Stereoselective Conjugate Addition of Aryl- and Alkenylboronic Acids to Acyclic γ,δ-Oxygen-Substituted α,β-Enoates

Author:

Segura Amaya1,Csákÿ Aurelio G.1

Affiliation:

1. Departamento de Química Orgánica, Facultad de Química, Universidad Complutense, 28040-Madrid, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference13 articles.

1. Rhodium-Catalyzed Conjugate Addition of Aryl- or 1-Alkenylboronic Acids to Enones

2. Reviews:  (a) Hayashi, T.Synlett2001, 879. (b) Fagnou, K.; Lautens, M.Chem. Rev.2003,103, 169. (c) Hayashi, T.; Yamasaki, K.Chem. Rev.2003,103, 2829. (d) Hayashi, T.Pure Appl. Chem.2004,76, 465. (e) Hayashi, T.Bull. Chem. Soc. Jpn.2004,77, 13. (f) Yoshida, K.; Hayashi, T. InModern Rhodium-Catalyzed Organic Reactions; Evans, P. A., Ed.; Wiley-VCH:  Weinheim, Germany, 2005; Chapter 3, p 55.

3. Di(isopropylprenyl)borane: A New Hydroboration Reagent for the Synthesis of Alkyl and Alkenyl Boronic Acids

4. Enantioselective 1,4-addition of arylboronic acids to α,β-unsaturated carbonyl compounds catalyzed by rhodium(I)-chiral phosphoramidite complexes

5. Stereoselective C-Glycoside Formation by a Rhodium(I)-Catalyzed 1,4-Addition of Arylboronic Acids to Acetylated Enones Derived from Glycals

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