Divergent Synthesis of Aeruginosins Based on a C(sp3)£H Activation Strategy

Chemistry - A European Journal

Volumn 21, Issue 26, 2015, Pages 9370-9379

  Dailler, David ^a   Danoun, Grégory ^a   Ourri, Benjamin ^a   Baudoin, Olivier ^a  

^a UNIVERSITÉ LYON 1   (France)

Author keywords

aeruginosin; C H activation; marine natural products; palladium catalysis; total synthesis

Indexed keywords

AMINO ACIDS; CATALYSIS; HALOGENATION; MOLECULES; STEREOCHEMISTRY;

2-CARBOXY-6-HYDROXYOCTAHYDROINDOLE; AERUGINOSIN; DIVERGENT SYNTHESIS; FRAGMENT COUPLING; INHIBITORY ACTIVITY; MARINE NATURAL PRODUCTS; PALLADIUM CATALYSIS; TOTAL SYNTHESIS;

CHEMICAL ACTIVATION;

2-CARBOXY-6-HYDROXYOCTAHYDROINDOLE; AERUGINOCIN; AERUGINOSIN 298-A; BACTERIOCIN; BIOLOGICAL PRODUCT; INDOLE DERIVATIVE; LEUCINE; PALLADIUM; SERINE PROTEINASE;

ANALOGS AND DERIVATIVES; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

BACTERIOCINS; BIOLOGICAL PRODUCTS; CATALYSIS; INDOLES; LEUCINE; MOLECULAR STRUCTURE; PALLADIUM; SERINE PROTEASES; STEREOISOMERISM;

EID: 84934915463     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201501370     Document Type: Article

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