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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.

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Spelling suggestions: "subject:"norsesquiterpene"" "subject:"furanosesquiterpene""

1

Rapid stereoselective access to the tetracyclic core of puupehenone and related sponge metabolites using metal-free radical cyclisations of cyclohexenyl-substituted 3-bromochroman-4-ones.

Pritchard, R.P., Sheldrake, Helen M., Taylor, I.Z., Wallace, T.W. 23 June 2008 (has links)
No / The tetracyclic nucleus of puupehenone, 15-oxopuupehenol and other sesquiterpene¿phenol natural products can be assembled stereoselectively in three steps, the last of these being the 6-endo-trig cyclisation of an alpha-keto radical generated from a substituted 2-(2-cyclohexenyl)ethyl 3-bromo-4-chromanone under metal-free conditions. / EPSRC
Natural products
Sesquiterpene¿phenol
Merosesquiterpene
Benzo[a]xanthene
Puupehenone
Radical cyclisation
6-endo-Trig

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