Nickel-Catalyzed Direct Coupling of Heteroarenes
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- Yamaguchi Junichiro
- Graduate School of Science, Nagoya University
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- Muto Kei
- Graduate School of Science, Nagoya University
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- Amaike Kazuma
- Graduate School of Science, Nagoya University
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- Yamamoto Takuya
- Graduate School of Science, Nagoya University
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- Itami Kenichiro
- Graduate School of Science, Nagoya University Institute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University
Bibliographic Information
- Other Title
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- ニッケル触媒を用いたヘテロ芳香族化合物の直接的カップリング
- ニッケル ショクバイ オ モチイタ ヘテロ ホウコウゾク カゴウブツ ノ チョクセツテキ カップリング
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Abstract
Nickel-catalyzed cross-coupling reactions have recently been receiving significant attention from the synthetic community as a way to construct carbon-carbon or carbon-heteroatom bonds, because nickel catalysts are less expensive and less toxic than palladium catalysts.<br>We herein describe our recent developments in nickel-catalyzed biaryl coupling methodology, along with mechanistic studies and applications to the synthesis of natural products and pharmaceuticals. In particular, we focus on nickel-catalyzed direct coupling reactions in which “unreactive” bonds such as C-H, C-O, and C-C bonds are converted into biaryl moieties.
Journal
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- Journal of Synthetic Organic Chemistry, Japan
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Journal of Synthetic Organic Chemistry, Japan 71 (6), 576-587, 2013
The Society of Synthetic Organic Chemistry, Japan
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Keywords
Details 詳細情報について
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- CRID
- 1390282680317387264
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- NII Article ID
- 10031178156
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- NII Book ID
- AN0024521X
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- COI
- 1:CAS:528:DC%2BC3sXpsVGis7g%3D
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- ISSN
- 18836526
- 00379980
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- NDL BIB ID
- 024687246
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
- KAKEN
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- Abstract License Flag
- Disallowed
