Fmoc-Based Synthesis of Peptide Thioacids for Azide Ligations via 2-Cyanoethyl Thioesters-Reference-Cited by-同舟云学术

Fmoc-Based Synthesis of Peptide Thioacids for Azide Ligations via 2-Cyanoethyl Thioesters

Published:2012-09-19 Issue:19 Volume:14 Page:5038-5041
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Raz Richard¹,Rademann Jörg¹

Affiliation:

1. Medicinal Chemistry, Department of Pharmacy, Leipzig University, Brüderstr. 34, 01403 Leipzig, Germany, Leibniz Institute of Molecular Pharmacology (FMP), Robert-Rössle-Str. 10, 13125 Berlin, Germany, and Institute of Chemistry and Biochemistry, Free University Berlin, Takustr. 3, 14195 Berlin, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol302247h

Reference23 articles.

1. The Reaction of Thio Acids with Azides: A New Mechanism and New Synthetic Applications

2. A convenient and highly chemoselective method for the reductive acetylation of azides

3. A simple synthesis of 2,2-disubstituted tetrahydrothiophenes

4. Highly Efficient Coupling of β-Substituted Aminoethane Sulfonyl Azides with Thio Acids, toward a New Chemical Ligation Reaction

5. Synthesis of histone H3 proteins by a thioacid capture ligation strategy

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