Two remarkable epimerizations imperative for the success of an asymmetric total synthesis of (+)-aigialospirol
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Publisher
Springer Science and Business Media LLC
Subject
General Chemistry
Link
http://link.springer.com/content/pdf/10.1007/s11426-010-4176-8.pdf
Reference74 articles.
1. For a reviews, see; (a) Mukaiyama T, Murakami M. Cross-coupling reactions based on acetals. Synthesis, 1987: 1043–1054
2. Alexakis A, Mangeney P. Chiral acetals in asymmetric synthesis. Tetrahedron Asy, 1990, 1: 477–511
3. Also see: Harmata M, Rashatasakhon P. Cycloaddition reactions of vinyl oxocarbenium ions. Tetrahedron, 2003, 59: 2371–2395
4. Ko C, Feltenberger JB, Ghosh SK, Hsung RP. Gassman’s intramolecular [2+2] cationic cycloaddition. Formal total syntheses of raikovenal and epi-raikovenal. Org Lett, 2008, 10: 1971–1974
5. For reviews, see: (a) Aho JE, Pihko PM, Rissa TK. Nonanomeric spiroketals in natural products: Structures, sources, and synthetic Strategies. Chem Rev, 2005, 105: 4406–4440
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