Tandem Enantioselective Conjugate Addition−Cyclopropanation. Application to Natural Products Synthesis
Author:
Affiliation:
1. Department of Organic Chemistry, University of Geneva, 30 quai Ernest-Ansermet, Geneva 4, Switzerland CH-1211
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo026262w
Reference41 articles.
1. For recent reviews see: (a) Alexakis, A.; Benhaim, C.Eur. J. Org.Chem.2002, 3221. (b) Krause, N.; Hoffmann-Röder, A.Synthesis2001, 171. (c) Sibi, M. P.; Manyem, S.Tetrahedron2000,56, 8033. (d) Tomioka, K.; Nagaoka, Y. InComprensive Asymmetric Catalysis I−III; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: New York, 1999; p 1105.
2. Copper-mediated asymmetric transformations
3. Efficient Cu-Catalyzed Asymmetric Conjugate Additions of Alkylzincs to Trisubstituted Cyclic Enones
4. Modular Peptide-Based Phosphine Ligands in Asymmetric Catalysis: Efficient and Enantioselective Cu-Catalyzed Conjugate Additions to Five-, Six-, and Seven-Membered Cyclic Enones
5. Novel Biphenol Phosphoramidite Ligands for the Enantioselective Copper-Catalyzed Conjugate Addition of Dialkyl zincs
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