Corrigendum to "Lewis acid catalyzed intramolecular halo-arylation of tethered alkenes using N-halosuccinimide (NXS) as the halogen source: a general method for the synthesis of chromanones, chromans, quinolones, tetrahydroquinolines and tetralins". [Tetrahedron Lett. 46 (2005) 8599] (DOI:10.1016/j.tetlet.2005.09.170);Lewis acid catalyzed intramolecular halo-arylation of tethered alkenes using N-halosuccinimide (NXS) as the halogen source: A general method for the synthesis of chromanones, chromans, quinolones, tetrahydroquinolines and tetralins

Tetrahedron Letters

Volumn 46, Issue 49, 2005, Pages 8599-8603

  Hajra, Saumen ^a   Maji, Biswajit ^a   Karmakar, Ananta ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY   (India)

Author keywords

Catalyst; Chromanones; Chromans; Halo arylation; Lewis acid; N Halosuccinimide; Quinolones; Tetrahydroquinolines; Tetralins

Indexed keywords

4 CHROMANONE DERIVATIVE; ALKENE DERIVATIVE; CHROMAN DERIVATIVE; HALOGEN; LEWIS ACID; QUINOLINE DERIVATIVE; QUINOLONE DERIVATIVE; SUCCINIMIDE DERIVATIVE; TETRALIN DERIVATIVE;

ARTICLE; ARYLATION; CATALYSIS; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; MOLECULAR INTERACTION; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 27644535373     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.10.152     Document Type: Erratum

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53. 8a) was found.