Synthesis of 2-aryl quinazolinones via iron-catalyzed cross-dehydrogenative coupling (CDC) between N–H and C–H bonds
Author:
Affiliation:
1. Research Institute of Pharmaceutical Sciences
2. College of Pharmacy
3. Seoul National University
4. Seoul
5. Republic of Korea
Abstract
Iron-catalyzed cross-dehydrogenative coupling between methyl arenes and anthranilamides for the direct synthesis of quinazolinones.
Funder
National Research Foundation of Korea
Seoul National University
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB00866D
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3. Targeting the α-folate receptor with cyclopenta[g]quinazoline-based inhibitors of thymidylate synthase
4. Synthesis and antihypertensive activity of novel 3-benzyl-2-substituted-3H-[1,2,4]triazolo[5,1-b]quinazolin-9-ones
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