CuI-Catalyzed AzideâAlkyne Intramoleculari-to-(i+4) Side-Chain-to-Side-Chain Cyclization Promotes the Formation of Helix-Like Secondary Structures-Reference-Cited by-同舟云学术

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CuI-Catalyzed AzideâAlkyne Intramoleculari-to-(i+4) Side-Chain-to-Side-Chain Cyclization Promotes the Formation of Helix-Like Secondary Structures

Published:2010-01 Issue:3 Volume:2010 Page:446-457
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Scrima Mario,Le Chevalier-Isaad Alexandra,Rovero Paolo,Papini Anna Maria,Chorev Michael,D'Ursi Anna Maria

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.200901157/fullpdf

Reference35 articles.

1. Synthesis and Conformational Analysis of a Cyclic Peptide Obtained via i to i+4 Intramolecular Side-Chain to Side-Chain Azide−Alkyne 1,3-Dipolar Cycloaddition

2. Design of potent cyclic gonadotropin releasing hormone antagonists

3. CONSTRAINED PEPTIDES: MODELS OF BIOACTIVE PEPTIDES AND PROTEIN SUBSTRUCTURES

4. An All-Hydrocarbon Cross-Linking System for Enhancing the Helicity and Metabolic Stability of Peptides

5. Synthesis, biological activity and conformational analysis of cyclic GRF analogs

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