J. Hirschler et al., A DIMERIC (PHENYLSULFONYL)OXAZOLIDINE, Acta crystallographica. Section C, Crystal structure communications, 50, 1994, pp. 1279-1281
We report the crystal structure of ,3-oxazolidin-2-yl]-5-{2-(1R,2S)-[(
2R,4R,5R)-3-(p- idin-2-yl]-1-hydroxycyclopentyl}-1-cyclopentanone, C42
H44Cl2N2O(8)S(2) (1). The chlorophenyl-sulfonyl substituent is cis to
the phenyl ring on each oxazolidine heterocycle. Each chlorophenyl-sul
fonyl substituent adopts a folded conformation by which the aromatic r
ing shields the heterocycle. The oxazolidine rings have envelope confo
rmations with C(3) and O(17) out of their respective planes. An intra-
molecular exists between the hydroxyl group O(11) and the ketone O(7)
[O(11)...O(7) 2.840 Angstrom, O(11)-H(11)...O(7) 134.0 degrees].