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CC BY-NC-ND 4.0 · SynOpen 2021; 05(03): 255-277
DOI: 10.1055/a-1589-9556
DOI: 10.1055/a-1589-9556
review
Synthesis and Reactivity of Electron-Deficient 3-Vinylchromones
The Russian Science Foundation (project No. 18-13-00186) is acknowledged for funding.
Dedicated to Dr. V. Yu. Korotaev on the occasion of his 50th birthday
Abstract
The reported methods and data for the synthesis and reactivity of electron-deficient 3-vinylchromones containing electron-withdrawing groups at the exo-cyclic double bond are summarized and systematized for the first time. The main methods for obtaining these compounds are Knoevenagel condensation, Wittig reaction, and palladium-catalyzed cross-couplings. The most important chemical properties are transformations under the action of mono- and dinucleophiles, ambiphilic cyclizations, and cycloaddition reactions. The cross-conjugated and polyelectrophilic dienone system in 3-vinylchromones provides their high reactivity and makes these compounds valuable building blocks for the preparation of more complex heterocyclic systems. Chemical transformations of 3-vinylchromones usually begin with an attack of the C-2 atom and are accompanied by the opening of the pyrone ring followed by recyclization, in which the carbonyl group of chromone, an exo-double bond or a substituent on it can take part. The mechanisms of the reactions are discussed, the conditions for their implementation are described, and the yields of the resulting products are given. This review focuses on an analysis and generalization of the knowledge that has accumulated on the chemistry of electron-deficient 3-vinylchromones, mostly over the past 15 years.
1 Introduction
2 Synthesis of 3-Vinylchromones
3 Reactions with Mononucleophiles
4 Reactions with Dinucleophiles
5 Ambiphilic Cyclization
6 Cycloaddition Reactions
7 Other Reactions
8 Conclusion
Key words
3-vinylchromones - nucleophilic reactions - ambiphilic cyclizations - cycloaddition reactions - heterocyclesPublication History
Received: 21 July 2021
Accepted after revision: 16 August 2021
Accepted Manuscript online:
17 August 2021
Article published online:
07 September 2021
© 2021. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
Georg Thieme Verlag KG
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