Chemical Research Letters, May 2021. The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry. 766-36-9, Name is 3-Ethyl-4-methyl-2,5-dihydro-1H-pyrrol-2-one, SMILES is O=C1NCC(C)=C1CC, in an article , author is Saudi, MNS, once mentioned of 766-36-9, Quality Control of 3-Ethyl-4-methyl-2,5-dihydro-1H-pyrrol-2-one.
Synthesis of some 3-and 4-substituted 1,5-diphenylpyrrolidine-2,4-diones as potential antimicrobial and antineoplastic agents – Reactions with tetramic acid, part 5
The condensation of 1,5-diphenylpyrrolidine-2,4-dione (1) with the carboxyl compounds 2a-f afforded the corresponding 3-arylidene-1,5-diphenylpyrrolidine-2,4-diones 3a-f. Reaction of the parent compound 1 with isatin (4) yielded the condensation product 5 in an acidic medium, whereas compound 6 was obtained in an alkaline medium. The condensation of the primary amines 7a-f with compound 1 afforded the corresponding 4-substituted amino- 1,5 -diphenyl-Delta(3) -pyrrolin-2-ones 8a-f. All the compounds synthesized were screened for their antimicrobial activity, and four compounds were selected for screening for their antineoplastic activity. The compounds tested showed both antimicrobial and antineoplastic activities.
The prevalence of solvent effects in heterogeneous catalysis in condensed media has motivated developing quantitative kinetic, their interactions with reaction intermediates. Interested yet? Read on for other articles about 766-36-9. Quality Control of 3-Ethyl-4-methyl-2,5-dihydro-1H-pyrrol-2-one.
Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem