Efficient formation of σH-adducts as a key step in the synthesis of acridines via Lewis acid-promoted transformations of the nitro group

Tetrahedron

Volumn 63, Issue 45, 2007, Pages 11048-11054

  Bobin, Mariusz ^a   Kwast, Andrzej ^b   Wróbel, Zbigniew ^b  

^a WARSAW UNIVERSITY OF TECHNOLOGY   (Poland)

^b INSTITUTE OF ORGANIC CHEMISTRY   (Poland)

Author keywords

Carbanions; Cyclisation; Heterocycles; Nitroarenes; Nitroso group

Indexed keywords

ACRIDINE; ACRIDINE DERIVATIVE; AROMATIC NITRO COMPOUND; BENZYL CYANIDE DERIVATIVE; HETEROCYCLIC COMPOUND; LEWIS ACID; NITRO DERIVATIVE;

ACYLATION; ARTICLE; CHEMICAL REACTION KINETICS; METHODOLOGY; ONE POT SYNTHESIS; PRIORITY JOURNAL; REDUCTION; SILYLATION; SUBSTITUTION REACTION; SYNTHESIS;

EID: 34648820638     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.08.042     Document Type: Article

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