Facile Photochemical Synthesis of 5,10-Disubstituted [5]Helicenes by Removing Molecular Orbital Degeneracy
Author(s) -
Natsuki Ito,
Takashi Hirose,
Kenji Matsuda
Publication year - 2014
Publication title -
organic letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.94
H-Index - 239
eISSN - 1523-7060
pISSN - 1523-7052
DOI - 10.1021/ol5008718
Subject(s) - helicene , chemistry , knoevenagel condensation , yield (engineering) , antisymmetric relation , homo/lumo , molecular orbital , degeneracy (biology) , computational chemistry , photochemistry , excitation , molecule , combinatorial chemistry , organic chemistry , catalysis , quantum mechanics , bioinformatics , materials science , physics , metallurgy , mathematical physics , biology
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.
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