ChemInform Abstract: Reactions of Organic Anions. Part 138. Vicarious Nucleophilic Substitution of Hydrogen versus Bis-Annulation in the Reaction of Chloromethyl Aryl Sulfone Carbanion with Electrophilic Arenes.

ChemInform ◽  
1987 ◽  
Vol 18 (37) ◽  
Author(s):  
M. MAKOSZA ◽  
T. GLINKA ◽  
S. OSTROWSKI ◽  
A. RYKOWSKI
1990 ◽  
Vol 68 (12) ◽  
pp. 2239-2241 ◽  
Author(s):  
Stanisław Ostrowski ◽  
Krzysztof Wojciechowski

The Vicarious Nucleophilic Substitution of hydrogen in 4-nitrobenzofuroxan derivatives by carbanions of chloromethyl phenyl sulfone, chloromethyl p-tolyl sulfone, chloromethyl tert-butyl sulfone, and N,N-dimethyl chloromethane sulfonamide proceeds at positions 5 and 7. In some cases the Boulton–Katritzky rearrangement of the products obtained, leading to more stable 7-substituted isomers, was observed. Keywords: carbanions, nitrobenzofuroxans, sulfones, Vicarious Nucleophilic Substitution, Boulton–Katritzky rearrangement.


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