Cooperation between the Cu+ and Cu2+ species in CuCoAl layered double hydroxide and the substrate promoting effect afford a really simple protocol for the efficient synthesis of quinazolines
Author:
Affiliation:
1. Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Changzhou University, 213164 Changzhou, China
2. Jiangsu Lingfei Chemical Co., LTD, Wuxi 214264, China
3. Jiangsu Yabang Dyestuff Co., LTD, 213163 Changzhou, China
Abstract
Funder
Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology Department
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB00481G
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1. Design, Synthesis, and Biological Evaluation of Heterocyclic-Fused Pyrimidine Chemotypes Guided by X-ray Crystal Structure with Potential Antitumor and Anti-multidrug Resistance Efficacy Targeting the Colchicine Binding Site
2. Room temperature ligand-free Cu2O–H2O2 catalyzed tandem oxidative synthesis of quinazoline-4(3H)-one and quinazoline derivatives
3. Investigation of Janus Kinase (JAK) Inhibitors for Lung Delivery and the Importance of Aldehyde Oxidase Metabolism
4. Discovery of Quinazoline-2,4(1H,3H)-dione Derivatives Containing 3-Substituted Piperizines as Potent PARP-1/2 Inhibitors─Design, Synthesis, In Vivo Antitumor Activity, and X-ray Crystal Structure Analysis
5. Monodentate Transient Directing Group Assisted Ruthenium(II)-Catalyzed Direct ortho-C–H Imidation of Benzaldehydes for Diverse Synthesis of Quinazoline and Fused Isoindolinone
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