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
Hauptverfasser: Shahabuddin, Mohammad, Akutsu, Akira, Kimura, Takao, Karikomi, Michinori
Format: Artikel
Sprache:eng
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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 13 C NMR spectroscopies, and mass spectroscopic data analysis. In some cases, the keto dimers were obtained as significant intermediates for the quinone synthesis.
ISSN:0039-7881
1437-210X
DOI:10.1055/s-0036-1588668