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Synthesis 2021; 53(11): 1955-1961
DOI: 10.1055/s-0040-1705998
DOI: 10.1055/s-0040-1705998
paper
Simple Synthesis of Substituted 3-Hydroxyfuran-2(5H)-ones
The reported study was funded by the Russian Foundation for Basic Research (RFBR; research project no 17-43-590653).
Abstract
A convenient and facile approach to functionalized 4-substituted 3,5-dihydroxy-5-(trichloromethyl)furan-2(5H)-ones was developed. This method is based on regioselective synthesis of novel furan-2,3-diones containing the trichloromethyl group and subsequent hydrolysis. The structures of compounds were unambiguously confirmed by single-crystal X-ray diffraction.
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0040-1705998.
- Supporting Information
Publication History
Received: 17 October 2020
Accepted after revision: 19 November 2020
Article published online:
11 January 2021
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For the introduction of a trichloromethyl group, see:
For the cyclization of 1, 3-dicarbonyl compounds with oxalyl chloride, see:
For the opening of a furandione cycle, see: