Transition metal-catalyzed borylation of alkanes and arenes via C-H activation
Abstract
Since 1999, direct borylation of hydrocarbons catalyzed by a transition metal complex has been extensively studied by several groups and has become an economical, efficient, elegant, and environmentally benign protocol for the synthesis of a variety of organoboron compounds. Re-, Rh-, Ir- and Pd-catalyzed C -H borylation of alkanes, arenes and benzylic positions of alkylarenes by bis(pinacolato)diboron or pinacolborane provide alkyl-, aryl-, heteroaryl- and benzylboron compounds, respectively. In this review, seminal early works and exciting recent developments in the area of direct borylation of hydrocarbons via C -H activation are summarized.
Journal
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- Journal of Organometallic Chemistry
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Journal of Organometallic Chemistry 680 (1-2), 3-11, 2003-08-29
Elsevier
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Keywords
Details 詳細情報について
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- CRID
- 1050564288970171776
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- NII Article ID
- 120005438243
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- HANDLE
- 2115/56230
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- ISSN
- 0022328X
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- Text Lang
- en
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- Article Type
- journal article
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- Data Source
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- IRDB
- CiNii Articles