93607-01-3Relevant academic research and scientific papers
An efficient alkynylation of 4-thiazolidinone with terminal alkyne under C-H functionalisation
Shaikh, Mohammed Umar M.,Mudaliar, Sulochana S.,Chikhalia, Kishor H.
, p. 50780 - 50785 (2016/06/09)
A method of palladium catalysed efficient alkynylation through the cross coupling reaction of terminal alkynes with the slightly more acidic C-H bonds of 4-thiazolidinone has been developed. This method allows the direct introduction of an ethynyl group into the 4-thiazolidinone moiety. Mild reaction conditions involving aerial oxidation and one pot synthesis make this reaction more efficient for the formation of sp3(C)-sp(C) bond.
An efficient and convenient protocol for the synthesis of thiazolidin-4-ones
Ebrahimi,Mobinikhaldei,Eibagi
experimental part, p. 2279 - 2285 (2012/03/26)
Without a catalyst and under solvent-free conditions, 2,3-disubstituted-1, 3- thiazolidin-4-one 5a-j derivatives were synthesized efficiently via the three-component reaction of aryl hydrazide, aromatic aldehyde, and mercaptoacetic acid. All the newly synthesized compounds were confirmed by IR, 1H NMR, and 13C NMR spectroscopy and elemental analysis. Copyright Taylor & Francis Group, LLC.
Synthesis and antimicrobial activity of 5-amino-2,7-diaryl-6-cyano-3- isonicotinamido thiazolo[4,5-b]-2,3,4,7-tetrahydropyridines, 2,7-diaryl-6-cyano-3-isonicotinamidothiazolo[4,5-b]-2,3,4,5,6, 7-hexahydropyrid-5-ones, 2,7-diaryl-5-amino-3-isonicotinamido
Khan, Mukhtar Hussain
, p. 148 - 153 (2008/02/09)
5-Amino-2,7-diaryl-6-cyano-3-isonicotinamido thiazolo[4,5-b]-2,3,4,7- tetrahydropyridines 3 and 2,7-diaryI-6-cyano-3-isonicotinamido thiazolo[4,5-b]-2,3,4,5,6,7-hexahydropyrid-5-ones 4 have been prepared by Michael addition between α,βunsaturated ketones
