Investigations of the key macrolactamisation step in the synthesis of cyclic tetrapeptide pseudoxylallemycin A
Author:
Affiliation:
1. School of Chemical Sciences
2. The University of Auckland
3. Auckland 1010
4. New Zealand
5. The Maurice Wilkins Centre for Molecular Biodiscovery
6. School of Biological Sciences
Abstract
During total synthesis of pseudoxylallemycin A, an unstable intermediate was observed and appeared to be reactivated by coupling reagent by-products.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB00227H
Reference47 articles.
1. Pseudoxylallemycins A–F, Cyclic Tetrapeptides with Rare Allenyl Modifications Isolated from Pseudoxylaria sp. X802: A Competitor of Fungus-Growing Termite Cultivars
2. Cyclic tetrapeptides from marine bacteria associated with the seaweed Diginea sp. and the sponge Halisarca ectofibrosa
3. Isolation and Structural Elucidation of Cyclic Tetrapeptides from Onychocola sclerotica
4. Nouveaux cyclotétrapeptides isolés de l'ascidie cystodytes delle chiajei.
5. Two new cyclic tetrapeptides from deep-sea bacterium Bacillus amyloliquefaciens GAS 00152
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