Divergent reaction pathways of homologous and isosteric propargyl amides in sequential Ru/Pd-catalyzed annulations for the synthesis of heterocycles

Journal of Organic Chemistry

Volumn 78, Issue 8, 2013, Pages 3832-3846

  Raikar, Sandeep N ^a   Malinakova, Helena C ^a  

^a UNIVERSITY OF KANSAS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BENZOYL CHLORIDES; CYCLIZATION PATHWAYS; HECK CYCLIZATION; REACTION PATHWAYS; RING CLOSING METATHESIS; SEQUENTIAL ADDITION; SYNTHETIC EFFICIENCY; THREE-COMPONENT COUPLING;

CATALYSIS; CHLORINE COMPOUNDS;

CYCLIZATION;

ALKYNE DERIVATIVE; AMIDE; CHLORINE DERIVATIVE; CYCLOPROPANE DERIVATIVE; IMINE; LEAD; PHENANTHROLINE DERIVATIVE; PYRIDINE DERIVATIVE; QUINOLINE DERIVATIVE; RUTHENIUM;

ANNULATION REACTION; ARTICLE; CATALYSIS; CATALYST; CYCLIZATION; HECK REACTION; ONE POT SYNTHESIS; RING CLOSING METATHESIS; SYNTHESIS;

AMIDES; CATALYSIS; HETEROCYCLIC COMPOUNDS; MOLECULAR STRUCTURE; PALLADIUM; PARGYLINE; RUTHENIUM; STEREOISOMERISM;

EID: 84876592043     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo400246d     Document Type: Article

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