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卷 25, 期 26, 页码 4835-4839出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.3c01555
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In this report, we introduce a new strategy for the synthesis of difluorothiocyanate compounds through visible-light-induced, copper-catalyzed three-component thiocyanation of alkenes. This approach is versatile and can be extended to perfluorothiocyanate compounds and even complex molecules with drug/natural product skeletons. Mechanistic studies reveal that the copper complex plays a dual role as a photoredox catalyst for electron transfer and a cross-coupling catalyst for C-SCN bond formation.
In this report, we develop a new strategy for visible-light-induced,copper-catalyzed three-component difluoroalkyl thiocyanidation ofalkenes to construct a series of important difluorothiocyanate compounds.The new approach can also be applied to perfluorothiocyanate compounds,even target molecules containing drug/natural product skeletons. Mechanisticstudies provide that the copper complex plays a dual role, as boththe photoredox catalyst for electron transfer and the cross-couplingcatalyst for C-SCN bond formation.
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