| Literature DB >> 27101475 |
Shun-Jiang Yao1, Zhi-Hui Ren1, Yao-Yu Wang1, Zheng-Hui Guan1.
Abstract
A simple and efficient protocol for the fluoroacetylation of indoles is reported. The reaction uses fluorinated acetic acids as the fluoroacetylation reagents to synthesize diverse fluoromethyl indol-3-yl ketones in good yields under catalyst- and additive-free conditions. In addition, the only byproduct is water in this transformation. The synthetic utility of this reaction was also demonstrated by the concise synthesis of α-(trifluoromethyl)(indol-3-yl)methanol and indole-3-carboxylic acid.Entities:
Year: 2016 PMID: 27101475 DOI: 10.1021/acs.joc.6b00580
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354