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Synfacts 2010(11): 1245-1245
DOI: 10.1055/s-0030-1258736
DOI: 10.1055/s-0030-1258736
Synthesis of Materials and Unnatural Products
© Georg Thieme Verlag
Stuttgart ˙ New York
Conjugate Additions When You Least Expect Them
X. Zhang, J. Li, H. Qu, C. Chi, J. Wu*
National University of Singapore, Singapore
Further Information
Publication History
Publication Date:
21 October 2010 (online)
Significance
Polyacenes have been extensively studied due to their potential application in electronic devices, such as organic field-effect transistors (OFETs) and organic light-emitting diodes (OLEDs). Due to decreasing solubility and stability as the acene length increases, peri-substituted polyacenes are often instead the targets for synthetic chemists. Synthesis of soluble and stable forms of these lengthy acenes typically involves the double nucleophilic addition of an organometallic reagent to the corresponding acenequinone, followed by aromatization of the formed diol.