A nickel-catalyzed tandem reaction involving cyclic esterification/C-S bond formation for synthesizing 5-oxa-11-thia-benzofluoren-6-ones

A nickel-catalyzed tandem reaction involving cyclic esterification/C-S bond formation has been developed. Starting from samples containing 3-(2-hydroxy-phenyl)-acrylic acids with 2-halide-benzenethiols, versatile biologically active 5-oxa-11-thia-benzofluoren-6-one compounds were efficiently synthes...

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Veröffentlicht in:RSC advances 2020-07, Vol.1 (44), p.26414-26417
Hauptverfasser: Cai, Rongrong, Wei, Qicai, Xu, Runsheng
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Sprache:eng
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Zusammenfassung:A nickel-catalyzed tandem reaction involving cyclic esterification/C-S bond formation has been developed. Starting from samples containing 3-(2-hydroxy-phenyl)-acrylic acids with 2-halide-benzenethiols, versatile biologically active 5-oxa-11-thia-benzofluoren-6-one compounds were efficiently synthesized in good to high yields. This new methodology provides an economical approach toward C-S bond formation. A nickel-catalyzed tandem reaction involving cyclic esterification/C-S bond formation has been developed.
ISSN:2046-2069
2046-2069
DOI:10.1039/d0ra04367b