diazonamide-a and ferric-chloride

diazonamide-a has been researched along with ferric-chloride* in 1 studies

Other Studies

1 other study(ies) available for diazonamide-a and ferric-chloride

Article	Year
FeCl3-mediated Friedel-Crafts hydroarylation with electrophilic N-acetyl indoles for the synthesis of benzofuroindolines. Angewandte Chemie (International ed. in English), 2012, Dec-07, Volume: 51, Issue:50 IRONic electrophilic indoles! The C3-regioselective hydroarylation of N-acetyl indoles with aromatic nucleophiles mediated by FeCl(3) features a rare example of the electrophilic reactivity of the indole core in a Friedel-Crafts reaction. This indole umpolung allows us straightforward access to the tetracyclic benzofuroindoline motif found in the natural product diazonamide A, which is a potent antitumor agent. Topics: Antineoplastic Agents; Catalysis; Chlorides; Ferric Compounds; Heterocyclic Compounds, 4 or More Rings; Indoles; Oxazoles; Stereoisomerism	2012

Article

Year

FeCl3-mediated Friedel-Crafts hydroarylation with electrophilic N-acetyl indoles for the synthesis of benzofuroindolines.

Angewandte Chemie (International ed. in English), 2012, Dec-07, Volume: 51, Issue:50

IRONic electrophilic indoles! The C3-regioselective hydroarylation of N-acetyl indoles with aromatic nucleophiles mediated by FeCl(3) features a rare example of the electrophilic reactivity of the indole core in a Friedel-Crafts reaction. This indole umpolung allows us straightforward access to the tetracyclic benzofuroindoline motif found in the natural product diazonamide A, which is a potent antitumor agent.

Topics: Antineoplastic Agents; Catalysis; Chlorides; Ferric Compounds; Heterocyclic Compounds, 4 or More Rings; Indoles; Oxazoles; Stereoisomerism

2012