scispace - formally typeset
Journal ArticleDOI

Eine neue Methode zur Synthese von Peptiden: Aktivierung der Carboxylgruppe mit Dicyclohexylcarbodiimid unter Zusatz von 1‐Hydroxy‐benzotriazolen

Wolfgang König, +1 more
- 01 Mar 1970 - 
- Vol. 103, Iss: 3, pp 788-798
TLDR
In this article, the authors show that 1-Hydroxy-benzotriazol and 1-hydroxy-acetyl carbodiimid-methode eignen sich als Zusatze bei der Dicyclohexylcarbodiimids-Methode zur Synthese von Peptiden, verhindern die N-Acyl-harnstoffbildung and fuhren in hoher Ausbeute.
Abstract
1-Hydroxy-benzotriazol sowie verschiedene kernsubstituierte 1-Hydroxy-benzotriazole eignen sich als Zusatze bei der Dicyclohexylcarbodiimid-Methode zur Synthese von Peptiden. Ihr Einflus auf die Racemisierung bei Peptidsynthesen wurde unter Anwendung des gaschromatographischen Racemisierungstests von Weygand u. Mitarbb.2) untersucht. Die neuen Zusatze senken die Racemisierung, verhindern die N-Acyl-harnstoffbildung und fuhren in hoher Ausbeute zu sehr reinen Peptiden.

read more

Citations
More filters
Journal ArticleDOI

Supramolecular hydrogel capsules based on PEG: a step toward degradable biomaterials with rational design.

TL;DR: Reversion of the supramolecular polymer cross-linking allows the microcapsules to be degraded at mild conditions with no effect on the viability of the encapsulated and released cells.
Journal ArticleDOI

Der Adamantyl‐(1)‐oxycarbonyl‐Rest als Schutzgruppe für die Guanidinofunktion des Arginins

Georg Jäger, +1 more
- 01 Jun 1970 - 
TL;DR: The 1-Adamantyloxycarbonyl Residue as Blocking Group for the Guanidino Function of Arginine as mentioned in this paper was introduced in high yield into the guanidino function by reaction of Nα-protected arginine with 1-adamantyl chloroformate.
Journal ArticleDOI

Heptanuclearity in nickel(II) chemistry: preparation, characterization, crystal structure and magnetic properties of [Ni7(OH)2(acac)8(btaO)4(H2O)2] (btaO−=the 1-hydroxybenzotriazolate ion)

TL;DR: In this paper, the structure of 4·MeCN·0.9H2O was determined by single-crystal X-ray crystallography, and the heptanuclear assembly was held together by two μ3 hydroxo ligands, two terminal H2O molecules, four chelating acac− groups, two μ2 acac+ groups, four acac-groups, two µ2 acAC− groups and two µ3 acac − groups.
Journal ArticleDOI

N-terminal myristylation of HBV preS1 domain enhances receptor recognition.

TL;DR: HBV-receptor binding assays performed with plasma membranes preparations from the hepatocyte carcinoma cell line HepG2 clearly showed that the preS1[1-119] domain recognizes the HBV receptor, and confirmed that binding is occurring through the 21-47 region, suggesting that the conformational transitions induced in thePreS1 moiety by fatty acid post-translational modification are important for efficient attachment of viral particles to HBV receptors.
Journal ArticleDOI

Intermolecular stabilisation of the β-sheet conformation in dipeptides

TL;DR: Dipeptides are stabilised in the β-sheet conformation by three-point binding through hydrogen bonds to 3-aminopyrazole binding sites.
References
More filters
Related Papers (5)