Synthesis of Helical Quinone Derivatives by Oxidative Coupling of Substituted 2-Hydroxybenzo[c]phenanthrenes
Abstract A concise synthesis of novel substituted quinone derivatives from commercially available starting materials was developed. For this synthesis, classical photo-induced 6π-electrocyclization was utilized, followed by oxidative aromatization reaction, and subsequent oxidative coupling reaction...
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Veröffentlicht in: | Synthesis (Stuttgart) 2017-04, Vol.49 (7), p.1547-1554 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Abstract
A concise synthesis of novel substituted quinone derivatives from commercially available starting materials was developed. For this synthesis, classical photo-induced 6π-electrocyclization was utilized, followed by oxidative aromatization reaction, and subsequent oxidative coupling reactions in the presence of CuCl(OH)-TMEDA. The unique quinone derivatives were characterized by IR,
1
H, and
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C NMR spectroscopies, and mass spectroscopic data analysis. In some cases, the keto dimers were obtained as significant intermediates for the quinone synthesis. |
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ISSN: | 0039-7881 1437-210X |
DOI: | 10.1055/s-0036-1588668 |