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- W2002520200 abstract "A series of 3-alkoxy(phenyl)thiophosphorylamido-2-(per-O-acetylglycosyl-1′-imino)thiazolidine-4-one derivatives were prepared by the reaction of 1-alkoxy(phenyl)thiophosphoryl-4-(per-O-acetylglycosyl) thiosemicarbazides with ethyl bromoacetate. 1H/13C HMBC measurements corroborated by X-ray crystallographic results revealed the exclusive regioselectivity of these ring closures toward the N-2 position of the thiosemicarbazide moiety. The bioactivity data of 3a–k suggest that the thiazolidine-4-one ring is critical for the herbicidal and fungicidal activities." @default.
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- W2002520200 date "2009-07-01" @default.
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- W2002520200 title "Regioselective synthesis of novel 3-alkoxy (phenyl) thiophosphorylamido-2-(per-O-acetylglycosyl-1′-imino)thiazolidine-4-one derivatives from O-alkyl N4-glycosyl(thiosemicarbazido)phosphonothioates" @default.
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- W2002520200 doi "https://doi.org/10.1016/j.carres.2009.03.027" @default.
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