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• W2122839184 abstract "Sweetness & light! The glycosyloxyamine glycoside of calicheamicin was exploited to form neo-D-ribosides in one efficient chemoselective step. Assessment of the neoglycosides revealed only slight reductions in cytotoxicity or ability to cleave DNA compared to the parent aglycons. This study exposes a previously unrecognized method for efficient calicheamicin bioconjugation amenable to a wide range of cancer- selective targeting modalities." @default.
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• W2122839184 date "2011-02-23" @default.
• W2122839184 modified "2023-10-16" @default.
• W2122839184 title "Glycosyloxyamine Neoglycosylation: A Model Study Using Calicheamicin" @default.
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• W2122839184 doi "https://doi.org/10.1002/cmdc.201100028" @default.
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