@article{bc57b08fcaeb463f99bae99314a40dfb,
title = "Efficient trifluoromethylation of C(sp2)-H functionalized α-oxoketene dithioacetals: a route to the regioselective synthesis of functionalized trifluoromethylated pyrazoles",
abstract = "An operationally simple approach for the regioselective construction of diversely substituted trifluoromethylated pyrazoles via nucleophilic trifluoromethylation of iodo-substituted α-oxoketene dithioacetals is described. X-ray crystallographic studies confirmed the trifluoromethylation as well as formation of a regioselective cyclized product. Furthermore, trifluoromethylated pyrazoles bearing thiomethyl groups may allow further functionalization and are of considerable interest in medicinal chemistry.",
author = "N. Sharma and N. Kumari and Chundawat, {T. S.} and S. Kumar and S. Bhagat",
note = "Funding Information: The authors are thankful to SERB, Department of Science & Technology, India for providing financial support and USIC, University of Delhi for providing instrumentation facilities. NS and NK are thankful to DST for INSPIRE Fellowship and UGC for SRF respectively. Publisher Copyright: {\textcopyright} The Royal Society of Chemistry.",
year = "2017",
doi = "10.1039/c7ra01130j",
language = "British English",
volume = "7",
pages = "10150--10153",
journal = "RSC Advances",
issn = "2046-2069",
publisher = "Royal Society of Chemistry",
number = "17",
}