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Peptide modification by incorporation of α-trifluoromethyl substituted α-amino acids

✍ Scribed by Klaus Burger; Norbert Sewald; Christian Schierlinger; Kerstin Mütze; Liza C. Seymour


Publisher
Elsevier Science
Year
1991
Tongue
English
Weight
23 KB
Volume
54
Category
Article
ISSN
0022-1139

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✦ Synopsis


a-Trifluoromethyl a-amino acids are potentially intaresting candidates for modification of biological active peptides. We report on new strategies for asymmetric synthesis of a-trifluoromethyl substituted a-amino acids. Approaches to amino group protection and carboxylic group activation are presented.


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Proteolytically stable peptides by incor
✍ Beate Koksch; Norbert Sewald; Hans-Jörg Hofmann; Klaus Burger; Hans-Dieter Jakub 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 234 KB 👁 1 views

A series of model peptides containing a-trifluoromethyl-substituted amino acids in five different positions relative to the predominant cleavage site of the serine protease a-chymotrypsin was synthesized by solution methods to investigate the influence of a-Tfm substitution on the proteolytic stabil