Synthesis of Bisflavanol-Type Natural Products and Their Analogues­ via Self-Coupling of C8-Methylol Catechin Derivatives

Abstract A highly efficient and regioselective self-coupling of C8-methylol catechin derivatives is developed for the synthesis of dimeric flavanol analogues under metal-free and mild conditions. Its applicability is showcased by the efficient synthesis of bisflavanol-type natural products bis-8,8′-...

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Veröffentlicht in:Synthesis (Stuttgart) 2019-08, Vol.51 (16), p.3127-3141
Hauptverfasser: Huang, Deng-Ming, Li, Hui-Jing, Zhao, Yan, Wu, Yan-Chao
Format: Artikel
Sprache:eng
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Zusammenfassung:Abstract A highly efficient and regioselective self-coupling of C8-methylol catechin derivatives is developed for the synthesis of dimeric flavanol analogues under metal-free and mild conditions. Its applicability is showcased by the efficient synthesis of bisflavanol-type natural products bis-8,8′-catechinylmethane, bis-8,8′-epicatechinylmethane, talienbisflavan A, and oolonghomobisflavan A. The novel self-coupling mechanism sheds new light on the classical Friedel–Crafts alkylation mechanism in acid-catalyzed catechin–formaldehyde condensation.
ISSN:0039-7881
1437-210X
DOI:10.1055/s-0037-1610707