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Household Infrared Technology as an Energy-Efficient Approach to Achieve C-Cπ Bond Construction Reactions

We examined the ability of short-wave infrared (IR) light in the λ1.5-3.0 μm region of the infrared emission spectrum to accomplish C-Cπ bond construction reaction between π-excessive azaheteroaromatic and different carbonyl substrates supported on a bentonitic clay catalyst in solventless condition via a three-component condensation reaction. Preliminary studies show that the implementation of a domestic Flavor-Wave® oven fitted with a halogen heater lamp as a chemical reactor was as effective as the use of near IR light (λ1.1 μm) in fostering batch-wise organic reactions. Overall, this approach reveals its potential exploitation as an energy-efficient source to assemble biologically engaging (hetero)arenebisindolylmethanes framework, in the same way, that assure its sustainable development as for efficient generation of small libraries of molecules comparable to high-tech instrumentations performances.

Keywords:
electromagnetic radiation; (hetero)arenebisindolylmethane; bentonite tonsil-actisil FF (TAFF); Brønsted-Lowry acid


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