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Elsevier, Tetrahedron Letters, 34(44), p. 6413-6416, 2003

DOI: 10.1016/s0040-4039(03)01586-7

Wiley-VCH Verlag, ChemInform, 47(34), 2003

DOI: 10.1002/chin.200347182

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Synthesis of a New Conformationally Constrained Glycoamino Acid Building Block.

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This paper is available in a repository.

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Abstract

The synthesis of a suitably protected β-d-glucopyranosyl-(S)-α-methylserine derivative—a new conformationally constrained glycosylated quaternary amino acid analogue of β-d-glucopyranosyl-l-serine—is described. This compound can be used as an attractive building block for the synthesis of new, constrained glycopeptides.