8, 55.8, 114.4, 122.6, 124.4, 125.8, 128.1, 128.2, 129.2, 132.0, 133.3, 142.8, 143.0, 165.2, 186.9; MS (CI): 483 (M + ). Synthesis of DCTE Compounds 7a±10a: A solution of aldehyde 3 or the appropriate ketone 4±6 (0.1 mmol) and malonodinitrile (16.5 mg, 0.25 mmol) in anhydrous dichloroethane (5 mL) was cooled in an ice bath to 0 C under nitrogen atmosphere and treated with TiCl 4 (0.1 mL, 0.91 mmol) dropwise. After stirring for 5 min, pyridine (0.2 mL) was carefully added over 20 min. The purple reaction mixture was allowed to warm to room temperature and subsequently heated at reflux for 5±10 min during which time a white precipitate formed and the color changed to pale brown. After cooling to room temperature, the solvents were evaporated under reduced pressure. The solid residue was dissolved in 15 % aqueous HCl (10 mL), the solution was extracted with chloroform (3 20 mL) and the combined organic layers were dried over MgSO 4 , filtered and concentrated in vacuum. Purification of the crude product affords DCTE 7a±10a.7a was prepared from aldehyde 3 in 93 % yield (40 mg) as an orange solid.1 H NMR spectroscopy indicated the product was pure enough to use without further purification. Mp = 102±104 C; 3, 92.6, 109.9, 112.6, 122.3, 124.4, 126.2, 129.0, 129.4, 132.5, 144.8, 145 21.7, 38.3, 93.0, 110.7, 123.2, 122.8, 126.0, 128.6, 129.4, 132.9, 142.6, 143.8, 167.4 84.5, 112.6, 113.0, 114.8, 115.3, 122.7, 123.2, 124.0, 125.9, 128.4, 129.3, 129.9, 132.2, 133.0, 143.1, 143.2, 159.5, 164.9