@article{f6ada92b6b6f41208a4a9fa173d9c023,
title = "Palladium-catalysed direct thiolation and selenation of aryl C-H bonds assisted by directing groups",
abstract = "Direct chalcogenation of aryl C-H bonds has attracted a lot of attention because arylcharcogen compounds represent useful building blocks in bioactive molecules and functional organic materials. Very recently, chelate-assisted intermolecular direct thiolation and selenation have been developed using various transition-metal catalysts such as palladium, rhodium, nickel, copper and ruthenium. In addition, an appropriate choice of directing group can be used to control the reaction sites. This highlight review focuses on the recent advances in catalytic C-H chalcogenation.",
author = "Masayuki Iwasaki and Yasushi Nishihara",
note = "Funding Information: The work presented herein was partially supported by ACT-C, JST and a Grant-in-Aid for Scientific Research (KAKENHI) (No. 16K17901) from JSPS. The authors gratefully thank Prof. Kiyohiko Nakajima (Aichi University of Education) for the X-ray analyses, Prof. Zhiping Li (Renmin University of China) for valuable discussions, Ms Megumi Kosaka and Mr Motonari Kobayashi (Department of Instrumental Analysis, Advanced Science Research Center, Okayama University) for the elemental analyses and the SC-NMR Laboratory (Okayama University) for the NMR spectral measurements. M. I. acknowledges financial support from Shionogi Award in Synthetic Organic Chemistry, Japan, Yazaki Memorial Foundation for Science and Technology, and Japan Prize Foundation. Publisher Copyright: {\textcopyright}2016 The Royal Society of Chemistry. Copyright: Copyright 2017 Elsevier B.V., All rights reserved.",
year = "2016",
doi = "10.1039/c6dt02167k",
language = "English",
volume = "45",
pages = "15278--15284",
journal = "Dalton Transactions",
issn = "1477-9226",
publisher = "Royal Society of Chemistry",
number = "39",
}