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Aromatic C-H amination: a radical approach for adding new functions into biology- and materials-oriented aromatics.
Murakami, Kei; Perry, Gregory J P; Itami, Kenichiro.
Afiliação
  • Murakami K; Institute of Transformative Bio-Molecules (WPI-ITbM) and Graduate School of Science, Nagoya University, Chikusa, Nagoya 464-8602, Japan. murakami@chem.nagoya-u.ac.jp itami@chem.nagoya-u.ac.jp.
  • Perry GJP; Institute of Transformative Bio-Molecules (WPI-ITbM) and Graduate School of Science, Nagoya University, Chikusa, Nagoya 464-8602, Japan. murakami@chem.nagoya-u.ac.jp itami@chem.nagoya-u.ac.jp.
  • Itami K; Institute of Transformative Bio-Molecules (WPI-ITbM) and Graduate School of Science, Nagoya University, Chikusa, Nagoya 464-8602, Japan. murakami@chem.nagoya-u.ac.jp itami@chem.nagoya-u.ac.jp and JST, ERATO, Itami Molecular Nanocarbon Project, Nagoya University, Chikusa, Nagoya 464-8602, Japan.
Org Biomol Chem ; 15(29): 6071-6075, 2017 Aug 07.
Article em En | MEDLINE | ID: mdl-28681886
ABSTRACT
C-H amination is the most powerful method to directly add nitrogen functionalities into a variety of arenes including biology- and materials-oriented molecules. Recent developments in aromatic C-H amination chemistry have enabled the conversion of unactivated arenes into a range of arylamine derivatives without using directing groups or excess amounts of arenes. The key for such successful transformations is the catalytic generation of nitrogen or arene radical intermediates. In this perspective, we discuss recent developments in the radical C-H amination of aromatic molecules. We believe the resulting arylamines, which are hitherto difficult to access, will exhibit unexplored functions for biological and materials application.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article