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Transition-Metal-Free Borylation of Aryl Bromide Using a Simple Diboron Source

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Author(s)
Lim, TaehoRyoo, Jeong YupHan, Min Su
Type
Article
Citation
JOURNAL OF ORGANIC CHEMISTRY, v.85, no.16, pp.10966 - 10972
Issued Date
2020-08
Abstract
In this study, we developed a simple transition-metal-free borylation reaction of aryl bromides. Bis-boronic acid (BBA), was used, and the borylation reaction was performed using a simple procedure at a mild temperature. Under mild conditions, aryl bromides were converted to arylboronic acids directly without any deprotection steps and purified by conversion to trifluoroborate salts. The functional group tolerance was considerably high. The mechanism study suggested that this borylation reaction proceeds via a radical pathway.
Publisher
AMER CHEMICAL SOC
ISSN
0022-3263
DOI
10.1021/acs.joc.0c01065
URI
https://scholar.gist.ac.kr/handle/local/12025
Appears in Collections:
Department of Chemistry > 1. Journal Articles
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