Cu(I)-Catalyzed Asymmetric Multicomponent Cascade Inverse Electron-Demand Aza-Diels–Alder/Nucleophilic Addition/Ring-Opening Reaction Involving 2-Methoxyfurans as Efficient Dienophiles
Author:
Affiliation:
1. College of Chemistry and Molecular Sciences, Wuhan University, Hubei, China 430072
2. State Key Laboratory of Elemento-organic Chemistry, Nankai University, Tianjin, China 300071
Funder
State Administration of Foreign Experts Affairs
Ministry of Education of the People's Republic of China
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.6b01008
Reference35 articles.
1. Recent Developments in Catalytic Asymmetric Inverse-Electron-Demand Diels–Alder Reaction
2. Inverse electron demand Diels–Alder (iEDDA)-initiated conjugation: a (high) potential click chemistry scheme
3. Tandem inverse-electron-demand hetero-/retro-Diels–Alder reactions for aromatic nitrogen heterocycle synthesis
4. Asymmetric Three-Component Inverse Electron-Demand Aza-Diels-Alder Reaction: Efficient Synthesis of Ring-Fused Tetrahydroquinolines
5. Asymmetric Cycloaddition of β,γ-Unsaturated α-Ketoesters with Electron-Rich Alkenes Catalyzed by a Chiral Er(OTf)3/N,N′-Dioxide Complex: Highly Enantioselective Synthesis of 3,4-Dihydro-2 H-pyrans
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