Cycloaddition Reactions of Azepines and Diazepines with Conjugated Double Bonds Possessing Electron-Withdrawing Groups
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/57/12/57_12_3483/_pdf
Reference22 articles.
1. Unsaturated heterocyclic systems. XLVI. Molecular geometry of derivatives of 1H-azepine in the free and complexed state
2. 1,4-cycloaddition of nitrosobenzene to N-ethoxycarbonylazepine
3. 1,4-cycloaddition of nitrosobenzene to N-ethoxycarbonylazepine
4. Frontier-controlled pericyclic reactions of powerful electron-attracting cyclic dienones and diazadienones with 1H-azepine: molecular structures of cycloadducts and some comments
5. Cycloaddition of Azepine Derivatives with Methoxycarbonyl-2-pyrones
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1. Inverse-electron-demand Diels–Alder reactions of α,β-unsaturated hydrazones with 3-methoxycarbonyl α-pyrones;Organic & Biomolecular Chemistry;2018
2. Seven-Membered Heterocycles: Azepines, Benzo Derivatives and Related Systems;Modern Heterocyclic Chemistry;2011-07-27
3. Alder-Rickert Reaction;Comprehensive Organic Name Reactions and Reagents;2010-09-15
4. Diels−Alder Reactions of Fused Pyran-2-ones with Maleimides: Efficient Syntheses of Benz[e]isoindoles and Related Systems;Organic Letters;2003-07-08
5. [6 + 4] Cycloaddition Reactions;Organic Reactions;1996-10-18
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