DESIGN, SYNTHESIS, AND STUDY OF SIMPLE MONOCYCLIC CONJUGATED ENEDIYNES - THE 10-MEMBERED RING ENEDIYNE MOIETY OF THE ENEDIYNE ANTICANCER ANTIBIOTICS

Following the discovery of the enediyne anticancer antibiotics, investigations were initiated directed toward the design, synthesis, and study of simple monocyclic conjugated enediynes. In this article the synthesis of the parent 10-membered ring enediyne found in the enediyne natural products and its properties are described. In addition to the parent hydrocarbon 27, the synthetic methodology developed based on the Ramberg-Backlund reaction delivers a series of higher ring homologs (17-22) and the water soluble version of the 10-membered ring compound 47. Molecular mechanics calculations on these systems led to a number of geometrical parameters which correlated well with their tendencies to undergo the Bergman cycloaromatization reaction. Kinetic studies on the Bergman cycloaromatization of the 10-membered ring enediynes 27 and 47 led to the following thermodynamic values: 27, energy of activation (E(a)) = 23.8 kcal/mol, DELTA-G double dagger (37-degrees-C) = 24.6 kcal/mol; 47, energy of activation (E(a)) = 31.5 kcal/mol, DELTA-G double dagger (37-degrees-C) = 24.8 kcal/mol. The designed enediyne 47 showed potent DNA-cleaving properties becoming the first synthetic molecule to mimic the action of the naturally occurring enediynes in this regard.