Issue 11, 1978

The mesitylene-2-sulphonyl group, an acidolytically removable NG-protecting group for arginine

Abstract

The mesitylene-2-sulphonyl (Mts) group attached at the guanidino function of arginine can be quantitatively cleaved by methanesulphonic acid, as well as trifluoromethanesulphonic acid and hydrogen fluoride; this new Arg(Mts) derivative was successfully applied to the synthesis of hypothalamic substance P.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 482-483

The mesitylene-2-sulphonyl group, an acidolytically removable NG-protecting group for arginine

H. Yajima, M. Takeyama, J. Kanaki and K. Mitani, J. Chem. Soc., Chem. Commun., 1978, 482 DOI: 10.1039/C39780000482

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