2 article(s) from Du, Yunfei
Biologically active chromone derivatives.
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Methods for the synthesis of chromones via dehydrogenative oxidation of chromanones.
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Substrate scope studies. Reaction conditions: 1 (1.0 mmol), PhIO (2.0 mmol), DMF (6 mL), rt. Isolat...
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Control experiments for mechanistic studies.
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Proposed reaction mechanism.
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Application of the reported method to the synthesis of frutinone A.
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Beilstein J. Org. Chem. 2019, 15, 2958–2965, doi:10.3762/bjoc.15.291
Representative pharmaceutical agents bearing the CF3 group.
The structures of the Togni reagents 1-(trifluoromethyl)-1,2-benziodoxol-3(1H)-one (1) and trifluor...
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Our previous hypervalent iodine-mediated synthesis of 2H-azirine compounds.
Study on the presumed Togni reagent 1-mediated trifluoromethylation followed by PhIO-mediated aziri...
Togni reagent/PhIO-mediated one-pot synthesis of β-trifluoromethyl 2H-azirines. Reaction conditions...
Control study with TEMPO.
Proposed mechanism for the Togni reagent-mediated trifluoromethylation of enamines.
Beilstein J. Org. Chem. 2018, 14, 1452–1458, doi:10.3762/bjoc.14.123
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