Abstract
Highly regioselective ruthenium-catalyzed direct benzylations through C-H bond cleavages were accomplished under remarkably mild, nonacidic reaction conditions, for which experimental studies suggested a S(E)Ar-type mechanism not to be operative.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Benzene Derivatives / chemical synthesis*
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Benzene Derivatives / chemistry*
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Catalysis
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Molecular Structure
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Ruthenium / chemistry*
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Stereoisomerism
Substances
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Benzene Derivatives
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Ruthenium