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 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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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 |
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ISSN: | 2192-2195 2192-2209 |
DOI: | 10.1007/s13659-024-00450-2 |