Triflimide (HNTf2)–catalyzed aldehyde cross-aldol reaction using “super silyl” enol ethers
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Biochemistry, Genetics and Molecular Biology
Link
http://www.nature.com/articles/nprot.2006.389.pdf
Reference12 articles.
1. Yanigisawa, A., Ishihara, K. & Yamamoto, H. Asymmetric protonation of enol derivatives. Synlett (suppl. 1): 411–420 (1997).
2. Saito, S. & Yamamoto, H. Design of acid-base catalysis for the asymmetric direct aldol reaction. Acc. Chem. Res. 37, 570–579 (2004).
3. Bolm, C., Rantanen, T., Schiffers, I. & Zani, L. Protonated chiral catalysts: Versatile tools for asymmetric synthesis. Angew. Chem. Int. Ed. 44, 1758–1763 (2005).
4. Ishihara, K., Hiraiwa, Y. & Yamamoto, H. A high yield procedure for the me3sintf2-induced carbon-carbon bond-forming reactions of silyl nucleophiles with carbonyl compounds: the importance of additions order and solvent effects. Synlett 1851–1854 (2001).
5. Boxer, M.B. & Yamamoto, H. Tris(trimethylsilyl)silyl-governed aldehyde cross-aldol cascade reaction. J. Am. Chem. Soc. 128, 48–49 (2006).
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