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- W4313237410 endingPage "908" @default.
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- W4313237410 abstract "Herein, we report a new and highly efficient approach for synthesizing congested α-thioamides under mild reaction conditions (mild base, room temperature, and short duration) using α-halo hydroxamates as direct alkylating agents. The reaction works well with both (hetero)aryl and alkyl thiols, tolerating a broad functional group and diverse substrate scope, including benzeneselenol for selenoether construction. The strategy enables efficient synthesis of biologically relevant 1,4 benzothiazinone and 4,1-benzothiazepinone cores, along with various other functionalized sulfur-based scaffolds of biological importance." @default.
- W4313237410 created "2023-01-06" @default.
- W4313237410 creator A5038000765 @default.
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- W4313237410 creator A5071923033 @default.
- W4313237410 creator A5086936506 @default.
- W4313237410 date "2022-12-28" @default.
- W4313237410 modified "2023-09-25" @default.
- W4313237410 title "Access to Sterically Hindered Thioethers (α-Thioamides) Under Mild Conditions Using α-Halohydroxamates: Application toward 1,4-Benzothiazinones and 4,1-Benzothiazepinones" @default.
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- W4313237410 doi "https://doi.org/10.1021/acs.joc.2c02274" @default.
- W4313237410 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36576371" @default.
- W4313237410 hasPublicationYear "2022" @default.
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