52481-82-0Relevant articles and documents
Trimethylphosphine-Promoted Alcoholysis of α,β-Unsaturated Imides and α,β-Unsaturated Esters
Sato, Haruka,Hosokawa, Seijiro
, p. 1343 - 1349 (2018/01/27)
α,β-Unsaturated imides and α,β-unsaturated esters were found to undergo alcoholysis in the presence of trimethylphosphine. The reaction is initiated by nucleophilic addition of trimethylphosphine to the double bond of the α,β-unsaturated carbonyl compound. Saturated imides also undergo the alcoholysis in the presence of the corresponding α,β-unsaturated imide.
N-Phosphoryl oxazolidinones as effective phosphorylating agents
Jones, Simon,Smanmoo, Chaiwat
, p. 1585 - 1588 (2007/10/03)
A number of N-phosphoryl oxazolidinones have been prepared and evaluated, the best being 5,5-diphenyl oxazolidinones, the utility of which was demonstrated in the phosphorylation of a number of representative primary, secondary, tertiary, and phenolic alcohols.
1,3-Oxazolidin-2-ones from 1H-Aziridines by a Novel Stratagem which Mimics the Direct Insertion of CO2
Banks, Malcolm R.,Cadogan, J. I. G.,Gosney, Ian,Hodgson, Philip K. G.,Thomson, Dian E.
, p. 961 - 962 (2007/10/02)
N-Ethoxycarbonylaziridines 2 undergo smooth thermal transformation into 1,3-oxazolidin-2-ones 3 on flash pyrolysis by a tandem reaction sequence equivalent to direct insertion of CO2 into the parent 1H-aziridine.