K. Park et al., HYLENEDIOXY)-1,5-DIMETHYLBICYCLO[4.4.0]DECAN-4-ONE, Acta crystallographica. Section C, Crystal structure communications, 51, 1995, pp. 268-270
The title compound (1) [alternative name: ydronaphthalene)-1-spiro-2'-
(1',3'-dioxolan)-6one, C14H22O3] was obtained as the major product upo
n Pd/CaCO3-catalyzed hydrogenation of the corresponding enone (2). The
analysis of the crystal structure of (1) has established that the mon
oacetal is cis-fused and that both rings adopt nearly perfect chair fo
rms. The C(5) methyl group is in an alpha position, resulting directly
from syn-hydrogenation of the enone. While there are two possible cha
ir-chair conformations for cis-decalins, the title compound crystalliz
ed in the conformation which places the C(5) methyl group in an equato
rial position.