33578-23-3Relevant articles and documents
Silver-Catalyzed Oxyphosphorylation of Unactivated Alkynes
Liu, Binbin,Song, Qingmin,Liu, Zhaohong,Wang, Zikun
supporting information, p. 3214 - 3219 (2021/05/27)
Here, we describe an application of hydroazidation in the instant activation of alkynes for achieving the oxyphosphorylation of unactivated alkynes with diarylphosphinoyl radicals under mild reaction conditions. This reaction provides a method for accessing β-ketophosphine oxides and phosphorus-containing pyrroles. (Figure presented.).
Copper catalyzed one-pot synthesis of β-ketophosphine oxides from ketones and H-phosphine oxides
Zhang, Zhi-Jie,Yi, Dong,Fu, Qiang,Liang, Wu,Chen, Su-Yuan,Yang, Lu,Du, Feng-Tian,Ji, Jian-Xin,Wei, Wei
supporting information, p. 2417 - 2420 (2017/06/01)
A facile and efficient copper catalyzed one-pot method has been developed for the formation of β-ketophosphine oxides from ketones and H-phosphine oxides under air at room temperature, in which vinylhydrazinedicarboxylate was formed as the key intermediate. Preliminary mechanistic studies indicated that the reaction might involve a radical process and carbonyl oxygen atom of β-ketophosphine oxides came from molecular oxygen.
Reactions of Anions from α-Diphenylphosphinoyl Ketones with Electrophiles
Torr, Richard S.,Warren, Stuart
, p. 1173 - 1180 (2007/10/02)
Anions from α-Ph2P(O)-ketones do not give Horner-Wittig reactions but do react with alkyl halides, including α-halogenocarbonyl compounds, and Michael acceptors.The products may be stereoselectively reduced.