Solution-Phase Peptide Synthesis; Synthesis of 'North-Western' and 'South-Eastern' Fragments of the Antifungal Cyclodepsipeptide Petriellin A-Reference-Cited by-同舟云学术

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Solution-Phase Peptide Synthesis; Synthesis of 'North-Western' and 'South-Eastern' Fragments of the Antifungal Cyclodepsipeptide Petriellin A

Published:2008 Issue:8 Volume:61 Page:615
ISSN:0004-9425
Container-title:Australian Journal of Chemistry
language:en
Short-container-title:Aust. J. Chem.

Author:

Aurelio Luigi,Brownlee Robert T. C.,Hughes Andrew B.

Abstract

The solution-phase synthesis of two highly modified peptides, a hexamer and a heptamer, that constitute the two halves of the antifungal cyclic depsipeptide, Petriellin A, is reported.

Publisher

CSIRO Publishing

Subject

General Chemistry

Link

http://www.publish.csiro.au/CH/pdf/CH08132

Reference19 articles.

1. The Facile Production of N-Methyl Amino Acids via Oxazolidinones

2. A Novel Synthesis of N-Methyl Asparagine, Arginine, Histidine, and Tryptophan

3. An Efficient Synthesis of N-Methyl Amino Acids by Way of Intermediate 5-Oxazolidinones

4. Synthetic Preparation of N-Methyl-α-amino Acids

5. Synthesis and Structural Characterization of N-Methyl-DL-glutamic Acid

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1. Effective Synthesis and Antifouling Activity of Dolastatin 16 Derivatives;Marine Drugs;2022-02-04

2. Macrocyclic N-Methylated Cyclic Peptides and Depsipeptides;Studies in Natural Products Chemistry;2015

3. First total synthesis of prunustatin A;Tetrahedron Letters;2014-02

4. Total Synthesis of the Antifungal Depsipeptide Petriellin A;The Journal of Organic Chemistry;2011-07-19

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