Exploration of polystyrene-supported 2-isobutoxy-1-isobutoxycarbonyl-1,2-dihydroquinoline (PS-IIDQ) as new coupling agent for the synthesis of 8-substituted xanthine derivatives-Reference-Cited by-同舟云学术

Exploration of polystyrene-supported 2-isobutoxy-1-isobutoxycarbonyl-1,2-dihydroquinoline (PS-IIDQ) as new coupling agent for the synthesis of 8-substituted xanthine derivatives

Published:2012-08 Issue:35 Volume:53 Page:4631-4635
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Bandyopadhyay Prabal,Sathe Manisha,Sharma Pratibha,Kaushik M.P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference21 articles.

1. Adenosine Receptor Antagonists: Translating Medicinal Chemistry and Pharmacology into Clinical Utility

2. Recent developments in adenosine receptor ligands and their potential as novel drugs

3. Adenosine receptors: pharmacology, structure-activity relationships, and therapeutic potential

4. A facile and rapid one-step synthesis of 8-substituted xanthine derivatives via tandem ring closure at room temperature

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Recent Developments towards the Synthesis of Pyrimidopyrimidine and Purine Derivatives;ChemistrySelect;2023-07-10

2. Solvent-Free Mechanosynthesis of Polysubstituted 1,2-Dihydroquinolines from Anilines and Alkyne Esters;The Journal of Organic Chemistry;2022-06-22

3. Synthesis of Pyrimidine-Annulated Five-Membered Heterocycles: An Overview;Current Organic Chemistry;2019-12-24

4. A One-Pot Synthesis of 5-(1,3-Dimethyl-2,6-Dioxo-5-{[(1E)-Arylmethylene]Amino}-1,2,3,6-Tetrahydropyrimidin-4-yl)-1,3,7,9-Tetramethyl-5,10-Dihydropyrimido[5,4-g]Pteridine-2,4,6,8(1H,3H,7H,9H)-Tetrone via a Pseudo Four-Component Domino Reaction;Polycyclic Aromatic Compounds;2019-10-18

5. Pd-Catalyzed Decarboxylative Cyclization of Trifluoromethyl Vinyl Benzoxazinanones with Sulfur Ylides: Access to Trifluoromethyl Dihydroquinolines;Organic Letters;2019-02-21