A novel one-pot, three-component access to hexahydropyrrolo[2,1-a] isoquinolines by an alkylation-dehydrohalogenation-1,3-dipolar cycloaddition sequence

Synthesis

Volumn , Issue 12, 2005, Pages 2039-2045

  Nyerges, Miklós ^a   Somfai, Barbara ^a   Tóth, Judit ^a   Toke, László ^a   Dancsó, András ^b   Blaskó, Gábor ^b  

^a BUDAPEST UNIVERSITY OF TECHNOLOGY AND ECONOMICS   (Hungary)

^b EGIS PHARMACEUTICALS LTD   (Hungary)

Author keywords

Cycloadditions; Electrocyclic reactions; Heterocycles; Tandem reactions; Ylides

Indexed keywords

ADDITION REACTIONS; COMPLEXATION; HALOGENATION; NITROGEN COMPOUNDS; SALTS;

CYCLOADDITIONS; ELECTROCYCLIC REACTIONS; HETEROCYCLES; TANDEM REACTIONS; YLIDES;

SYNTHESIS (CHEMICAL);

AZELASTINE; AZOMETHINE YLIDE; ISOQUINOLINE DERIVATIVE;

ALKYLATION; ARTICLE; CYCLIZATION; CYCLOADDITION; HALOGENATION; STEREOCHEMISTRY; SYNTHESIS;

EID: 23744482006     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-869908     Document Type: Article

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