Synthesis of 2,3-disubstituted pyrazines and quinoxalines by Heck cross-coupling reactions of 2,3-dichloropyrazine and 2,3-dichloroquinoxaline. Influence of the temperature on the product distribution-Reference-Cited by-同舟云学术

Synthesis of 2,3-disubstituted pyrazines and quinoxalines by Heck cross-coupling reactions of 2,3-dichloropyrazine and 2,3-dichloroquinoxaline. Influence of the temperature on the product distribution

Published:2010-02 Issue:9 Volume:66 Page:1637-1642
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Malik Imran,Hussain Munawar,Ali Asad,Tengho Toguem Serge-Mithérand,Basha Fatima Z.,Fischer Christine,Langer Peter

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference38 articles.

1. Mechanisms responsible for the in vitro relaxation of ligustrazine on porcine left anterior descending coronary artery

2. Antimutagenicity of Maillard reaction products from amino acid/sugar model systems against 2-amino-3-methylimidazo-[4,5-f]quinoline: the role of pyrazines

3. Delayed Protection of Tetramethylpyrazine on Neonatal Rat Cardiomyocytes Subjected to Anoxia-Reoxygenation Injury

4. Novel alkaloids from the red ascidian botryllus leachi

5. Pharacine, a Natural p-Cyclophane and Other Indole Derivatives from Cytophaga sp. Strain AM13.1

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