Base-controlled selectivity in the synthesis of linear and angular fused quinazolinones by a palladium-catalyzed carbonylation/nucleophilic aromatic substitution sequence

Angewandte Chemie - International Edition

Volumn 53, Issue 29, 2014, Pages 7579-7583

  Chen, Jianbin ^a   Natte, Kishore ^a   Spannenberg, Anke ^a   Neumann, Helfried ^a   Langer, Peter ^a   Beller, Matthias ^a   Wu, Xiao Feng ^a  

^a UNIVERSITY OF ROSTOCK   (Germany)

Author keywords

carbonylation; domino reactions; nucleophilic aromatic substitution; palladium catalysts; quinazolinones

Indexed keywords

AROMATIC COMPOUNDS; CARBONYLATION; CATALYSIS; ISOMERS; REACTION KINETICS; SCAFFOLDS;

AROMATIC SUBSTITUTIONS; DOMINO REACTIONS; FACILE SYNTHESIS; NEW APPROACHES; NUCLEOPHILIC AROMATIC SUBSTITUTION; PALLADIUM CATALYST; PALLADIUM-CATALYZED; QUINAZOLINONES;

AROMATIZATION;

PALLADIUM; QUINAZOLINONE DERIVATIVE;

CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; ISOMERISM; X RAY CRYSTALLOGRAPHY;

CATALYSIS; CRYSTALLOGRAPHY, X-RAY; ISOMERISM; MODELS, MOLECULAR; PALLADIUM; QUINAZOLINONES;

EID: 84904515536     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201402779     Document Type: Article

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