Enantioselective Enolate Protonation:  Matching Chiral Aniline and Substrate Acidity

Author:

Vedejs E.1,Kruger A. W.1,Suna E.1

Affiliation:

1. Chemistry Department, University of Wisconsin, Madison Wisconsin 53706

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Reference29 articles.

1. Deracemization via Highly Enantioselective Enolate Protonation Using a Chiral Aniline as the "Acid"

2. (c) Asensio, G.; Aleman, P.; Cuenca, A.; Gil, J.; Medio-Simon, M.Tetrahedron: Asymmetry1998,9, 4073. Takeuchi, S.; Nakamura, Y.; Ohgo, Y.; Curran, D. P.Tetrahedron Lett.1998,39, 8691. Asensio, G.; Aleman, P.; Gil, J.; Domingo, L. R.; Medio-Simon, M.J. Org. Chem.1998,63, 9342. Yanagisawa, A.; Kikuchi, T.; Kuribayashi, T.; Yamamoto, H.Tetrahedron1998,54, 10253. Yanagisawa, A.; Inanami, H.; Yamamoto, H.J. Chem. Soc.Chem. Commun.1998, 1573. Aboulhoda, S. J.; Reiners, I.; Wilken, J.; Henin, F.; Martens, J.; Muzart, J.Tetrahedron:  Asymmetry1998,9, 1847. Mikami, K.; Yamaoka, M.; Yoshida, A.Synlett1998, 607. Yanagisawa, A.; Ishihara, K.; Yamamoto, H.Synlett1997, 411 and references therein.

3. Enantioselective protonation of amide enolates derived from piperidine-2-carboxylic acid

4. Structure and Reactivity of Lithium Enolates. From Pinacolone to SelectiveC-Alkylations of Peptides. Difficulties and Opportunities Afforded by Complex Structures

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