Synthesis of the amino-terminal decapeptide of human calcitonin, in which the disulfide bond is replaced by a thioether group

Z Procházka, K Jošt

Index: Prochazka; Jost Collection of Czechoslovak Chemical Communications, 1980 , vol. 45, # 4 p. 1305 - 1314

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Citation Number: 9

Abstract

Abstract A fully protected amino-terminal decapeptide Ib with the sequence of human calcitonin, in which the SS bridge was replaced by the S-CH 2 group (a so-called 7-carba- analogue), was synthetized mainly by the stepwise method. The cyclization of the linear decapeptide was performed by means of active ester.