Development of a Dual Fries-Claisen Rearrangement Strategy
Author:
Affiliation:
1. School of Science & Technology, Nottingham Trent University
2. Research Institute for the Environment, Physical Sciences and Mathematics, Keele University
3. Chemistry Department, Loughborough University
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0031-1291158.pdf
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
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2. A new synthetic strategy to 2,3-diallyl-1,4-quinones via one-pot double Claisen rearrangement and retro Diels–Alder reaction;Tetrahedron Letters;2016-07
3. Synthesis of fused azacycle via Overman rearrangement and ring-rearrangement metathesis as key steps;Tetrahedron Letters;2016-05
4. Convenient synthesis of Bioactive Pyranonaphthoquinones (±)9-Demethoxyeleutherin and (±)9-Demethoxyisoeleutherin;Journal of Chemical Research;2014-09
5. Synthesis of Naturally Occurring Pyranonaphthoquinones: (±) 9-Demethoxyeleutherin, (±) 9-Demethoxyisoeleutherin, and Pentalongin via Nef Reaction;Synthetic Communications;2014-07-01
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