| Autor: |
Zhu, Congjun, Yao, Shunruo, Xie, Jin |
| Předmět: |
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| Zdroj: |
Synthesis; Jun2024, Vol. 56 Issue 11, p1711-1718, 8p |
| Abstrakt: |
This article discusses the development of a visible-light-mediated three-component radical difunctionalization of alkenes, which allows for the synthesis of alkynyl-functionalized organoborons. The researchers optimized the reaction conditions and found that the use of specific reagents and a photocatalyst led to the desired product in good yield. The reaction was found to be chemoselective and had a broad substrate scope. The authors propose a plausible reaction mechanism based on their experimental findings. This method has potential applications in drug discovery and offers a feasible strategy for constructing alkynyl-functionalized organoborons. The text also provides detailed information about the physical and chemical properties of the product. Additionally, the document provides information on the synthesis and characterization of various chemical compounds, including derivatives of chroman and imidazole. The compounds are described in terms of their physical properties and spectroscopic data. Supporting information is available online. [Extracted from the article] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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