Synthesis of Heterocycle-Bridged Peptidic Macrocycles through 1,3-Diyne Transformations-Reference-Cited by-同舟云学术

Synthesis of Heterocycle-Bridged Peptidic Macrocycles through 1,3-Diyne Transformations

Published:2016-11-21 Issue:35 Volume:2016 Page:5807-5812
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Verlinden Steven¹,Ballet Steven¹,Verniest Guido¹^ORCID

Affiliation:

1. Research group of Organic Chemistry; Department of Chemistry and Department of Bio-engineering Sciences; Faculty of Science and Bio-engineering Sciences; Vrije Universiteit Brussel (VUB); Pleinlaan 2 1050 Brussels Belgium

Funder

Vrije Universiteit Brussel

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference34 articles.

1. Oxidative α,ω-diyne coupling as an approach towards novel peptidic macrocycles

2. Glaser oxidative coupling on peptides: Stabilization of β-turn structure via a 1,3-butadiyne constraint

3. Expanding the scope of alkyne-mediated bioconjugations utilizing unnatural amino acids

4. Development and Optimization of Glaser-Hay Bioconjugations

5. Development and Optimization of Glaser-Hay Bioconjugations

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