Vicarious Nucleophilic Substitution of Hydrogen and Formation of Aziridine Rings in Reactions of Benzonaphthyridines and their N-Oxides with Chloromethyl Phenyl Sulfone

2001 ◽  
Vol 132 (7) ◽  
pp. 849-854 ◽  
Author(s):  
Barbara Bachowska ◽  
Teresa Zujewska
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.


ChemInform ◽  
2010 ◽  
Vol 28 (23) ◽  
pp. no-no
Author(s):  
M. D. DREW ◽  
D. A. JACKSON ◽  
N. J. LAWRENCE ◽  
J. LIDDLE ◽  
R. G. PRITCHARD

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