Facile photochemical synthesis of 5,10-disubstituted [5]helicenes by removing molecular orbital degeneracy

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Abstract

Photocyclodehydrogenation is a key reaction to synthesize helicenes; however, because of overannulation, it is not applicable to the synthesis of [5]helicene. Introduction of a cyano group was found to remove the orbital degeneracy of the low-lying unoccupied MOs; consequently, the lowest excitation comprises a single transition involving the C2-antisymmetric MO. Therefore, the problematic overannulation can be effectively suppressed. Moreover, in combination with the Knoevenagel reaction, a one-pot synthesis of 5,10-dicyano[5]helicene with 67% yield was accomplished. © 2014 American Chemical Society.

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Ito, N., Hirose, T., & Matsuda, K. (2014). Facile photochemical synthesis of 5,10-disubstituted [5]helicenes by removing molecular orbital degeneracy. Organic Letters, 16(9), 2502–2505. https://doi.org/10.1021/ol5008718

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