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Novel reactions of 5-bromouracil derivatives with active methylene compounds
Nucleic Acids Symposium Series
|January 1, 1986
Abstract:
5-Bromouracil derivatives (1) reacted with carbanions at room temperature to give 6-substituted uracils (6), 2,4-diazabicyclo[4,1,0] heptanes (8) and 2,4-diazabicyclo[4,3,0]nonane derivative (9), which depend largely upon the structure of the active methylene compounds employed for the generation of carbanions.