28819-40-1Relevant academic research and scientific papers
The synthesis of new 1,3-oxazolidines and 1,3-oxazinanes containing (η6-arene)tricarbonylchromium group based on condensation between aldehydes and amino alcohols
Artemov,Sazonova,Krylova,Zvereva,Pechen,Fukin,Cherkasov,Faerman,Grishina, N. Yu.
, p. 884 - 892 (2018/08/28)
The condensation reactions of β- and γ-amino alcohols containing phenyl or (η6-arene) tricarbonylchromium substituent with formaldehyde, acetaldehyde, benzaldehyde, and (η6-benzaldehyde)tricarbonylchromium were studied. The resulting 1,3-oxazolidine and 1,3-oxazinane products were isolated in a pure form and identified by different physicochemical methods. The effect of (η6-arene)tricarbonylchromium moiety on the reaction process was demonstrated.
Electrochemical Oxidation of 1-Phenylpyrazolidin-3-ones. Part 1. 4- and 5-Substituted 1-Phenylpyrazolidin-3-ones
Bellamy, Anthony J.,Innes, David I.,Hillson, Peter J.
, p. 1599 - 1604 (2007/10/02)
The electrochemical oxidation of 4-methyl-, 5-phenyl-, and 4-hydroxymethyl-4-methyl-1-phenylpyrazolidin-3-one in acetonitrile has been studied.All three systems behave in a manner similar to that of the parent 1-phenylpyrazolidin-3-one, the major reaction
