103988-85-8Relevant articles and documents
SUBSTITUTION OF 3H-FURAN-2-ONES IN AMINATION AND HYDROAMINATION REACTIONS
Morozova, N. A.,Sedavkina, V. A.,Egorova, A. Yu.
, p. 308 - 311 (1994)
The amination and hydroamination of 5-alkyl-3H-furan-2-ones and their 3-benzylidene- and 3-formyl-derivatives were studied.The characteristics of the reactions, the requirements for the nature of the nucleophilic reagents, and the reaction conditions leading to the destruction of the furan ring and recyclization to pyrrolidinone and pyrrolinone structures are indicated.
Heterocyclization of derivatives of 4-oxoalkanoic acids to 1,5-disubstituted pyrrolin-2-ones
Egorova,Sedavkina,Timofeeva
, p. 694 - 697 (2007/10/03)
Conditions were developed for the synthesis and production of 1-aryl-5-alkyl(aryl)-3H- and 1-aryl-5-alkyl(aryl)-5H-pyrrolin-2-ones from the amides and esters of 4-oxoalkanoic acids. It was established that the yield and ratio of the 3H and 5H isomers depe