5-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridine is a key component in chemical synthesis, particularly in the field of organic chemistry. This compound serves as a versatile building block for the construction of complex molecules due to its unique structural features. In synthesis, 5-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridine can be employed as a valuable reagent for the formation of carbon-carbon and carbon-heteroatom bonds. Its fluoro-substituted moiety enhances its reactivity and selectivity in various coupling reactions, such as Suzuki-Miyaura cross-coupling, Sonogashira coupling, and Heck reactions.Furthermore, the boron-containing functionality in this compound offers additional synthetic opportunities, as it can participate in diverse transformations including boronate ester formation, borylation reactions, and subsequent functional group manipulations. This enables the precise control of regioselectivity and the introduction of boron motifs into target molecules for further derivatization.Overall, the strategic incorporation of 5-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridine in chemical synthesis facilitates the efficient assembly of structurally complex and biologically relevant compounds with high synthetic efficiency and control.
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(Cl)Cl)c1c(C)cc(cc1C)C](https://img.angenechemical.com/storage/6693/66939a3f08a27d2b6717c3194e00970b.png)
