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- W2041569494 endingPage "420" @default.
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- W2041569494 abstract "The modular assembly of heparin oligosaccharides requires glucosamine building blocks with amine protecting groups for α-selective glycosylations that can be readily removed. The synthesis of N-4-nitrobenzensulphonamide (nosyl)- and N-2,4-dinitrophenyl (DNP)-protected glucosamine building blocks and their evaluation as glycosylating agents is described. The N-nosyl-protected glucosamine building blocks were challenging to prepare and their glycosylations resulted in inseparable mixtures of products. The N-DNP-protected glucosamines, however, were readily synthesized and resulted in α-selective couplings to protected l-iduronic acid derivatives." @default.
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- W2041569494 date "2009-09-01" @default.
- W2041569494 modified "2023-09-28" @default.
- W2041569494 title "Synthesis of Differentially Protected Glucosamine Building Blocks and Their Evaluation as Glycosylating Agents" @default.
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- W2041569494 doi "https://doi.org/10.1080/07328300903105108" @default.
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