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Concise synthesis of Didebromohamacanthin A and Demethylaplysinopsine: Addition of Ethylenediamine and Guanidine Derivatives to the Pyrrole-Amino Acid Diketopiperazines in Oxidative Conditions
- Source :
- Organic Letters, Organic Letters, American Chemical Society, 2014, 16 (3), pp.872-5. ⟨10.1021/ol4036177⟩
- Publication Year :
- 2014
- Publisher :
- American Chemical Society (ACS), 2014.
-
Abstract
- International audience; Oxidative nucleophilic addition of ethylenediamine and guanidine derivatives to pyrrole-amino acid diketopiperazines was shown to provide substituted 5,6-dihydro-2(1H)-piperazinones, quinoxalinones, and 2-aminoimidazolones. On the basis of this methodology, a concise approach to natural products didebromohamacanthin A and demethylaplysinopsine has been demonstrated.
- Subjects :
- Ethylenediamine
Stereoisomerism
Diketopiperazines
Oxidative phosphorylation
010402 general chemistry
01 natural sciences
Biochemistry
Indole Alkaloids
chemistry.chemical_compound
Molecule
Organic chemistry
Pyrroles
Amino Acids
Physical and Theoretical Chemistry
Guanidine
Pyrrole
chemistry.chemical_classification
Nucleophilic addition
Molecular Structure
[CHIM.ORGA]Chemical Sciences/Organic chemistry
010405 organic chemistry
Chemistry
Organic Chemistry
Ethylenediamines
0104 chemical sciences
Amino acid
Oxidation-Reduction
Subjects
Details
- ISSN :
- 15237052 and 15237060
- Volume :
- 16
- Database :
- OpenAIRE
- Journal :
- Organic Letters
- Accession number :
- edsair.doi.dedup.....00f2136003f0bad96e3a528bdd885891