Literature DB >> 29779224

Iridium-Catalyzed, Silyl-Directed, peri-Borylation of C-H Bonds in Fused Polycyclic Arenes and Heteroarenes.

Bo Su1, John F Hartwig1.   

Abstract

peri-Disubstituted naphthalenes exhibit interesting phyn class="Chemical">sical properties and unique chemical reactivity, due to the parallel arrangement of the bonds to the two peri-disposed substituents. Regioselective installation of a functional group at the position peri to 1-substituted naphthalenes is challenging due to the steric interaction between the existing substituent and the position at which the second one would be installed. We report an iridium-catalyzed borylation of the C-H bond peri to a silyl group in naphthalenes and analogous polyaromatic hydrocarbons. The reaction occurs under mild conditions with wide functional group tolerance. The silyl group and the boryl group in the resulting products are precursors to a range of functional groups bound to the naphthalene ring through C-C, C-O, C-N, C-Br and C-Cl bonds.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  C−H activation; borylation; catalysis; naphthalene; polyaromatic hydrocarbons

Year:  2018        PMID: 29779224      PMCID: PMC7484944          DOI: 10.1002/anie.201805086

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  55 in total

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7.  Lewis Acid-Base Interaction-Controlled ortho-Selective C-H Borylation of Aryl Sulfides.

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9.  Palladium-catalyzed C8 alkylation of 1-naphthylamides with alkyl halides via bidentate-chelation assistance.

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1.  Overcoming peri- and ortho-selectivity in C-H methylation of 1-naphthaldehydes by a tunable transient ligand strategy.

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