ChemInform Abstract: Iridium-Catalyzed Borylation of Primary Benzylic C-H Bonds Without a Directing Group: Scope, Mechanism, and Origins of Selectivity
The borylation of methylarenes with a silylborane reagent and a new iridium catalyst containing an electron‐deficient phenanthroline ligand selectively leads to benzylic boronate esters over the corresponding aryl boronate esters.
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Veröffentlicht in: | ChemInform 2015-12, Vol.46 (51), p.no-no |
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creator | Larsen, Matthew A. Wilson, Conner V. Hartwig, John F. |
description | The borylation of methylarenes with a silylborane reagent and a new iridium catalyst containing an electron‐deficient phenanthroline ligand selectively leads to benzylic boronate esters over the corresponding aryl boronate esters. |
doi_str_mv | 10.1002/chin.201551175 |
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subjects | boration catalysis catalysis, phase‐transfer catalysis hydroboration hydroboration, boration organo-boron compounds phase-transfer catalysis |
title | ChemInform Abstract: Iridium-Catalyzed Borylation of Primary Benzylic C-H Bonds Without a Directing Group: Scope, Mechanism, and Origins of Selectivity |
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