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- W2316808757 endingPage "19595" @default.
- W2316808757 startingPage "19592" @default.
- W2316808757 abstract "Taking advantage of Rh(III)-catalyzed C–H activation reactions, we have developed a mild, short, and efficient method for the synthesis of bench-stable 3-isoquinolone MIDA boronates. The reaction is practical and scalable. The product formed has been applied in the Suzuki–Miyaura reaction with high efficiency. This strategy has also been successfully expanded to the synthesis of MIDA boronate functionalized heterocycles such as isoquinoline, pyrrole, and indole." @default.
- W2316808757 created "2016-06-24" @default.
- W2316808757 creator A5017167322 @default.
- W2316808757 creator A5049248960 @default.
- W2316808757 creator A5061873555 @default.
- W2316808757 creator A5081906849 @default.
- W2316808757 date "2012-11-20" @default.
- W2316808757 modified "2023-09-28" @default.
- W2316808757 title "Mild Rh(III)-Catalyzed C–H Activation and Annulation with Alkyne MIDA Boronates: Short, Efficient Synthesis of Heterocyclic Boronic Acid Derivatives" @default.
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- W2316808757 doi "https://doi.org/10.1021/ja310153v" @default.
- W2316808757 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23146122" @default.
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