Regiospecificity in the reaction of 2,3-dichloronaphthazarins with azide anions. Synthesis of echinamine A - A metabolite produced by the sea urchin Scaphechinus mirabilis

Tetrahedron Letters

Volumn 47, Issue 9, 2006, Pages 1385-1387

  Pokhilo, Nataly D ^a   Yakubovskaya, Alla Ya ^a   Denisenko, Vladimir A ^a   Anufriev, Victor Ph ^a  

^a PACIFIC INSTITUTE OF BIOORGANIC CHEMISTRY   (Russian Federation)

Author keywords

2,3 Dichloronaphthazarins; 3 Amino 7 ethyl 2,5,6,8 tetrahydroxy 1,4 naphthoquinone; Azido group; Echinamine A; Regiospecificity of substitution; Sea urchin, Scaphechinus mirabilis (Agassiz)

Indexed keywords

3 AMINO 7 ETHYL 2,5,6,8 TETRAHYDROXY 1,4 NAPHTHOQUINONE; 6 ALKOXY 2,3 DICHLORONAPHTHAZARIN DERIVATIVE; 6 HYDROXY 2,3 DICHLORONAPHTHAZARIN DERIVATIVE; AZIDE; METHANOL; NAPHTHAZARIN; QUINONE DERIVATIVE; SODIUM AZIDE; UNCLASSIFIED DRUG;

ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; METABOLITE; SEA URCHIN;

ECHINOIDEA; SCAPHECHINUS MIRABILIS;

EID: 31444456552     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.12.109     Document Type: Article

References (18)

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