Issue 9, 1997

New methoxy-substituted 9-phenylxanthen-9-ylamine linkers for the solid phase synthesis of protected peptide amides

Abstract

New methoxy-substituted 9-phenylxanthen-9-ylamine linkers are described for the solid phase synthesis of peptide amides via the Fmoc strategy; depending on the cleavage conditions, the peptide amides can be cleaved rapidly and in high purity in their protected or deprotected forms.

Article information

Article type
Paper

Chem. Commun., 1997, 849-850

New methoxy-substituted 9-phenylxanthen-9-ylamine linkers for the solid phase synthesis of protected peptide amides

M. Meisenbach, H. Echner and W. Voelter, Chem. Commun., 1997, 849 DOI: 10.1039/A700895C

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