Functionalization of Organotrifluoroborates via Cu-Catalyzed C-N Coupling Reaction

Authors
Lee, Jung-HyunKim, HeejinKim, TaejungSong, Jung HoKim, Won-SukHam, Jungyeob
Issue Date
2013-01-20
Publisher
KOREAN CHEMICAL SOC
Citation
BULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.34, no.1, pp.42 - 48
Abstract
Potassium N-heterobiaryltrifluoroborates were successfully prepared via a selective Cu-catalyzed C-N coupling reaction. The BF3K moiety was well tolerated under the reaction conditions involving CuI and dimethylethylenediamine (DMEDA) in the presence of DMSO. The Pd-catalyzed Suzuki-Miyaura cross couplings of potassium N-heterobiaryltrifluoroborates with bromoarenes were studied to prepare the N-heterotriaryl compounds. Moreover, homocoupling, iodination, and hydroxylation of potassium N-heterobiaryltrifluoroborates provided the corresponding products in high yields.
Keywords
ARYLBORONIC ACID; CUPRIC ACETATE; MESSENGER-RNA; ARYL IODIDES; ARYLATION; CELECOXIB; PYRAZOLES; LIGANDS; DPC-423; SALTS; ARYLBORONIC ACID; CUPRIC ACETATE; MESSENGER-RNA; ARYL IODIDES; ARYLATION; CELECOXIB; PYRAZOLES; LIGANDS; DPC-423; SALTS; Organotrifluoroborate; Potassium N-heterobiaryltrifluoroborates; Cu-catalyzed C-N coupling; Chan-Lam coupling; N-Heterobiarene
ISSN
0253-2964
URI
https://pubs.kist.re.kr/handle/201004/128442
DOI
10.5012/bkcs.2013.34.1.42
Appears in Collections:
KIST Article > 2013
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