Control of electron demand in the cycloadditions of 2(H)-1,4-oxazin-2-ones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. 2( H )-1,4-Oxazin-2-ones as ambident azadienes
2. 4,6-Dichloro-2-oxa-5-azabicyclo[2.2.2]oct-5-en-3-ones and their Use in the Synthesis of 1,6-Dihydro-6-oxo-2-pyridine- and 6-Oxo-2-piperidinecarboxylates
3. The Synthesis of 3-Functionalized 5-chloro-6-methyl-2H-1,4-oxazin-2-ones and of pyridines from cycloaddition-elimination reactions with substituted acetylenic compounds.
4. Ring transformations of 3-(diethylamino)-5-chloro-2(1H)-pyrazinones and the corresponding 2H-1,4-oxazin-2-ones on reaction with acetylenic compounds
Cited by 4 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. Indium triflate-catalysed Diels–Alder reactions of isochromenylium cations with enones;Organic & Biomolecular Chemistry;2013
2. 1,2,4-Triazine vs. 1,3- and 1,4-Oxazinones in Normal- and Inverse-Electron-Demand Hetero-Diels-Alder Reactions: Establishing a Status Quo by Computational Analysis;European Journal of Organic Chemistry;2010-12-22
3. Synthesis of Hydrophobically Modified Analogues of Adenophorine;Synlett;2007-06
4. Investigation of the Diels−Alder Cycloadditions of 2(H)-1,4-Oxazin-2-ones;The Journal of Organic Chemistry;2005-10-20
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