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- W2950659664 abstract "A palladium-catalyzed reaction has been applied toward the synthesis of divalent carbohydrate derivatives, which showed excellent lectin cross-linking abilities. The procedure, which involves copper(I) iodide and dichlorobis(triphenylphosphine)palladium(II)-catalyzed head-to-head coupling of prop-2-ynyl glycosides, is very efficient affording symmetrically conjugated carbohydrates containing 1,3-diynes in excellent yields. The reactions proceeded rapidly and efficiently at room temperature without the need for added oxidizing agents." @default.
- W2950659664 created "2019-06-27" @default.
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- W2950659664 date "2004-09-30" @default.
- W2950659664 modified "2023-10-18" @default.
- W2950659664 title "Palladium-Mediated Oxidative Homocoupling of Prop-2-ynyl Glycosides: Application Toward the Synthesis of Symmetrical Conjugated Sugar Diynes" @default.
- W2950659664 doi "https://doi.org/10.1055/s-2001-14903" @default.
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