Gold(I)-catalyzed 1,2-acyloxy migration/[3+2] cycloaddition of 1,6-diynes with an ynamide propargyl ester moiety: Highly efficient synthesis of functionalized cyclopenta[b]indoles

Chemistry - A European Journal

Volumn 21, Issue 3, 2015, Pages 1009-1013

  Liu, Jun ^a   Chen, Ming ^a   Zhang, Liangwei ^a,b   Liu, Yuanhong ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

^b CHINA PHARMACEUTICAL UNIVERSITY   (China)

Author keywords

Cycloaddition; Gold; Homogeneous catalysis; Propargyl ester; Ynamides

Indexed keywords

CATALYSIS; CYCLOADDITION; ESTERIFICATION; ESTERS; ISOMERIZATION; REACTION INTERMEDIATES; REACTION KINETICS; SYNTHESIS (CHEMICAL);

CYCLOISOMERIZATIONS; DOUBLE-BOND ISOMERIZATION; EFFICIENT SYNTHESIS; HOMOGENEOUS CATALYSIS; MECHANISTIC STUDIES; PROPARGYL ESTERS; YNAMIDES; [3+2]-CYCLOADDITION;

GOLD;

ALKYNE DERIVATIVE; AMIDE; COORDINATION COMPOUND; CYCLOPENTANE DERIVATIVE; ESTER; GOLD; INDOLE; INDOLE DERIVATIVE;

CATALYSIS; CHEMISTRY; CYCLOADDITION; ISOMERISM;

AMIDES; CATALYSIS; COORDINATION COMPLEXES; CYCLOADDITION REACTION; CYCLOPENTANES; DIYNES; ESTERS; GOLD; INDOLES; ISOMERISM;

EID: 84920800099     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201405965     Document Type: Article

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