Total synthesis of the biscarbazole alkaloids murrafolinea a-d by a domino sonogashira coupling/claisen rearrangement/electrocyclization reaction

Angewandte Chemie - International Edition

Volumn 52, Issue 42, 2013, Pages 11073-11077

  Kumar, V Pavan ^a   Gruner, Konstanze K ^a   Kataeva, Olga ^a   Knölker, Hans Joachim ^a  

^a DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

Author keywords

alkaloids; C H bond activation; natural products; palladium; X ray diffraction

Indexed keywords

CH-BOND ACTIVATION; CLAISEN REARRANGEMENT; DOMINO REACTIONS; ELECTROCYCLIZATION; NATURAL PRODUCTS; ONE-POT PROCEDURES; SONOGASHIRA COUPLING; TOTAL SYNTHESIS;

ALKALOIDS; METABOLITES; PALLADIUM; REACTION KINETICS; X RAY DIFFRACTION;

NITROGEN COMPOUNDS;

ALKALOID; CARBAZOLE DERIVATIVE; PALLADIUM;

ARTICLE; C H BOND ACTIVATION; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; CYCLIZATION; NATURAL PRODUCTS; STEREOISOMERISM; SYNTHESIS; X RAY CRYSTALLOGRAPHY; X RAY DIFFRACTION;

ALKALOIDS; C H BOND ACTIVATION; NATURAL PRODUCTS; PALLADIUM; X-RAY DIFFRACTION;

ALKALOIDS; CARBAZOLES; CATALYSIS; CRYSTALLOGRAPHY, X-RAY; CYCLIZATION; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 84885448907     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201305993     Document Type: Article

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52. 3 per cell unit), which were modeled by dichloromethane and water molecules. CCDCa 948511 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.