Issue 21, 1989

Diversity of the C–C bond formation in the reaction of a 5-bromouracil derivative with carbanions

Abstract

The reaction of 5-bromo-1,3-dimethyluracil (1) with active methylene compounds in the presence of base gave 5,6-disubstituted 5,6-dihydrouracil derivative (2), 2,4-diazabicyclo[4.1.0]heptane derivatives (4), and 2,4-diazabicyclo[4.3.0]nonane derivative (5), the formation of which was significantly dependent on the nature of the carbaions.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 1659-1660

Diversity of the C–C bond formation in the reaction of a 5-bromouracil derivative with carbanions

K. Hirota, H. Sajiki, Y. Maki, H. Inoue and T. Ueda, J. Chem. Soc., Chem. Commun., 1989, 1659 DOI: 10.1039/C39890001659

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