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- W2128452385 startingPage "974" @default.
- W2128452385 abstract "A series of glycosyl hemiacetal derivatives have been transformed into thioglycosides and glycosyl thiols in a one-pot two-step reaction sequence mediated by Appel reagent (carbon tetrabromide and triphenylphosphine). 1,2- trans -Thioglycosides and β-glycosyl thiol derivatives were stereoselectively formed by the reaction of the in situ generated glycosyl bromides with thiols and sodium carbonotrithioate. The reaction conditions are reasonably simple and yields were very good." @default.
- W2128452385 created "2016-06-24" @default.
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- W2128452385 date "2013-05-22" @default.
- W2128452385 modified "2023-10-16" @default.
- W2128452385 title "Appel-reagent-mediated transformation of glycosyl hemiacetal derivatives into thioglycosides and glycosyl thiols" @default.
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- W2128452385 doi "https://doi.org/10.3762/bjoc.9.112" @default.
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