An Efficient Green Protocol for Synthesis of 2,3‐Dihydroquinazolin‐4(1H)‐ones Using SBA‐16/GPTMS‐TSC‐CuIunder Solvent‐Free Conditions
Author:
Affiliation:
1. Department of Chemistry, Faculty of ScienceFerdowsi University of Mashhad Mashhad 9177948974 Iran
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.201904356
Reference93 articles.
1. A. R. Katritzky C. W. Rees E. F. V. Scriven Comprehensive Heterocyclic Chemistry II (Pergamon Oxford 1996)
2. J. A. Joule K. Mills Heterocyclic Chemistry (Blackwell Science Oxford. 2000)
3. Highly efficient solvent-free synthesis of quinazolin-4(3H)-ones and 2,3-dihydroquinazolin-4(1H)-ones using tetrabutylammonium bromide as novel ionic liquid catalyst
4. Synthesis, characterization, and application of Fe3O4-SA-PPCA as a novel nanomagnetic reusable catalyst for the efficient synthesis of 2,3-dihydroquinazolin-4(1H)-ones and polyhydroquinolines
5. Synthesis of 2,3-dihydroquinazolin-4(1H)-ones via one-pot three-component reaction catalyzed by l-pyrrolidine-2-carboxylic acid-4-hydrogen sulfate (supported on silica gel) as novel and recoverable catalyst
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1. An eco‐friendly, sustainable, and greener approach to the synthesis of Dihydroquinazolin‐4(1H)‐ones using a deep eutectic solvent;Journal of Heterocyclic Chemistry;2023-12-10
2. Alginic acid in water at room temperature: a natural combination for the environmental benign synthesis of 2,3-dihydroquinazolin-4(1H)-ones;Research on Chemical Intermediates;2023-10-16
3. Preparation of a novel acidic functionalized diatomite and its catalytic application in the synthesis of 2,3-dihydroquinazolin-4(1H)-one derivatives;Research on Chemical Intermediates;2022-12-21
4. Preparation and application of ZnFe2O4@SiO2–SO3H, as a novel heterogeneous acidic magnetic nanocatalyst for the synthesis of tetrahydrobenzo[b]pyran and 2,3-dihydroquinazolin-4(1H)-one derivative;Research on Chemical Intermediates;2022-12-07
5. Synthesis of a Pyrrolo[1,2-a]quinazoline-1,5-dione Derivative by Mechanochemical Double Cyclocondensation Cascade;Molecules;2022-09-02
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