10b-Substituted hexahydropyrrolo-isoquinolines: Studies on diastereoselective formation of a quaternary carbon stereocenter via N-acyliminium ion cyclization

Tetrahedron

Volumn 62, Issue 5, 2006, Pages 943-953

  Kałuza, Zbigniew ^a   Mostowicz, Danuta ^a   Dołȩga, Grzegorz ^a   Mroczko, Katarzyna ^a   Wójcik, Robert ^a  

^a INSTITUTE OF ORGANIC CHEMISTRY   (Poland)

Author keywords

Diastereoselective synthesis; Isoquinoline alkaloids; N Acyliminium ion cyclization

Indexed keywords

ACID; CARBON; CARBONYL DERIVATIVE; CATION; IMIDE; ISOQUINOLINE DERIVATIVE; LEWIS ACID; N ACYLIMINIUM; SOLVENT; TARTARIC ACID; UNCLASSIFIED DRUG;

ACETYLATION; ARTICLE; CATALYSIS; CHEMICAL BOND; CONCENTRATION (PARAMETERS); CYCLIZATION; GRIGNARD REACTION; METHODOLOGY; PRIORITY JOURNAL; STEREOCHEMISTRY; SYNTHESIS; TEMPERATURE;

EID: 29244442603     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.10.028     Document Type: Article

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