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Functionalization of a non activated CH bond: Fluorination of vindoline at C-20 in superacids

DOI

16

Citations

8

References

1998

Year

C. Berrier, Jean‐Claude Jacquesy, Marie‐Paule Jouannetaud, Ce ́cile Lafitte, Yves Vidal, Fabien Zunino, Jacques Fahy, Alain Duflos
Tetrahedron

References

YearCitations

Application of a modification of the Polonovski reaction to the synthesis of vinblastine-type alkaloids

Nicole Langlois, Françoise Guéritte, Yves Langlois,

Journal of the American Chemical Society

1976

223

Production of 3', 4'-anhydrovinblastine: a unique chemical synthesis

John Vukovic, Anne E. Goodbody, J. P. KUTNEY,

Tetrahedron

1988

87

Correlation of biologic data with physico-chemical properties among the Vinca alkaloids and their congeners

Richard J. Owellen, Douglas W. Donigian, Carol Hartke,

Biochemical Pharmacology

1977

56

Synthesis of hexacyclic indole alkaloids related to vindolinine by sonochemical cyclization

Georgette Hugel, Dominique Cartier, Jean Lévy

Tetrahedron Letters

1989

19

The 3,3-dimethyl-1-butyl cation

Philip S. Skell, Paul H. Reichenbacher

Journal of the American Chemical Society

1968

19

Synthesis of fluorohydrins and of bromofluoroderivatives by anti addition on the 14,15 Double bond of tabersonine in superacids

C. Berrier, J. C. JACQUESY, Marie‐Paule Jouannetaud,

Tetrahedron

1990

15

Protonated cyclopropanes. II. The solvolysis of cyclopropane in tritiated sulfuric acid

C. C. Lee, L. Gruber

Journal of the American Chemical Society

1968

14

Direct bromination or hydroxylation at C-11 in vincadifformine and tabersonine derivatives in superacids

C. Berrier, J. C. JACQUESY, Marie‐Paule Jouannetaud,

Tetrahedron

1990

11

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