Synthesis of the cyclic heptapeptide core of callipeltin A
Author:
Affiliation:
1. Institute of Organic Chemistry, Saarland University, P.O. Box 151150, 66041 Saarbrücken, Germany
Abstract
Funder
Universität des Saarlandes
Deutsche Forschungsgemeinschaft
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2022/QO/D2QO01120D
Reference59 articles.
1. Callipeltin A, an Anti-HIV Cyclic Depsipeptide from the New Caledonian Lithistida Sponge Callipelta sp.
2. Isolation of callipeltins A–C and of two new open-chain derivatives of callipeltin A from the marine sponge Latrunculia sp. A revision of the stereostructure of callipeltins
3. Concise Synthesis of All Stereoisomers of β-Methoxytyrosine and Determination of the Absolute Configuration of the Residue in Callipeltin A
4. Quantum Mechanical Calculation of Coupling Constants in the Configurational Analysis of Flexible Systems: Determination of the Configuration of Callipeltin A
5. Callipeltins B and C; bioactive peptides from a marine Lithistida sponge Callipelta sp
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