Enantioselective total synthesis of (-)-xialenon A.
The first total synthesis of (-)-xialenon A (1) via conjugate allylation of a 1,5-cyclooctadiene-derived bicyclo[3.3.0]octenone 3 and an alpha'-hydroxylation on the more hinderd face of enone 9 using hypervalent iodine chemistry, is described.
मुख्य लेखकों: | Hodgson, D, Galano, J, Christlieb, M |
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स्वरूप: | Journal article |
भाषा: | English |
प्रकाशित: |
2002
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समान संसाधन
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Enantioselective total synthesis of (-)-xialenon A.
द्वारा: Hodgson, D, और अन्य
प्रकाशित: (2002) -
Synthesis of (-)-xialenon A by enantioselective alpha-deprotonation-rearrangement of a meso-epoxide
द्वारा: Hodgson, D, और अन्य
प्रकाशित: (2003) -
Enantioselective access to isoquinuclidines by tropenone desymmetrization and homoallylic radical rearrangement: synthesis of (+)-ibogamine.
द्वारा: Hodgson, D, और अन्य
प्रकाशित: (2005) -
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प्रकाशित: (2020) -
Enantioselective total synthesis of (R)-(−)-complanine
द्वारा: Krystal A. D. Kamanos, और अन्य
प्रकाशित: (2012-10-01)