Synthesis of (-)-xialenon A by enantioselective alpha-deprotonation-rearrangement of a meso-epoxide
The first total synthesis of (-)-xialenon A was achieved via enantioselective transannular desymmetrisation of a substituted cycloctene oxide using an organolithium/(-)-α-isosparteine combination. Oxidation of the resulting bicyclo[3.3.0]octanol gave an enone which underwent stereoselective conjugat...
मुख्य लेखकों: | Hodgson, D, Galano, J, Christlieb, M |
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स्वरूप: | Journal article |
भाषा: | English |
प्रकाशित: |
2003
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समान संसाधन
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Enantioselective alpha-deprotonation-rearrangement of meso-epoxides
द्वारा: Hodgson, D, और अन्य
प्रकाशित: (1996) -
Functionalised bicyclic alcohols by enantioselective alpha-deprotonation-rearrangement of meso-epoxides
द्वारा: Hodgson, D, और अन्य
प्रकाशित: (2001) -
Enantioselective total synthesis of (-)-xialenon A.
द्वारा: Hodgson, D, और अन्य
प्रकाशित: (2002) -
Enantioselective total synthesis of (-)-xialenon A.
द्वारा: Hodgson, D, और अन्य
प्रकाशित: (2002) -
Enantioselective alpha-deprotonation of epoxides.
द्वारा: Hodgson, D
प्रकाशित: (2001)