Superacid-promoted reactions of N-acyliminium ions: An effective route to substituted 3-oxo-1,2,3,4-tetrahydroisoquinolines and related products

Synthesis

Volumn , Issue 11, 2006, Pages 1775-1780

  Zhang, Yiliang ^a   Kindelin, Patrick J ^a   DeSchepper, Daniel J ^a   Zheng, Chong ^a   Klumpp, Douglas A ^a  

^a NORTHERN ILLINOIS UNIVERSITY   (United States)

Author keywords

Electrophilic aromatic substitutions; N acyliminium ions; Superacid; Superelectrophile; Tetrahydroisoquinolines

Indexed keywords

CHEMICAL REACTIONS; ESTERS; IONS; MOLECULAR DYNAMICS; ORGANIC ACIDS;

ELECTROPHILIC AROMATIC SUBSTITUTIONS; N-ACYLIMINIUM IONS; SUPERACID; SUPERELECTROPHILE; TETRAHYDROISOQUINOLINES;

REACTION KINETICS;

1 (4 FLUROPHENYL) 2 PHENYL 1,2,3,4 TETRAHYDOISOQUINOLINE; 1 PENTAFLUOROPHENYL 2 PHENYL 1,2,3,4 TETRAHYDROISOQUINOLINE; 5,8 DIMETHOXY 1,2 DIPHENYL 1,2,3,4 TETRAHYDROISOQUINOLINE; 7 FLUORO 1,2 DIPHENYL 1,2,3,4 TETRAHYDROISOQUINOLINE; ISOQUINOLINE DERIVATIVE; TRIFLUOROMETHANESULFONIC ACID; UNCLASSIFIED DRUG;

ARTICLE; CHIRALITY; CYCLIZATION; STEREOCHEMISTRY;

EID: 33745121878     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-942387     Document Type: Article

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