The reaction of hyperforin with hydride reducing agents.
Författare
Summary, in English
As part of a study aimed at generating analogues of hyperforin (1), the reaction of this prenylated phloroglucinol with various hydride reducing agents was investigated. Hyperforin contains two beta-dicarbonyl systems, one of which is non-enolizable, and it was interesting to assess the relative reactivity of these structural elements in the highly compact framework of the natural product. Depending on the reducing agent employed, a surprising range of compounds could be obtained, sometimes in synthetically useful yields. The stereochemistry of the LiAlH4-reduced product was secured by X-ray analysis and served as a base for elucidating the configuration of a series of reduced and deoxygenated analogues obtained with other reducing agents. The chemoselectivity observed in these reactions is apparently the result of a combination of metal-chelation and hydrogen-bonding effects.
Avdelning/ar
Publiceringsår
2006
Språk
Engelska
Sidor
5479-5484
Publikation/Tidskrift/Serie
European Journal of Organic Chemistry
Dokumenttyp
Artikel i tidskrift
Förlag
John Wiley & Sons Inc.
Ämne
- Organic Chemistry
Nyckelord
- acylphloroglucinols
- natural products
- reduction
Status
Published
ISBN/ISSN/Övrigt
- ISSN: 1434-193X