Mn(OAc) 3 *2H 2 O promoted addition of arylboronic acids to quinoxalin-2-ones
Author:
Funder
UGC
CSIR
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference66 articles.
1. Design and Synthesis of Potent and Multifunctional Aldose Reductase Inhibitors Based on Quinoxalinones
2. Design, Synthesis, and Biological Activity of Potent and Selective Inhibitors of Blood Coagulation Factor Xa
3. Potent Platelet-Derived Growth Factor-.BETA. Receptor (PDGF-.BETA.R) Inhibitors: Synthesis and Structure-Activity Relationships of 7-[3-(Cyclohexylmethyl)ureido]-3-{1-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl}quinoxalin-2(1H)-one Derivatives
4. Convenient Synthetic Method for 3-(3-Substituted indol-2-yl)quinoxalin-2-ones as VEGF Inhibitor
5. Prolyl Oligopeptidase Inhibition by N-Acyl-pro-pyrrolidine-type Molecules
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