A Rapid Intramolecular Imino Diels-Alder Reaction of Aminoanthraquinones with Citronellal or Prenylated Salicylaldehydes: Substituent Effect on Changing the Reaction Pathway from Diels-Alder to Ene-Type Cyclization
Author:
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry,Catalysis
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2007-983790.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
1. The First Domino Reduction/Imine Formation/Intramolecular Aza-Diels-Alder Reaction for the Diastereoselective Preparation of Tetrahydrochromano[4,3-b]quinolines;European Journal of Organic Chemistry;2016-11-03
2. On-Demand Selection of the Reaction Path from Imino Diels-Alder to Ene-Type Cyclization: Synthesis of Epiminopyrimido[4,5-b]azepines;European Journal of Organic Chemistry;2013-11-19
3. A Facile Synthesis of Highly Substituted Five-Membered Rings: Mukaiyama-Aldol-Oxonoium-Ene (MAOE) Domino Reaction;Chemistry - An Asian Journal;2011-05-06
4. Asymmetric Synthesis of 4-Amino-4H-Chromenes by Organocatalytic Oxa-Michael/Aza-Baylis-Hillman Tandem Reactions;Chemistry - A European Journal;2010-07-26
5. Perchloric Acid and Its Salts: Very Powerful Catalysts in Organic Chemistry;Chemical Reviews;2010-03-17
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