Journal
RSC ADVANCES
Volume 8, Issue 25, Pages CP56-CP61Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ra01381k
Keywords
-
Categories
Funding
- Science and Technology Planning Project of Guangdong Province [2015A020211039]
- Young Innovative Talents in Higher Education of Guangdong [2015KQNCX134]
- National Natural Science Foundation of China [30701051]
- Scientific Research Project for Guangzhou Municipal Colleges and Universities [1201610139]
Ask authors/readers for more resources
A highly efficient room-temperature borylation strategy of aryl chlorides is described. Utilizing Buchwald's second-generation preformed catalyst, boronate esters were obtained for a wide range of substrates in high yield. The method was also applied to Suzuki-Miyaura cross-coupling reaction in a one-pot two-step sequential manner, providing a facile and convenient access to the direct synthesis of biaryl compounds from aryl chlorides.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available