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- W2890943724 endingPage "14895" @default.
- W2890943724 startingPage "14891" @default.
- W2890943724 abstract "Abstract A BF 3 ⋅Et 2 O‐catalyzed C2‐selective C−H borylation of indoles with bis(pinacolato)diboron was developed to afford indole‐2‐boronic acid pinacol esters. A variety of functional groups were tolerated, and other heteroarenes like pyrrole and benzo[ b ]thiophene were also suitable substrates. An electrophilic substitution mechanism was proposed based on the preliminary mechanistic studies. This novel transformation utilizes simple and cheap BF 3 ⋅Et 2 O as catalyst and exhibits unusual C2 regioselectivity, providing a significant non‐transition‐metal‐catalyzed C−H borylation and an efficient method towards the synthesis of C2‐functionalized heteroarenes." @default.
- W2890943724 created "2018-09-27" @default.
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- W2890943724 creator A5058846208 @default.
- W2890943724 creator A5079341905 @default.
- W2890943724 creator A5090818891 @default.
- W2890943724 date "2018-10-12" @default.
- W2890943724 modified "2023-10-11" @default.
- W2890943724 title "Boron(III)‐Catalyzed C2‐Selective C−H Borylation of Heteroarenes" @default.
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- W2890943724 doi "https://doi.org/10.1002/anie.201808590" @default.
- W2890943724 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30203906" @default.
- W2890943724 hasPublicationYear "2018" @default.
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