Aromatic Heterocycles as Activating Groups for Asymmetric Conjugate Addition Reactions. Enantioselective Copper-Catalyzed Reduction of 2-Alkenylheteroarenes-Reference-Cited by-同舟云学术

Aromatic Heterocycles as Activating Groups for Asymmetric Conjugate Addition Reactions. Enantioselective Copper-Catalyzed Reduction of 2-Alkenylheteroarenes

Published:2009-07-09 Issue:30 Volume:131 Page:10386-10387
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Rupnicki Leszek¹,Saxena Aakarsh¹,Lam Hon Wai¹

Affiliation:

1. School of Chemistry, University of Edinburgh, Joseph Black Building, The King’s Buildings, West Mains Road, Edinburgh EH9 3JJ, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja904365h

Reference55 articles.

1. For recent reviews focused on metal-catalyzed enantioselective conjugate addition reactions, see:

2. Copper-Catalyzed Asymmetric Michael Addition of Magnesium, Zinc, and Aluminum Organometallic Reagents: Efficient Synthesis of Chiral Molecules

3. Recent Advances in Metal-Catalyzed Asymmetric Conjugate Additions

4. Catalytic Enantioselective Conjugate Addition with Grignard Reagents

5. Rhodium-Catalyzed Asymmetric 1,4-Addition and Its Related Asymmetric Reactions

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