphinin on some metabolic aspects of Biomphalaria alexandrina
Soliman, Fouad M.,Said, Medhat M.,Maigali, Soher S.
, p. 241 - 251 (2007/10/03)
Niclosamide reacts with secondary amines and formaldehyde under the condition of Mannich reaction, to give new Mannich bases. The reaction of these niclosamide Mannich bases with active phosphacumulene ylides affords the corresponding phenyliminopyranone,
