Abstract
Radical cascade cyclization reactions are widely employed in the synthesis of functionalized heterocycles due to their numerous advantages. This review carefully compiles and analyzes recent advancements in the construction of 2-functionalized thioflavones through radical cascade cyclization reactions, emphasizing their potential and versatility in generating a range of valuable thioflavone products. These strategies enable the efficient synthesis of diverse 2-functionalized thioflavones via heat- or light-promoted reactions using methylthiolated alkynones as the acceptor substrate. In this review, we aim to provide a thorough overview of the state-of-the-art approaches by exploring the mechanisms and scope of these reactions, while serving as a vital reference for future research and industrial applications in thioflavones synthesis.
Original language | English |
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Journal | Asian Journal of Organic Chemistry |
DOIs | |
Publication status | Accepted/In press - 2025 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2025 Wiley-VCH GmbH.
ASJC Scopus Subject Areas
- Organic Chemistry
Keywords
- 2-Functionalized thioflavones
- Methylthiolated alkynones
- Organic synthesis
- Radical cascade cyclization
- Radical chemistry