@article{2f1ae1b8957f4a80bfc13b48b681d667,
title = "Palladium-catalyzed borylation of aryl (pseudo)halides and its applications in biaryl synthesis",
abstract = "A facile and efficient palladium-catalyzed borylation of aryl (pseudo)halides at room temperature has been developed. Arylboronic esters were expeditiously assembled in good yields and with a broad substrate scope and good functional group compatibility. This approach has been successfully applied to the one-pot two-step borylation/Suzuki-Miyaura cross-coupling reaction, providing a concise access to biaryl compounds from readily available aryl halides. Furthermore, a parallel synthesis of biaryl analogs is accomplished at room temperature using the strategy, which enhances the practical usefulness of this method.",
keywords = "Aryl (pseudo)halides, Biaryl synthesis, Palladium-catalyzed borylation, Suzuki-Miyaura cross coupling",
author = "Hong Ji and Jianghong Cai and Nana Gan and Zhaohua Wang and Liyang Wu and Guorong Li and Tao Yi",
note = "Funding Information: The research was funded by the National Natural Science Foundation of China, the Science and Technology Department of Guangdong Province, Guangzhou Funding Information: We are grateful for financial support from the National Natural Science Foundation of China (No. 30701051), the Science and Technology Planning Project of Guangdong Province (2015A020211039), Natural Science Foundation of Guangdong Province (2018A0303130139), Scientific Research Project for Guangzhou Municipal Colleges and Universities (1201610139, 1201630263), Project for Young Innovative Talents in the Universities of Guangdong (2015KQNCX134) and Ph.D. Early Development Program of Guangzhou Medical University (2015C02). Publisher copyright: {\textcopyright} The Author(s) 2018 ",
year = "2018",
month = dec,
day = "19",
doi = "10.1186/s13065-018-0510-6",
language = "English",
volume = "12",
journal = "Chemistry Central Journal",
issn = "1752-153X",
publisher = "Chemistry Central",
}