Catalytic enantioselective formation of chiral-bridged dienes which are themselves ligands for enantioselective catalysis
- PMID: 19947622
- PMCID: PMC2814301
- DOI: 10.1021/ol9025793
Catalytic enantioselective formation of chiral-bridged dienes which are themselves ligands for enantioselective catalysis
Abstract
This paper reports a method for highly enantioselective Diels-Alder reaction with an acetylene equivalent to produce chiral-bridged dienes. These dienes, by coordination to Rh(I), can serve as catalysts for the enantioselective addition of vinyl or aryl groups to alpha,beta-unsaturated ketones.
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- Corey EJ, Lee TW. Tetrahedron Lett. 1997;38:5755–5758.
- Ishihara K, Kondo S, Kurihara H, Yamamoto H. J. Org. Chem. 1997;62:3026–3027. - PubMed
- Evans DA, Miller SJ, Lectka T, Matt PV. J. Am. Chem. Soc. 1999;121:7559–7573.
- Ishihara K, Fushimi M. J. Am. Chem. Soc. 2008;130:7532–7533. - PubMed
- Payette JN, Yamamoto H. Angew. Chem., Int. Ed. 2009;48:8060–8062. - PMC - PubMed
-
-
For reviews regarding diene-based ligands, see: Johnson JB, Rovis T. Angew. Chem., Int. Ed. 2008;47:840–871. Defieber C, Grutzmacher H, Carreira EM. Angew. Chem., Int. Ed. 2008;47:4482–4502.
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Initial studies on the synthesis of the diene framework by Diels-Alder cycloaddition of dienes to alkyne-based dieneophiles were discontinued because only moderate enantioselectivities were observed.
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- Hayashi T, Yamasaki K. Chem. Rev. 2003;103:2829–2844. - PubMed
- Hayashi T. Bull. Chem. Soc. Jpn. 2004;77:13–21.
- Christoffers J, Koripelly G, Rosiak A, Rössle M. Synthesis. 2007:1279–1300.
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