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- Kei Murakami
- Institute of Transformative Bio-Molecules (WPI-ITbM) and Graduate School of Science, and ‡JST-ERATO, Itami Molecular Nanocarbon Project, Nagoya University, Chikusa, Nagoya 464-8602, Japan
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- Shuya Yamada
- Institute of Transformative Bio-Molecules (WPI-ITbM) and Graduate School of Science, and ‡JST-ERATO, Itami Molecular Nanocarbon Project, Nagoya University, Chikusa, Nagoya 464-8602, Japan
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- Takeshi Kaneda
- Institute of Transformative Bio-Molecules (WPI-ITbM) and Graduate School of Science, and ‡JST-ERATO, Itami Molecular Nanocarbon Project, Nagoya University, Chikusa, Nagoya 464-8602, Japan
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- Kenichiro Itami
- Institute of Transformative Bio-Molecules (WPI-ITbM) and Graduate School of Science, and ‡JST-ERATO, Itami Molecular Nanocarbon Project, Nagoya University, Chikusa, Nagoya 464-8602, Japan
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説明
Azines, which are six-membered aromatic compounds containing one or more nitrogen atoms, serve as ubiquitous structural cores of aromatic species with important applications in biological and materials sciences. Among a variety of synthetic approaches toward azines, C-H functionalization represents the most rapid and atom-economical transformation, and it is advantageous for the late-stage functionalization of azine-containing functional molecules. Since azines have several C-H bonds with different reactivities, the development of new reactions that allow for the functionalization of azines in a regioselective fashion has comprised a central issue. This review describes recent advances in the C-H functionalization of azines categorized as follows: (1) S
収録刊行物
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- Chemical Reviews
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Chemical Reviews 117 (13), 9302-9332, 2017-04-26
American Chemical Society (ACS)