@article{00b32b18ce83470e98a169f9f55ef948,
title = "Copper-Catalyzed Single C-H Amination of 8-Aminoquinoline-Directed Ferrocenes",
abstract = "An unprecedented copper-catalyzed C-H monoamination of ferrocenes directed by an 8-Aminoquinoline amide directing group is described. This reaction proceeds in the presence of a catalytic amount of copper catalyst with both cyclic and acyclic amines to afford the various aminoferrocenes. The C-H amination of ortho-substituted ferroceneamides was also achieved, enabling rapid access to multisubstituted ferrocenes that are useful for developing new functional molecules. ",
author = "Kazuya Kanemoto and Nao Horikawa and Shun Hoshino and Yuichiro Tokoro and Fukuzawa, {Shin Ichi}",
note = "Funding Information: This work was supported by the Kato Memorial Bioscience Foundation (K.K.), Tokyo Biochemical Research Foundation (K.K.), Takahashi Industrial and Economic Research Foundation (K.K.), Meiji Seika Award in Synthetic Organic Chemistry, Japan (K.K.), JSPS KAKENHI Grant No. JP19K23637 (Research Activity Start-up; K.K.), JP20K15288 (Young Scientists; K.K.), JP21K05415 (Scientific Research (C); S.F.), and The Institute of Science and Engineering, Chuo University. Publisher Copyright: {\textcopyright} 2021 American Chemical Society. All rights reserved.",
year = "2021",
month = jul,
day = "2",
doi = "10.1021/acs.orglett.1c01294",
language = "English",
volume = "23",
pages = "4966--4970",
journal = "Organic Letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "13",
}