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- W2936298178 endingPage "4704" @default.
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- W2936298178 abstract "N-Heterocyclic carbene (NHC)-catalyzed diastereoselective synthesis of multisubstituted sulfenylated indanes has been developed. In the presence of 1 mol% NHC, various thiols underwent the sulfa-Michael-Michael cascade reaction with benzenedi(enones) efficiently to form the carbon-sulfur bond and construct sulfenylated indanes in good to excellent yields with high diastereoselectivity. In addition, the NHC-catalyzed sulfa-Michael-aldol cascade reaction between o-formyl chalcone and thiols has also been demonstrated to afford sulfenylated indanes with a free hydroxyl group in moderate yields and good diastereoselectivity." @default.
- W2936298178 created "2019-04-25" @default.
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- W2936298178 creator A5074529359 @default.
- W2936298178 creator A5074557688 @default.
- W2936298178 creator A5078597900 @default.
- W2936298178 date "2019-01-01" @default.
- W2936298178 modified "2023-10-15" @default.
- W2936298178 title "N-Heterocyclic carbene-catalyzed diastereoselective synthesis of sulfenylated indanes <i>via</i> sulfa-Michael–Michael (aldol) cascade reactions" @default.
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- W2936298178 doi "https://doi.org/10.1039/c9ob00210c" @default.
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- W2936298178 hasPublicationYear "2019" @default.
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