期刊
ORGANIC LETTERS
卷 23, 期 7, 页码 2821-2825出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.1c00809
关键词
-
资金
- National Natural Science Foundation of China [21602096]
A benzoic acid-promoted C2-H borylation of indoles with pinacolborane is developed, providing a prompt route toward the synthesis of diverse C2-functionalized indoles. Preliminary mechanistic studies suggest that BH3-related borane species formed via the decomposition of pinacolborane may be the probable catalyst.
A benzoic acid-promoted C2-H borylation of indoles with pinacolborane to afford C2-borylated indoles is developed. Preliminary mechanistic studies indicate BH3-related borane species formed via the decomposition of pinacolborane to be the probable catalyst. This transformation provides a prompt route toward the synthesis of diverse C2-functionalized indoles.
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