Iodine-induced Oxidative Cyclisation ofN-Acyl Amidines: A Rapid Synthesis of 3,5-Disubstituted-1,2,4-Oxadiazoles
Author:
Affiliation:
1. Medicinal and Process Chemistry Division; CSIR-Central Drug Research Institute B.S.10/1, Sector-10, Jankipuram Extension; Lucknow 226 031 India
Publisher
Wiley
Subject
General Chemistry
Reference48 articles.
1. Green Solvents in Carbohydrate Chemistry: From Raw Materials to Fine Chemicals
2. Catalytic Chalcogenylation under Greener Conditions: A Solvent-Free Sulfur- and Seleno-functionalization of Olefins via I2/DMSO Oxidant System
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1. Direct synthesis of 3,5‐diaryl‐1,2, 4‐oxadiazoles using 1‐(2‐oxo‐2‐arylethyl)pyridin‐1‐iums with benzamidines;Journal of Heterocyclic Chemistry;2021-08-28
2. One-pot synthesis of 3,5-diaryl substituted-1,2,4-oxadiazoles using gem-dibromomethylarenes;Canadian Journal of Chemistry;2019-09
3. Efficient Copper-Catalyzed Multicomponent Synthesis of N-Acyl Amidines via Acyl Nitrenes;Journal of the American Chemical Society;2019-08-29
4. Synthesis, Antitumor and Cytotoxic Activity of New Adamantyl O ‐Acylamidoximes and 3‐Aryl‐5‐Adamantane‐1,2,4‐Oxadiazole Derivatives;ChemistrySelect;2019-08-19
5. NBS-mediated practical cyclization of N-acyl amidines to 1,2,4-oxadiazoles via oxidative N‒O bond formation;Tetrahedron;2018-08
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