𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Building units for N-Backbone cyclic peptides. 2. Synthesis of protected N-(ω-thioalkylene) amino acids and their incorporation into dipeptide units

✍ Scribed by Gal Bilan; Chaim Gilon


Publisher
Elsevier Science
Year
1995
Tongue
French
Weight
636 KB
Volume
51
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Synthesis of differentially protected N-
✍ Diana Besser; Bettina Müller; Inge Agricola; Siegmund Reissmann 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 132 KB

Backbone cyclization has become an important method for generating or stabilizing the bioactive conformation of peptides without affecting the amino acid side-chains. Up to now, backbone cyclic peptides were mostly synthesized with bridges between N-amino- and N-carboxy-functionalized peptide bonds.

Synthesis of Alaninyl and N-(2-Aminoethy
✍ Thorsten Stafforst; Ulf Diederichsen 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 294 KB 👁 1 views

## Abstract Artificial amino acids carrying either the chromophore of the Green Fluorescent Protein (GFP) or a modification as their side chains have been synthesized: Boc‐protected alaninyl derivatives and Fmoc‐protected __N__‐(2‐aminoethyl)glycine‐functionalized amino acids were obtained and coul

Cover Picture: Synthesis of Alaninyl and
✍ Thorsten Stafforst; Ulf Diederichsen 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 134 KB 👁 2 views

## Abstract **The cover picture shows** a chromophore of the Green Fluorescent Protein, which undergoes fast internal conversion by rotation causing the quenching of its fluorescence in solution. In contrast, the intact protein shows a high fluorescence quantum yield and there is still a need to un