Regioselective Dearomatization of N ‐Alkylquinolinium and Pyridinium Salts under Morita‐Baylis‐Hillman Conditions
Author:
Affiliation:
1. Centre of New Technologies University of Warsaw Banacha 2C 02-097 Warsaw Poland
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202200429
Reference80 articles.
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2. Recent Advances in the Baylis−Hillman Reaction and Applications
3. The Enantioselective Morita–Baylis–Hillman Reaction and Its Aza Counterpart
4. Enantioselektive Morita-Baylis-Hillman-Reaktionen und ihre Aza-Varianten
5. aza-Baylis−Hillman Reaction
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2. Facile Construction of Benzo[d][1,3]oxazocine: Reductive Radical Dearomatization of N-Alkyl Quinoline Quaternary Ammonium Salts;Organic Letters;2024-03-04
3. Direct Dearomatization of Quinoline/Isoquinoline Ammonium Halides to Construct N‐Substituted Tetrahydroquinolines and Tetrahydroisoquinolines;ChemistrySelect;2024-01-18
4. Chemoselective Intramolecular Morita–Baylis–Hillman Reaction; Acrylamide and Ketone as Sluggish Reacting Partners on a Labile Framework;The Journal of Organic Chemistry;2024-01-02
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