作者:St. Guttmann、J. Pless、Ed. Sandrin、P.-A. Jaquenoud、H. Bossert、H. Willems
DOI:10.1002/hlca.19680510518
日期:1968.7.10
AbstractA total synthesis of hog thyrocalcitonin is described. A protected C‐terminal tridecapeptide amid (20–32) was coupled with a protected central decapeptide (10–19), and the resulting protected tricosapeptide amide (10–32) was reacted with the N‐terminal protected nonapeptide (1–9). After elimination of the protective groups, a free dotriacontapeptide amide was obtained whose physical, chemical and biological behaviour was indistinguishable from that of the natural hormone.