16114-84-4Relevant academic research and scientific papers
Controllable phosphorylation of thioesters: Selective synthesis of aryl and benzyl phosphoryl compounds
Xu, Kaiqiang,Liu, Long,Li, Zhaohui,Huang, Tianzeng,Xiang, Kang,Chen, Tieqiao
, p. 14653 - 14663 (2020/12/29)
The controllable phosphorylations of thioesters were developed. When the reaction was catalyzed by a palladium catalyst, aryl or alkenyl phosphoryl compounds were generated through decarbonylative coupling, while the benzyl phosphoryl compounds were produced through deoxygenative coupling when the reaction was carried out in the presence of only a base.
Sigmatropic isomerizations in azaallyl systems: XX. N- Alkylbenzimidoylphosphonates
Onys'ko,Kim,Rassukanaya,Kiseleva,Sinitsa
, p. 1341 - 1349 (2007/10/03)
Synthetic approaches are developed to benzimidoylphosphoryl derivatives containing electronically and sterically diverse alkyl substituents on the nitrogen atom, as well as their prototropic isomers. Regularities in prototropic transitions in the phosphorylated C=N-C triad were revealed and applied in the synthesis of α-aminophosphonic acid derivatives. 2004 MAIK "Nauka/Interperiodica".
TERTIAERE PHOSPHINOXIDE AUS DIPHENYLCHLORPHOSPHIN UND CARBONSAEUREN
Sartori, Peter,Mosler, Gerhard
, p. 115 - 120 (2007/10/02)
Starting from Diphenylchlorophosphine and mono or dicarboxylic acids, the preparation of diphenylalkylphosphine oxides, in good yields in a simple synthetic procedure is described.
