New Efficient Route to Dissymmetric 2,4-Di(het)aryl-pyrido[3,2-d]pyrimidines via Regioselective Cross-Coupling Reactions-Reference-Cited by-同舟云学术

New Efficient Route to Dissymmetric 2,4-Di(het)aryl-pyrido[3,2-d]pyrimidines via Regioselective Cross-Coupling Reactions

Published:2007-10-20 Issue:23 Volume:9 Page:4673-4676
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Tikad Abdellatif¹,Routier Sylvain¹,Akssira Mohamed¹,Leger Jean-Michel¹,Jarry Christian¹,Guillaumet Gérald¹

Affiliation:

1. ICOA UMR 6005 CNRS, Université d'Orléans, F-45067, Orléans, France, LCBA Université Hassan II-Mohammedia, BP 146, 20650 Mohammedia, Morocco, and EA 2962, Pharmacochimie, Universite Victor Segalen Bordeaux II, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol7014434

Reference19 articles.

1. Regioselective cross-coupling reactions of multiple halogenated nitrogen-, oxygen-, and sulfur-containing heterocycles

2. Small Molecule Inhibitors of Tumor-Promoted Angiogenesis, Including Protein Tyrosine Kinase Inhibitors

3. p38MAP kinase inhibitors. part 1: design and development of a new class of potent and highly selective inhibitors based on 3,4-dihydropyrido[3,2-d]pyrimidone scaffold

4. Synthesis and biological evaluation of 6,7-disubstituted 4-aminopyrido[2,3-d]pyrimidines as adenosine kinase inhibitors

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