SmI2-Mediated Cyclizations of Derivatized β-Lactams for the Highly Diastereoselective Construction of Functionalized Prolines

Author:

Jacobsen Mikkel F.1,Turks Maris1,Hazell Rita1,Skrydstrup Troels1

Affiliation:

1. Department of Chemistry, University of Aarhus, Langelandsgade 140, 8000 Aarhus C, Denmark

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Reference36 articles.

1. For recent reviews on the application of SmI2in organic synthesis:  (a) Krief, A.; Laval, A.M.Chem. Rev.1999,99, 745. (b) Molander, G. A.; Harris, C. R.Chem. Rev.1996,96, 307. (c) Molander, G. A.; Harris, C. R.Tetrahedron1998,54, 3321. (d) Skrydstrup, T.Angew. Chem., Int. Ed. Engl.1997,36, 345. (e) Molander G. A. InOrganic Reactions; Paquette, L. A., Ed.; John Wiley:  New York, 1994; Vol. 46, p 211. (f) Imamoto, T.Lanthanides in Organic Synthesis; Academic Press:  London, 1994. (g) Molander, G. A.Chem. Rev.1992,92, 29. (h) Curran, D. P.; Fevig, T. L.; Jaspersen, C. P.; Totleben, M. L.Synlett1992, 943.

2. Application of Reductive Samariation to the Synthesis of Small Unnatural Peptides

3. Selective Side Chain Introduction onto Small Peptides Mediated by Samarium Diiodide:  A Potential Route to Peptide Libraries

4. (a) Tamburini, B.; Perboni, A.; Rossi, T.; Donati, D.; Gaviraghi, G.; Tarzia, G. InRecent Advances in the Chemistry of Anti-Infective Agents; Bentley, P. H., Ponsford, R., Eds.; Royal Society of Chemistry:  Cambridge, 1992; p 21.

5. The renewed challenge of antibacterial chemotherapy†

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