## Abstract Durch die MERRIFIELD‐Synthese des Oktapeptid‐Derivats Phe‐Val‐Asn‐Gln‐His(Bzl)‐Leu‐Cys(R)‐Gly wurden die S‐Schutzgruppen R gleich Benzyl (Bzl), __p__‐Methoxybenzyl (Mbzl), Diphenylmethyl (Dpm), Trityl (Trt), Tetrahydropyranyl (Thp), Benzylthiomethyl (Btm), äthylcarbamoyl (Ec), Benzyloxy
✦ LIBER ✦
Synthese eines neuen Derivats der Insulinsequenz B1–8 mit verbesserter Löslichkeit
✍ Scribed by H. R. Bosshard
- Publisher
- John Wiley and Sons
- Year
- 1971
- Tongue
- German
- Weight
- 628 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The synthesis of the protected octapeptide N‐t‐butoxycarbonyl‐phenylalanyl‐valylasparaginyl‐glutaminyl‐N^im^‐tritylhistidyl‐leucyl‐S‐benzhydrylcysteinyl‐glycine‐hydrazide L
, corresponding to the amino‐terminal sequence of the insulin B‐chain, is described. Up to the protected octapeptide all intermediates have greatly improved solubility properties in neutral organic solvents in comparison with other synthetic derivatives of the same sequence.
📜 SIMILAR VOLUMES
MERRIFIELD-synthese der insulinsequenz B
✍
Hammerström, Von Knut ;Lunkenheimer, Winfried ;Zahn, Helmut
📂
Article
📅
1970
🏛
Wiley (John Wiley & Sons)
⚖ 537 KB