Quinone Imides. XXIII. Addition Reactions of p-Quinonedibenzimide and Related Compounds

1952 ◽  
Vol 74 (23) ◽  
pp. 5872-5876 ◽  
Author(s):  
Roger Adams ◽  
D. S. Acker
1979 ◽  
Vol 32 (2) ◽  
pp. 353 ◽  
Author(s):  
RAJ Smith ◽  
AR Lal

The syntheses of potential α-sulfur-substituted carbanion precursors (2a-h) are reported and the results of their subsequent reactions with strong bases are presented. The relatively stable carbanions (3a-d) were made to react with a variety of α,β-unsaturated ketones and the yields of 1,4 and 1,2 addition products were determined.


1970 ◽  
Vol 48 (10) ◽  
pp. 1566-1573 ◽  
Author(s):  
J. Bryan Jones ◽  
John M. Young

Studies on the reactions of carcinogenic γ-lactones and related compounds with analogues of guanine DNA residues indicate that the lactones themselves will not effect permanent alkylation of the guanine N-7 position since the Michael addition reactions involved would be readily reversible. In contrast, the α,β-unsaturated acids resulting from hydrolysis of such lactones are effective guanine N-7 alkylating agents owing to zwitterionic stabilization of the corresponding Michael addition products.


Heterocycles ◽  
1975 ◽  
Vol 3 (12) ◽  
pp. 1113 ◽  
Author(s):  
Hiroshi Yamanaka ◽  
Takayuki Shiraishi ◽  
Takao Sakamoto

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