AN IMPROVED SYNTHESIS OF N∊-FMOC-L-LYSINE AND Nδ-FMOC-L-ORNITHINE

M Henczi, DF Weaver

Index: Henczi, Maria; Weaver, Donald F. Organic Preparations and Procedures International, 1994 , vol. 26, # 5 p. 578 - 580

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Citation Number: 8

Abstract

The selective introduction of a readily removed mine protecting group into the side-chnin of a dibasic amino acid petinits the synthetically desirable objective of sidechain modification to a" nonnntural/atypical" residue following the synthesis of the backbone. The 9- fluorenylmethoxycarhonyl (Ftnoc) group, which is easily deblocked under mild basic conditions' and is compatihle with either t-

Epimerization of peptide nucleic acids analogs during solid-phase synthesis: optimization of the coupling conditions for increasing the optical purity

[Corradini, Roberto; Sforza, Stefano; Dossena, Arnaldo; Palla, Gerardo; Rocchi, Raniero; Filira, Ferdinando; Nastri, Flavia; Marchelli, Rosangela Journal of the Chemical Society. Perkin Transactions 1, 2001 , # 20 p. 2690 - 2696]

AN IMPROVED SYNTHESIS OF N∊-FMOC-L-LYSINE AND Nδ-FMOC-L-ORNITHINE

Abstract

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