Doubly Decarboxylative Synthesis of 4-(Pyridylmethyl)chroman-2-ones and 2-(Pyridylmethyl)chroman-4-ones under Mild Reaction Conditions
The doubly decarboxylative Michael–type addition of pyridylacetic acid to chromone-3-carboxylic acids or coumarin-3-carboxylic acids has been developed. This protocol has been realized under Brønsted base catalysis, providing biologically interesting 4-(pyridylmethyl)chroman-2-ones and 2-(pyridylmet...
Main Authors: | Jan Bojanowski, Anna Albrecht |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-08-01
|
Series: | Molecules |
Subjects: | |
Online Access: | https://www.mdpi.com/1420-3049/26/15/4689 |
Similar Items
-
Enantioselective, Decarboxylative (3+2)-Cycloaddition of Azomethine Ylides and Chromone-3-Carboxylic Acids
by: Ewelina Kowalska, et al.
Published: (2022-10-01) -
Pd-catalyzed decarboxylative Heck vinylation of 2-nitrobenzoates in the presence of CuF2
by: Lukas J. Gooßen, et al.
Published: (2010-05-01) -
Hypervalent iodine(III)-mediated decarboxylative acetoxylation at tertiary and benzylic carbon centers
by: Kensuke Kiyokawa, et al.
Published: (2018-05-01) -
Influence of Solvent, Electron Acceptors and Arenes on Photochemical Decarboxylation of Free Carboxylic Acids via Single Electron Transfer (SET)
by: Yasuharu Yoshimi, et al.
Published: (2010-04-01) -
Radical Decarboxylative Carbon–Nitrogen Bond Formation
by: Xiangting Li, et al.
Published: (2023-05-01)