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Synthesis of cell-wall analogues of vancomycin-resistant enterococci using solid phase peptide synthesis

✍ Scribed by Younghoon R. Cho; Richard M.H. Entress; Dudley H. Williams


Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
238 KB
Volume
38
Category
Article
ISSN
0040-4039

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✦ Synopsis


A convenicn! melht~ for tile dirccl coupling of lithium D-lactate Io 2-chlorotrityl chloride resin enabled the rapid and efficient solid phase synthesis of bacteri~d cell-wall precursor analogues (depsipeptides) fimnd in vancomycin-resistant culcrococci (VRE).


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## Abstract In this paper we describe the synthesis of chiral peptide nucleic acids (PNAs) 1–3 using SPPS methodologies. Starting material for the monomer units was the commercially available amino acid ornithine. l‐ or D‐ornithine and the nucleobase thymine were linked by a carboxymethylene spacer