Ready and selective access to 2-arylquinazolines from α-amino acids via a new solvent-free domino transformation under synergistic nano Fe-Mo-Se catalyst-Reference-Cited by-同舟云学术

Ready and selective access to 2-arylquinazolines from α-amino acids via a new solvent-free domino transformation under synergistic nano Fe-Mo-Se catalyst

Published:2020-12 Issue: Volume:92 Page:96-100
ISSN:1226-086X
Container-title:Journal of Industrial and Engineering Chemistry
language:en
Short-container-title:Journal of Industrial and Engineering Chemistry

Author:

Nguyen Khang X.,Pham Phuc H.,Nguyen An C.D.,Nguyen Chuc T.,Nguyen Tung T.,Tran Phong D.,Phan Nam T.S.

Publisher

Elsevier BV

Subject

General Chemical Engineering

Reference29 articles.

1. One-Pot Synthesis of 2-Arylquinazolines and Tetracyclic Isoindolo[1,2-a]quinazolinesviaCyanation Followed by Rearrangement ofortho-Substituted 2-Halo-N-arylbenzamides

2. Synthesis of 2-substituted quinazolines by CsOH-mediated direct aerobic oxidative cyclocondensation of 2-aminoarylmethanols with nitriles in air

3. Efficient aerobic oxidative synthesis of 2-aryl quinazolines via benzyl C–H bond amination catalyzed by 4-hydroxy-TEMPO

4. Accessing Polysubstituted Quinazolines via Nickel Catalyzed Acceptorless Dehydrogenative Coupling

5. An insight into the therapeutic potential of quinazoline derivatives as anticancer agents

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