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Site-selective C–H activation and regiospecific annulation using propargylic carbonates† †Electronic supplementary information (ESI) available. CCDC 1866187. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c9sc01703h

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Herein we describe an unprecedented RuII-catalyzed site-selective and regiospecific annulation of benzoic acids with propargylic carbonates. The weakly coordinating carboxylic acid moiety outperformed other typically used directing groups in C–H… Click to show full abstract

Herein we describe an unprecedented RuII-catalyzed site-selective and regiospecific annulation of benzoic acids with propargylic carbonates. The weakly coordinating carboxylic acid moiety outperformed other typically used directing groups in C–H activation, including ketone, nitrile, sulfonamide, amide and strongly coordinating nitrogen heterocycles.

Keywords: site selective; regiospecific annulation; esi; propargylic carbonates

Journal Title: Chemical Science
Year Published: 2019

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