One-Step Synthesis of Naphthofurandione, Benzofurandione, and Phenalenofuranone Derivatives by the CAN-Mediated Cycloaddition
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/71/7/71_7_1691/_pdf
Reference45 articles.
1. Furanonaphthoquinones from Tabebuia ochracea ssp. neochrysanta
2. Photoinduced molecular transformations. 140. New one-step general synthesis of naphtho[2,3-b]furan-4,9-diones and their 2,3-dihydro derivatives by the regioselective [3 + 2] photoaddition of 2-hydroxy-1,4-naphthoquinones with various alkynes and alkenes: application of the photoaddition to a two-step synthesis of maturinone
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1. Naphtho[2,3-b]furan-4,9-dione synthesis via palladium-catalyzed reverse hydrogenolysis;Chemical Communications;2019
2. Advanced Routes in Synthesis and Reactions of Lawsone Molecules (2-Hydroxynaphthalene-1,4-dione);Journal of Heterocyclic Chemistry;2017-05-03
3. Lawsone in organic synthesis;RSC Advances;2015
4. A facile, three-component domino protocol for the microwave-assisted synthesis of functionalized naphtho[2,3-b]furan-4,9-diones in water;Green Chemistry;2011
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