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.
Egile Nagusiak: | Hodgson, D, Galano, J, Christlieb, M |
---|---|
Formatua: | Journal article |
Hizkuntza: | English |
Argitaratua: |
2002
|
Antzeko izenburuak
-
Enantioselective total synthesis of (-)-xialenon A.
nork: Hodgson, D, et al.
Argitaratua: (2002) -
Synthesis of (-)-xialenon A by enantioselective alpha-deprotonation-rearrangement of a meso-epoxide
nork: Hodgson, D, et al.
Argitaratua: (2003) -
Enantioselective access to isoquinuclidines by tropenone desymmetrization and homoallylic radical rearrangement: synthesis of (+)-ibogamine.
nork: Hodgson, D, et al.
Argitaratua: (2005) -
Enantioselective total synthesis of (-)-deoxoapodine
nork: Kang, Taek, et al.
Argitaratua: (2020) -
Enantioselective total synthesis of (R)-(−)-complanine
nork: Krystal A. D. Kamanos, et al.
Argitaratua: (2012-10-01)