Issue 8, 1969

Metal hydride reductions of endo-tricyclo[5,2,1,02,6]deca-4,8-dien-3-one (endo-dicyclopentadienone)

Abstract

Aluminium hydride, lithium tri-t-butoxy-aluminium hydride, and sodium borohydride reduce specifically the carbonyl group, the double bond, and both the carbonyl group and the double bond, respectively, of a conjugated cyclopentenone, while lithium aluminium hydride gives all three products in varying amounts depending on the reaction conditions.

Article information

Article type
Paper

J. Chem. Soc. D, 1969, 417-417

Metal hydride reductions of endo-tricyclo[5,2,1,02,6]deca-4,8-dien-3-one (endo-dicyclopentadienone)

W. L. Dilling and R. A. Plepys, J. Chem. Soc. D, 1969, 417 DOI: 10.1039/C29690000417

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