Substrate-Controlled Michael Additions of Chiral Ketones to Enones-Reference-Cited by-同舟云学术

Substrate-Controlled Michael Additions of Chiral Ketones to Enones

Published:2014-11-25 Issue:23 Volume:16 Page:6220-6223
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Fàbregas Mireia¹,Gómez-Palomino Alejandro¹,Pellicena Miquel¹,Reina Daniel F.¹,Romea Pedro¹,Urpí Fèlix¹,Font-Bardia Mercè²

Affiliation:

1. Departament de Química Orgànica and Institut de Biomedicina de la Universitat de Barcelona (IBUB), Universitat de Barcelona, Carrer Martí i Franqués 1-11, 08028 Barcelona, Catalonia, Spain

2. Unitat de Difracció de RX. CCiTUB, Universitat de Barcelona, Carrer Solé i Sabarís 1-3, 08028 Barcelona, Catalonia, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol503133j

Reference33 articles.

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2. bFeringa, B. L.; Jansen, J. F. G. A.InHouben-Weyl. Methods of Organic Chemistry;Helmchen, G., Hoffmann, R. W., Mulzer, J., Schaumann, E., Eds.Georg Thieme:Stuttgart, 1995; Vol.E21b; pp2104–2156.

3. A computational study of the 1,4-addition of lithium enolates to conjugated carbonyl compounds

4. Michael Addition of Stannyl Ketone Enolate to α,β-Unsaturated Esters Catalyzed by Tetrabutylammonium Bromide and an ab Initio Theoretical Study of the Reaction Course

5. Intermolecular Michael Reactions: A Computational Investigation

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