Silver triflate catalyzed reaction of 2-alkynylbenzaldoxime with phenol: A general and facile route to 1-aroxyisoquinolines

Synthesis

Volumn , Issue 17, 2011, Pages 2810-2816

  Zheng, Danqing ^a   Wang, Zhiyong ^b   Wu, Jie ^a,c  

^a FUDAN UNIVERSITY   (China)

^b CHONGQING UNIVERSITY   (China)

^c SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

cyclizations; isoquinoline; phenol; phosphorus ligands; silver triflate

Indexed keywords

CATALYZED REACTIONS; CYCLIZATIONS; HEXAFLUOROPHOSPHATES; ISOQUINOLINES; PHOSPHORUS LIGANDS; TRIFLATES;

CATALYSIS; PHENOLS; PHOSPHORUS;

SILVER;

1 (4 CHLOROPHENOXY) 3 CYCLOPROPYLISOQUINOLINE; 1 (4 TERT BUTYLPHENOXY) 3 CYCLOPROPYL 6 FLUOROISOQUINOLINE; 1 (4 TERT BUTYLPHENOXY) 3 CYCLOPROPYL 6,7 DIMETHOXYISOQUINOLINE; 1 (4 TERT BUTYLPHENOXY) 3 CYCLOPROPYLISOQUINOLINE; 1 (4 TERT BUTYLPHENOXY) 3 PARA TOLYLISOQUINOLINE; 1 (4 TERT BUTYLPHENOXY) 3 PHENYLISOQUINOLINE; 1 (4 TERT BUTYLPHENOXY) 6 CHLORO 3 PHENYLISOQUINOLINE; 1 (4 TERT BUTYLPHENOXY) 6 FLUORO 3 PARA TOLYLISOQUINOLINE; 1 (4 TERT BUTYLPHENOXY) 6 FLUORO 3 PHENYLISOQUINOLINE; 1 (4 TERT BUTYLPHENOXY) 6 METHOXY 3 PHENYLISOQUINOLINE; 1 (4 TERT BUTYLPHENOXY) 6,7 DIMETHOXY 3 PHENYLISOQUINOLINE; 1 (4 TERT BUTYLPHENOXY) 7 METHYL 3 PHENYLISOQUINOLINE; 1 AROXYISOQUINOLINE DERIVATIVE; 1 PHENOXY 3 PHENYLISOQUINOLINE; 2 ALKYNYLBENZALDOXIME; 3 BUTYL 1 (4 TERT BUTYLPHENOXY)ISOQUINOLINE; 3 CYCLOPROPYL 1 (2,6 DIMETHYLPHENOXY)ISOQUINOLINE; 3 CYCLOPROPYL 1 (4 METHOXYPHENOXY)ISOQUINOLINE; 3 CYCLOPROPYL 1 PHENOXYISOQUINOLINE; 3 CYCLOPROPYL 6 FLUORO 1 PHENOXYISOQUINOLINE; 3 CYCLOPROPYL 6,7 DIMETHOXY 1 PHENOXYISOQUINOLINE; 6 FLUORO 1 PHENOXY 3 PHENYLISOQUINOLINE; 6 METHOXY 1 PHENOXY 3 PHENYLISOQUINOLINE; 6,7 DIMETHOXY 1 PHENOXY 2 PHENYLISOQUINOLINE; ETHYL 4 (3 CYCLOPROPYLISOQUINOLIN 1 YLOXY)BENZOATE; ISOQUINOLINE DERIVATIVE; PHENOL; SILVER DERIVATIVE; TRIFLUOROMETHANESULFONIC ACID; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE;

EID: 80052055155     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1260121     Document Type: Article

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