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- W2897726982 abstract "π-Conjugated molecules are the active materials in organic electronics, yet the range of available materials is limited by the nontrivial, multistep synthetic process required to obtain long π-conjugated backbones. Here, Diels–Alder cycloaddition and its reactivity and selectivity are evaluated as a means for obtaining long, novel, π-conjugated backbones. Particular attention is paid to the Diels–Alder conjugation products of furans, such as selectively substituted arenes and, potentially, carbon nanoribbons. 1 Introduction 2 Aromatic Transformations by Diels–Alder Cycloaddition 3 The Question of Regioselectivity 4 Outlook" @default.
- W2897726982 created "2018-10-26" @default.
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- W2897726982 date "2018-10-09" @default.
- W2897726982 modified "2023-09-25" @default.
- W2897726982 title "Multiple Diels–Alder Transformations in Linear π-Conjugated Systems" @default.
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- W2897726982 doi "https://doi.org/10.1055/s-0037-1610301" @default.
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