The Use of Intermediates with Preformed Disulfide Bridge for the Synthesis of Oxytocin and Deamino‐oxytocin
- 1 November 1972
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 55 (8) , 2854-2860
- https://doi.org/10.1002/hlca.19720550817
Abstract
The disulfide‐bridged hexapeptides 6a and 6b have been prepared from benzyl‐protected intermediates. Coupling of 6a and 6b with prolyl‐leucyl‐glycine amide afforded deamino‐oxytocin (7a) and the protected oxytocin derivative 7b, respectively; the latter was converted to oxytocin (7c) by removal of the Boc protecting group.Keywords
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