CuCl2-catalyzed inexpensive, faster and ligand/additive free synthesis of isoquinolin-1(2H)-one derivatives via the coupling–cyclization strategy: Evaluation of a new class of compounds as potential PDE4 inhibitors-Reference-Cited by-同舟云学术

CuCl2-catalyzed inexpensive, faster and ligand/additive free synthesis of isoquinolin-1(2H)-one derivatives via the coupling–cyclization strategy: Evaluation of a new class of compounds as potential PDE4 inhibitors

Published:2021-10 Issue: Volume:115 Page:105265
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

Thirupataiah B.,Mounika Guntipally,Sujeevan Reddy Gangireddy,Sandeep Kumar Jetta,Kapavarapu Ravikumar,Medishetti Raghavender,Mudgal Jayesh,Mathew Jessy E.,Shenoy Gautham G.,Mallikarjuna Rao C.,Chatti Kiranam,V. L. Parsa Kishore,Pal Manojit

Funder

Manipal University

Department of Biotechnology, Ministry of Science and Technology, India

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

Reference40 articles.

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5. Non-Peptide Glycoprotein IIb/IIIa Antagonists. 11. Design and in Vivo Evaluation of 3, 4-Dihydro-1 (1 H)-isoquinolinone-Based Antagonists and Ethyl Ester Prodrugs;Hutchinson;J. Med. Chem.,1996

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