Bismuth triflate-catalyzed Wagner-Meerwein rearrangement in terpenes. Application to the synthesis of the 18α-oleanane core and A-neo-18α-oleanene compounds from lupanes-Reference-Cited by-同舟云学术

Bismuth triflate-catalyzed Wagner-Meerwein rearrangement in terpenes. Application to the synthesis of the 18α-oleanane core and A-neo-18α-oleanene compounds from lupanes

Published:2009 Issue:3 Volume:7 Page:508-517
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Salvador Jorge A. R.,Pinto Rui M. A.,Santos Rita C.,Le Roux Christophe,Beja Ana Matos,Paixão José A.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2009/OB/B814448F

Reference67 articles.

1. The function of terpene natural products in the natural world

2. Terpenes: substances useful in human healthcare

3. J. F. King and P.Mayo, Terpenoid Rearrangements, in Molecular Rearrangements, ed. P. Mayo, Interscience Publishers, John Wiley & Sons, New York, 1968, pp. 771-840

4. J. R. Hanson , Wagner–Meerwein Rearrangements, in Comprehensive Organic Synthesis, ed. P. G., Pergamon Press plc, Oxford, 1991, pp. 705-719

5. Chemistry, biological activity, and chemotherapeutic potential of betulinic acid for the prevention and treatment of cancer and HIV infection

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