Synthesis of fully protected (2 R ,3 R ,4 S )-4-amino-7-guanidino-2,3-dihydroxy heptanoic acid
Author:
Funder
Japan Society for the Promotion of Science
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference29 articles.
1. Callipeltin A, an Anti-HIV Cyclic Depsipeptide from the New Caledonian Lithistida Sponge Callipelta sp.
2. Neamphamide A, a New HIV-Inhibitory Depsipeptide from the Papua New Guinea Marine Sponge Neamphius huxleyi
3. New cytotoxic callipeltins from the Solomon Island marine sponge Asteropus sp.
4. 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
5. Preparation of (2 R , 3 R , 4 R )-3-hydroxy-2,4,6-trimethylheptanoic acid via enzymatic desymmertization
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1. Stereoselective Synthesis of a Protected Side Chain of Callipeltin A;Organic Letters;2022-09-23
2. Synthesis of the cyclic heptapeptide core of callipeltin A;Organic Chemistry Frontiers;2022
3. Cyclic Depsipeptides, Callipeltins;Topics in Heterocyclic Chemistry;2020
4. Asymmetric synthesis of (2S,3S)-3-Me-glutamine and (R)-allo-threonine derivatives proper for solid-phase peptide coupling;Amino Acids;2018-11-17
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