1181219-12-4Relevant articles and documents
Synthesis, characterization and antimicrobial evaluation of 2-phenylpropanoic acid derived new oxadiazoles
Fuloria, Neeraj K.,Fuloria, Shivkanya,Balaji, Kaveti,Karupiah, Sundram,Sathasivam, Kathiresan,Jain, Ajay,Sridevi, Ugrappa,Himaja, Malipeddi
, p. 37 - 42 (2019/01/18)
2-Phenylpropanoic acid and oxadiazoles are known to possess antimicrobial potential. 2- phenylpropanehydrazide (2), a derivative of methyl 2-phenylpropionate, on cyclization with aromatic acids offered new 2-aryl-5-(1-phenylethyl)-1,3,4-oxadiazole derivat
Copper-catalyzed direct cross-coupling of 1,3,4-oxadiazoles with N-tosylhydrazones: Efficient synthesis of benzylated 1,3,4-oxadiazoles
Salvanna,Reddy, Gandolla Chinna,Rao, Bethapudi Rama,Das, Biswanath
, p. 20538 - 20544 (2013/11/06)
The first copper catalyzed direct C-H benzylation of 1,3,4-oxadiazoles using N-tosylhydrazones has efficiently been accomplished. Several substituted oxadiazoles have been prepared in high yields (80-89%) in 3 h. The Royal Society of Chemistry 2013.
Nickel-catalyzed C-H alkenylation and alkylation of 1,3,4-oxadiazoles with alkynes and styrenes
Mukai, Tomoya,Hirano, Koji,Satoh, Tetsuya,Miura, Masahiro
experimental part, p. 6410 - 6413 (2009/12/06)
(Chemical Equation Presented) The addition reaction of 1,3,4-oxadiazoles to alkynes via C-H bond cleavage efficiently proceeds in the presence of a nickel catalyst. This direct coupling allows a facile access to alkenyl-substituted oxadiazoles. The reaction with styrenes in place of alkynes is also available to selectively afford the corresponding branched adducts.
