Regioselective Copper(I)-Catalyzed Ullmann Amination of Halopyridyl Carboxylates using Sodium Azide: A Route for Aminopyridyl Carboxylates and their Transformation to Pyrido[2, 3-d]pyrimidin-4(1H)-ones-Reference-Cited by-同舟云学术

Regioselective Copper(I)-Catalyzed Ullmann Amination of Halopyridyl Carboxylates using Sodium Azide: A Route for Aminopyridyl Carboxylates and their Transformation to Pyrido[2, 3-d]pyrimidin-4(1H)-ones

Published:2018-05-03 Issue:17 Volume:3 Page:4822-4826
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
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Author:

Nisha ¹^ORCID,Sharma Mr. Chetan²,Kumar Rupesh²,Kumar Yogesh²³^ORCID

Affiliation:

1. Department of Chemistry; Faculty of Physical Sciences; SGT University; Gurugram Haryana-122505 India

2. Department of Chemical Sciences; IKG Punjab Technical University; Kapurthala Punjab-144603 India

3. UNAM-National Nanotechnology Research Center; Institute of Materials Science and Nanotechnology and Department of Chemistry; Bilkent University; 06800 Ankara Turkey

Funder

Umeå University

Publisher

Wiley

Subject

General Chemistry

Reference72 articles.

1. Amino Group Chemistry: From Synthesis to the Life Sciences 2008

2. Recent Advances in Metal-Mediated Carbon-Nitrogen Bond Formation Reactions: Aziridination and Amidation

3. Towards mild metal-catalyzed C–H bond activation

4. Cross-Dehydrogenative Coupling (CDC): Exploring C−C Bond Formations beyond Functional Group Transformations

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