@article{db534c4bb883464eb7c44fa414143628,
title = "Nickel-catalysed decarbonylative borylation of aroyl fluorides",
abstract = "The first Ni(cod)2/PPh3 catalyst system has been established for decarbonylative borylation of aroyl fluorides with bis(pinacolato)diboron. A wide range of functional groups in the substrates were well tolerated. The ease of access of the starting aroyl fluorides indicates that these results might become an alternative to the existing decarbonylation events.",
author = "Zhenhua Wang and Xiu Wang and Yasushi Nishihara",
note = "Funding Information: This study was partly supported by ACT-C, JST Grant JPMJCR12YW, Japan. The authors gratefully thank Ms Megumi Kosaka and Mr Motonari Kobayashi at the Department of Instrumental Analysis, Advanced Science Research Centre, Okayama University for the measurements of elemental analyses and the SC-NMR Laboratory of Okayama University for the NMR spectral measurements. Publisher Copyright: {\textcopyright} The Royal Society of Chemistry.",
year = "2018",
doi = "10.1039/c8cc08504h",
language = "English",
volume = "54",
pages = "13969--13972",
journal = "Chemical Communications",
issn = "1359-7345",
publisher = "Royal Society of Chemistry",
number = "99",
}