A novel and efficient one-pot method has been developed for the synthesis of cyclopropane-fused bicyclic amidines on the basis of a CuBr -mediated oxidative cyclization of carbanions. The usefulness of this unique multicomponent strategy has been demonstrated by the use of a wide variety of substrates to furnish novel cyclopropane-containing amidines with a quaternary center in very good yields. This ketenimine-based approach provides straightforward access to biologically active and pharmaceutically important 3-azabicyclo[n.1.0]alkane frameworks under mild conditions. The synthetic power of this methodology is exemplified in the concise synthesis of the pharmaceutically important antidepressant drug candidate GSK1360707 and key intermediates for the synthesis of amitifadine, bicifadine, and narlaprevir.

Calcium oxide was used as photocatalyst for the degradation of indigo carmine dye solution in the visible, long UV, and short UV radiation. We have investigated the effectiveness of degradation of indigo carmine dye solution at pH 9 and 12 using calcium oxide with the particle size of 30-36 nm by varying the concentration, dose of adsorbent, and duration. It has been found that the degradation of indigo carmine dye is effective at pH = 9, when 0.12 g of calcium oxide was used. The nature of interaction between calcium oxide and indigo carmine dye was discussed.

A one-pot catalytic method has been developed for the stereoselective synthesis of cyclopropane-fused cyclic amidines using CuBr2/K2S2O8 as an efficient single electron transfer (SET) oxidative system. The generality of this...

Stereoselective synthesis of 3-azabicyclo[n.1.0]alkane by silver oxide catalyzed SET oxidative cyclization.

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