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Synthesen in der Polymyxin-Reihe 1. Mitteilung. Synthese eines Pentapeptid-Fragmentes

✍ Scribed by K. Vogler; P. Lanz


Publisher
John Wiley and Sons
Year
1960
Tongue
German
Weight
771 KB
Volume
43
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

The protected pentapeptide formyl‐L‐leucyl‐N^γ^‐benzyloxycarbonyl‐L‐α,γ‐diaminobutyryl‐N^γ^‐benzyloxycarbonyl‐L‐α,γ‐diaminobutyryl‐L‐threonyl‐N^γ^‐benzyloxycarbonyl‐L‐α,γ‐diaminobutyric acid, a sequence which is known to occur in the polymyxins, has been synthesized. Different coupling methods including the azide route lead to the same end product, with the same optical rotation. We therefore believe our pentapeptide to be optically pure.


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Isle? zum 60. Geburtstag gewidmet (6. V. 70) 12. Mitteilung') Summary. The synthesis of the cycloheptapeptide XI (Figure l), corresponding to the structurc proposed by T . Suzuki et al. for the antibiotic Polymyxin D, is reported. This synthetic compound proved to be identical in all respects with n