Hydroxymethylation hydroxylation of 1,3-diarylpropene through a catalytic diastereoselective Prins reaction: cyclization logic and access to brazilin core

A catalytic diastereoselective Prins reaction for hydroxymethylation and hydroxylation of 1,3-diarylpropene was successfully utilized to prepare various 1,3-dioxanes 7 in 14–88% yields. Take advantage of the synthetic intermediate 7h , the key B/C rings in brazilin core could be constructed by the s...

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Veröffentlicht in:Natural Products and Bioprospecting 2024-12, Vol.14 (1), p.29-29, Article 29
Hauptverfasser: Hu, Xin-Ting, Cheng, Qing-Yan, Chen, Yan-Ping, Li, Kun, Yan, Cai-Xian, Li, Dashan, Shao, Li-Dong
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Sprache:eng
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Zusammenfassung:A catalytic diastereoselective Prins reaction for hydroxymethylation and hydroxylation of 1,3-diarylpropene was successfully utilized to prepare various 1,3-dioxanes 7 in 14–88% yields. Take advantage of the synthetic intermediate 7h , the key B/C rings in brazilin core could be constructed by the sequential of Friedel–Crafts/Ullmann-Ma rather than Ullmann-Ma/Friedel–Crafts reactions. Graphical Abstract
ISSN:2192-2195
2192-2209
DOI:10.1007/s13659-024-00450-2