Aminoalkylation of Electron-Rich Aromatic Compounds Using Performed Iminium Salts Derived from Aldehydes other than Formaldehyde-Reference-Cited by-同舟云学术

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Aminoalkylation of Electron-Rich Aromatic Compounds Using Performed Iminium Salts Derived from Aldehydes other than Formaldehyde

Published:1996-07 Issue:07 Volume:1996 Page:883-887
ISSN:0039-7881
Container-title:Synthesis
language:
Short-container-title:Synthesis

Author:

Grumbach Hans-Joachim,Arend Michael,Risch Nikolaus

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Catalysis

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-1996-4301.pdf

Cited by 40 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. Multicomponent double Mannich alkylamination involving C(sp2)–H and benzylic C(sp3)–H bonds;Nature Communications;2022-01-21

2. Terminal Acetylenic Iminium Salts – Synthesis and Reactivity;European Journal of Organic Chemistry;2018-12-27

3. Magnetic nanocrystallites strontium hexaferrite as an efficient catalyst in the green Betti reaction;Inorganic and Nano-Metal Chemistry;2018-10-03

4. 2-Naphthol-pyrazole conjugates as substrates in the Mannich reaction;Zeitschrift für Naturforschung B;2018-03-20

5. Three-component, solvent-free synthesis of Betti base catalyzed by sulfated polyborate;Monatshefte für Chemie - Chemical Monthly;2018-02-14

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