Chiron approach to callipeltin A: first synthesis of fully protected (2R,3R,4S)-4,7-diamino-2,3-dihydroxy heptanoic acid
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference8 articles.
1. Bioorganic Marine Chemistry;Ireland,1989
2. Callipeltin A, an Anti-HIV Cyclic Depsipeptide from the New Caledonian Lithistida Sponge Callipelta sp.
3. Callipeltins B and C; bioactive peptides from a marine Lithistida sponge Callipelta sp
4. A Facile Synthetic Route to a Third-Generation Dendrimer with Generation-Specific Functional Aryl Bromides
5. The Reaction of Free Carbonyl Sugar Derivatives with Organometallic Reagents. I. 6-Deoxy-L-idose and Derivatives1,2
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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. Synthesis of fully protected (2 R ,3 R ,4 S )-4-amino-7-guanidino-2,3-dihydroxy heptanoic acid;Tetrahedron Letters;2017-04
4. Conformation and NH stretching of 1,1-dihalogenoheptan-1-amines [CH3(CH2)5CX2NH2; X=F, Cl or Br]: Halogen and solvent effects;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;2015-03
5. Vibrational spectroscopic investigation and conformational analysis of 1-heptylamine: A comparative density functional study;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;2013-10
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