Rediscovery, Isolation, and Asymmetric Reduction of 1,2,3,4‐Tetrahydronaphthalene‐1,4‐dione and Studies of Its [Cr(CO)₃] Complex

Abstract

For 25 years it has been known that 1,4-dihydroxynaphthalene and tetrahydronaphthalene-1,4-dione coexist as stable tautomers; however, the dione has now emerged as an interesting starting material for synthesis. Its efficient isolation is reported, and the corresponding [Cr(CO)3] complexes of the two tautomers are prepared, thus leading to efficient desymmetrization using chiral diamine acyl-transfer catalysts (see scheme).