Organocatalytic (Z/E)-Selective Synthesis of 3-Vinylnaphthofurans via a Formal (3 + 2) Cycloaddition
Author:
Affiliation:
1. Research Center of Chiral Functional Heterocycles, School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou 221116, China
2. School of Petrochemical Engineering, Changzhou University, Changzhou 213164, China
Funder
Natural Science Foundation of Jiangsu Province
National Natural Science Foundation of China
Natural Science Foundation of the Jiangsu Higher Education Institutions
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c02641
Reference63 articles.
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2. Synthesis of Balsaminone A, a Naturally Occurring Pentacyclic Dinaphthofuran Quinone
3. A novel and efficient synthesis of diverse dihydronaphtho[1,2-b]furans using the ceric ammonium nitrate-catalyzed formal [3 + 2] cycloaddition of 1,4-naphthoquinones to olefins and its application to furomollugin
4. Genotoxicity of 2-nitro-7-methoxy-naphtho[2,1-b]furan (R7000): A case study with some considerations on nitrofurantoin and nifuroxazide
5. Synthesis of 1-(3′,4′,5′-trimethoxy) phenyl naphtho[2,1b]furan as a novel anticancer agent
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