Rearrangement of quinine in superacid: an efficient access to a novel chiral heterocyclic system-Reference-Cited by-同舟云学术

Rearrangement of quinine in superacid: an efficient access to a novel chiral heterocyclic system

Published:2002-11 Issue:48 Volume:43 Page:8773-8775
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Thibaudeau Sébastien,Violeau Bruno,Martin-Mingot Agnès,Jouannetaud Marie-Paule,Jacquesy Jean-Claude

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Olah, G. A.; Prakash, G. K. S.; Sommer, J. Superacids; Wiley Interscience: New York, 1985; Chapter 5, pp. 243–344.

2. Jacquesy, J. C. In Stable Carbocation Chemistry; Prakash, G. K. S.; Schleyer, P. v. R., Eds.; Wiley Interscience: New York, 1997; Chapter 17, pp. 549–574.

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

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

5. Rearrangement of vindoline and derivatives in superacidic media

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