The cobalt way to angucyclinones: Asymmetric total synthesis of the antibiotics (+)-rubiginone B2, (-)-tetrangomycin, and ( - ) -8- O-Methyltetrangomycin

Chemistry - A European Journal

Volumn 16, Issue 29, 2010, Pages 8805-8821

  Kesenheimer, Christian ^a   Kalogerakis, Aris ^a   Meißner, Anja ^a   Groth, Ulrich ^a  

^a UNIVERSITY OF KONSTANZ   (Germany)

Author keywords

Angucyclinone; Catalysis; Cobalt; Cycloaddition; Natural products

Indexed keywords

3-HYDROXYBENZOIC ACIDS; [2+2+2] CYCLOADDITION; ANGUCYCLINONE; ASYMMETRIC TOTAL SYNTHESIS; CYCLOPENTADIENYLS; DEPROTECTION; NATURAL PRODUCTS; NATURALLY OCCURRING; STARTING MATERIALS;

ACIDS; CATALYSIS;

COBALT;

3,4 DIHYDRO 3 HYDROXY 8 METHOXY 3 METHYL 2H BENZ[A]ANTHRACENE 1,7,12 TRIONE; ANGUCYCLINONE; ANTHRAQUINONE DERIVATIVE; ANTIINFECTIVE AGENT; BENZ[A]ANTHRACENE DERIVATIVE; COBALT; RUBIGINONE B2; TETRANGOMYCIN;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; SYNTHESIS;

ANTHRAQUINONES; ANTI-BACTERIAL AGENTS; BENZ(A)ANTHRACENES; COBALT; MOLECULAR STRUCTURE;

EID: 77955135503     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201000804     Document Type: Article

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