Synthetic approaches and pharmacological activity of 1, 3, 4-oxadiazoles: a review of the literature from 2000–2012
CS De Oliveira, BF Lira, JM Barbosa-Filho… - Molecules, 2012 - mdpi.com
Molecules | Free Full-Text | Synthetic Approaches and Pharmacological Activity of 1,3,4-Oxadiazoles:
A Review of the Literature from 2000–2012 Next Article in Journal Chemical Composition of …
A Review of the Literature from 2000–2012 Next Article in Journal Chemical Composition of …
Updates on synthesis and biological activities of 1, 3, 4-oxadiazole: A review
The new era of heterocyclic moieties which are developed in the decades plays a very
important role in the treatment of various diseases. Among them are 1, 3, 4-oxadiazoles, a …
important role in the treatment of various diseases. Among them are 1, 3, 4-oxadiazoles, a …
Cu (II) catalyzed imine C–H functionalization leading to synthesis of 2, 5-substituted 1, 3, 4-oxadiazoles
A direct access to symmetrical and unsymmetrical 2, 5-disubstituted [1, 3, 4]-oxadiazoles has
been accomplished through an imine C–H functionalization of N-arylidenearoylhydrazide …
been accomplished through an imine C–H functionalization of N-arylidenearoylhydrazide …
The reaction of (N-isocyanimino) triphenylphosphorane with benzoic acid derivatives: a novel synthesis of 2-aryl-1, 3, 4-oxadiazole derivatives
A Souldozi, A Ramazani - Tetrahedron Letters, 2007 - Elsevier
The reaction of (N-isocyanimino)triphenylphosphorane with benzoic acid derivatives: a
novel synthesis of 2-aryl-1,3,4-oxadiazole derivatives - ScienceDirect Skip to main contentSkip …
novel synthesis of 2-aryl-1,3,4-oxadiazole derivatives - ScienceDirect Skip to main contentSkip …
A facile procedure for the one-pot synthesis of unsymmetrical 2, 5-disubstituted 1, 3, 4-oxadiazoles
Unsymmetrically 2, 5-disubstituted 1, 3, 4-oxadiazoles were efficiently synthesized from the
cyclization–oxidation reaction of acyl hydrazones. Also, the synthesis of the title compounds …
cyclization–oxidation reaction of acyl hydrazones. Also, the synthesis of the title compounds …
Photoredox/Cobalt-Catalyzed Cascade Oxidative Synthesis of 2, 5-Disubstituted 1, 3, 4-Oxadiazoles under Oxidant-Free Conditions
JL Li, HY Li, SS Zhang, S Shen… - The Journal of Organic …, 2023 - ACS Publications
An efficient oxidant-free, photoredox-mediated cascade cyclization strategy for the synthesis
of 1, 3, 4-oxadiazoles by using an organo acridinium photocatalyst and a cobaloxime …
of 1, 3, 4-oxadiazoles by using an organo acridinium photocatalyst and a cobaloxime …
Greener and rapid access to bio-active heterocycles: one-pot solvent-free synthesis of 1, 3, 4-oxadiazoles and 1, 3, 4-thiadiazoles
V Polshettiwar, RS Varma - Tetrahedron Letters, 2008 - Elsevier
A novel one-pot solvent-free synthesis of 1, 3, 4-oxadiazoles and 1, 3, 4-thiadiazoles by
condensation of acid hydrazide and triethyl orthoalkanates under microwave irradiations is …
condensation of acid hydrazide and triethyl orthoalkanates under microwave irradiations is …
Microwave assisted syntheses of 2, 5-disubstituted 1, 3, 4-oxadiazoles
S Rostamizadeh, SAG Housaini - Tetrahedron letters, 2004 - Elsevier
Microwave assisted syntheses of 2,5-disubstituted 1,3,4-oxadiazoles - ScienceDirect Skip to
main contentSkip to article Elsevier logo Journals & Books Search RegisterSign in View PDF …
main contentSkip to article Elsevier logo Journals & Books Search RegisterSign in View PDF …
One pot direct synthesis of oxazolines, benzoxazoles, and oxadiazoles from carboxylic acids using the Deoxo-Fluor reagent
CO Kangani, DE Kelley, BW Day - Tetrahedron letters, 2006 - Elsevier
One pot direct synthesis of oxazolines, benzoxazoles, and oxadiazoles from carboxylic acids using
the Deoxo-Fluor reagent - ScienceDirect Skip to main contentSkip to article Elsevier logo Journals …
the Deoxo-Fluor reagent - ScienceDirect Skip to main contentSkip to article Elsevier logo Journals …
The reaction of (N‐isocyanimino) triphenylphosphorane with an electron‐poor α‐haloketone in the presence of aromatic carboxylic acids: A novel three‐component …
Reactions of electron‐poor α‐haloketones with (N‐isocyanimino) triphenylphosphorane in
the presence of aromatic carboxylic acids proceed smoothly at room temperature and in …
the presence of aromatic carboxylic acids proceed smoothly at room temperature and in …