I2-Catalyzed enantioselective ring expansion of β-lactams to γ-lactams through a novel C3–C4 bond cleavage. Direct entry to protected 3,4-dihydroxypyrrolidin-2-one derivatives-Reference-Cited by-同舟云学术

I2-Catalyzed enantioselective ring expansion of β-lactams to γ-lactams through a novel C3–C4 bond cleavage. Direct entry to protected 3,4-dihydroxypyrrolidin-2-one derivatives

Published:2008 Issue:5 Volume: Page:615-617
ISSN:1359-7345
Container-title:Chem. Commun.
language:en
Short-container-title:Chem. Commun.

Author:

Alcaide Benito,Almendros Pedro,Cabrero Gema,Ruiz M. Pilar

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2008/CC/B715661H

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2. Pyrrole, pyrrolidine, pyridine, piperidine and tropane alkaloids (1998 to 1999)

3. J. W. Daly , H. M.Garraffo and T. F.Spende, in Alkaloids: Chemical and Biological Perspectives, ed. S. W. Pelletier, Pergamon, New York, 1999, vol. 13, ch. 1

4. Chiral amines as organocatalysts for asymmetric conjugate addition to nitroolefins and vinyl sulfones via enamine activation

5. Diarylprolinol Ethers: Expanding the Potential of Enamine/Iminium-Ion Catalysis

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