Vicarious nucleophilic substitution of hydrogen in nitroarenes with in situ generated carbanions of 1-methyl-3-chloro-1,3-dihydro-2,1-benzisothiazole 2,2-dioxides

Synthesis

Volumn , Issue 10, 2003, Pages 1503-1505

  Wojciechowski, Krzysztof ^a   Modrzejewska, Helena ^a  

^a INSTITUTE OF ORGANIC CHEMISTRY   (Poland)

Author keywords

Benzosultams; Carbanions; Halogenation; Nitro compounds; Nucleophilic aromatic substitution

Indexed keywords

ALKALINITY; BENZENE; DERIVATIVES; MIXTURES; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

EQUIMOLAR MIXTURES;

NITROGEN COMPOUNDS;

1 METHYL 3 CHLORO 1,3 DIHYDRO 2,1 BENZISOTHIAZOLE 2,2 DIOXIDE DERIVATIVE; 1,3 DIHYDRO 2,1 BENZISOTHIAZOLE 2,2 DIOXIDE; 3 CHLORO 1,3 DIHYDRO 2,1 BENZISOTHIAZOLE 2,2 DIOXIDE; AROMATIC NITRO COMPOUND; HYDROGEN; UNCLASSIFIED DRUG;

ARTICLE; ARYLATION; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; STRUCTURE ANALYSIS; SUBSTITUTION REACTION; SYNTHESIS;

EID: 0042745383     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-40530     Document Type: Article

References (13)

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