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Issue 13, 1978
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A mild procedure for solid phase peptide synthesis: use of fluorenylmethoxycarbonylamino-acids

Abstract

Use of base-labile N-fluorenylmethoxycarbonylamino-acids, t-butyl based side chain protecting groups, and a p-alkoxybenzyl ester resin linkage provides a simple, rapid, and exceptionally mild strategy in solid phase peptide synthesis.

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Article information


J. Chem. Soc., Chem. Commun., 1978, 537-539
Article type
Paper

A mild procedure for solid phase peptide synthesis: use of fluorenylmethoxycarbonylamino-acids

E. Atherton, H. Fox, D. Harkiss, C. J. Logan, R. C. Sheppard and B. J. Williams, J. Chem. Soc., Chem. Commun., 1978, 537
DOI: 10.1039/C39780000537

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