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Palladium‐catalyzed cross‐coupling reactions of coumarin derivatives: An overview
Coumarins are omnipresent in several plants and exhibit a plethora of pharmacological properties, making them an important scaffold in organic synthesis. Naturally, the chemistry of this motif has attracted ever‐increasing attention, among which palladium‐catalyzed coupling reactions are the most pr...
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Published in: | Applied organometallic chemistry 2020-12, Vol.34 (12), p.n/a |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Coumarins are omnipresent in several plants and exhibit a plethora of pharmacological properties, making them an important scaffold in organic synthesis. Naturally, the chemistry of this motif has attracted ever‐increasing attention, among which palladium‐catalyzed coupling reactions are the most prevalent one. Numerous useful, easy, and concise syntheses and reactions have been achieved using palladium‐catalyzed coupling reactions. This review focuses on recent advances in palladium‐catalyzed cross‐coupling reactions such as Suzuki, Heck, Stille, Sonogoshira etc. reactions of coumarin derivatives and covers the literature from 2001 to 2020.
Coumarins generally have a broad range of biological activities which varies with its structure. Even though coumarins with different substituents at C‐3, C‐4 and C‐7 are explored using various reaction types, the positions C‐5, C‐6 and C‐8 remain relatively unexplored. Hence, there is a significant scope in this type of cross‐coupling reactions in coumarin chemistry for the development of functionalized and structurally diverse novel coumarin derivatives through placement of appropriate functional groups around the coumarin nucleus at different positions, which may be of potential biological interest. |
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ISSN: | 0268-2605 1099-0739 |
DOI: | 10.1002/aoc.5983 |