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Communication | Special issue | Vol 18, No. 1, 1982, pp.145-148
Published online, 1st January, 1970
DOI: 10.3987/S(B)-1982-01-0145
Quinuclidin-4-yl Anion. Generation and Stability Comparison by Radical Anion Reduction

Shelton Bank* and William K. S. Cleveland

*Department of Chemistry, State University of New York at Albany, Albany, New york 12222, U.S.A.

Abstract

Radical anion reduction of 4-bromoquinuclidine and 1-bromobicyclo[2.2.2]octane leads to similar product distributions. The lone pair of electrons on the nitrogen atom in the heterocyclic compound do not affect the anion stability.