Total synthesis of the proposed structure of talarolide A-Reference-Cited by-同舟云学术

Total synthesis of the proposed structure of talarolide A

Published:2018 Issue:29 Volume:16 Page:5286-5293
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Zhang Shengping¹²³⁴,De Leon Rodriguez Luis M.⁵²³⁴^ORCID,Huang Renjie¹²³⁴,Leung Ivanhoe K. H.¹²³⁴^ORCID,Harris Paul W. R.¹²³⁴⁵^ORCID,Brimble Margaret A.¹²³⁴⁵^ORCID

Affiliation:

1. School of Chemical Sciences

2. The University of Auckland

3. Auckland

4. New Zealand

5. Maurice Wilkins Centre for Molecular Biodiscovery

Abstract

The proposed structure of talarolide A, a cycloheptapeptide featuring a hydroxamate moiety within the peptide backbone, was successfully synthesized.

Funder

China Scholarship Council

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB01230J

Reference31 articles.

1. Peptide siderophores

2. Pargamicin A, a Novel Cyclic Peptide Antibiotic from Amycolatopsis sp.

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4. Biological activities of pargamicin A, a novel cyclic peptide antibiotic from Amycolatopsis sp.

5. Polyoxypeptin isolated from Streptomyces: A bioactive cyclic depsipeptide containing the novel amino acid 3-hydroxy-3-methylproline

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