Access to 3-spiroindolizines containing an isoindole ring through intra-molecular arylation of spiro-N-acyliminium species: a new family of potent farnesyltransferase inhibitors

Author:

Pesquet Anthony12345,Marzag Hamid12345,Knorr Michael6789ORCID,Strohmann Carsten10111213,Lawson Ata Martin12345ORCID,Ghinet Alina1415161718ORCID,Dubois Joëlle192032122ORCID,Amaury Farce2324252627,Daïch Adam12345ORCID,Othman Mohamed12345

Affiliation:

1. Normandie Univ

2. UNILEHAVRE

3. CNRS

4. URCOM

5. 76600 Le Havre

6. Institut UTINAM-UMR CNRS 6213

7. Université Bourgogne Franche-Comté

8. 25030 Besançon

9. France

10. Anorganische Chemie

11. Technische Universität Dortmund

12. 44227 Dortmund

13. Germany

14. Faculty of Chemistry

15. ‘Al. I. Cuza’ University of Iasi

16. Iasi

17. Romania

18. Laboratoire de Pharmacochimie

19. Institut de Chimie des Substances Naturelles

20. UPR2301

21. Centre de Recherche de Gif

22. F-91198 Gif-sur-Yvette Cedex

23. Univ. Lille

24. Inserm

25. CHU Lille

26. U995-LIRIC-Lille Inflammation Research International Center

27. F-59000 Lille

Abstract

Based on N-acyliminium species, two efficient and rapid approaches to diversify spirocyclic systems connected by two different carbon centers to the isoindole ring have been developed.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference66 articles.

1. C. H. Heathcock , S. L.Graham , M. C.Pirrung , F.Plavac and C. T.White , Spirocyclic Systems , in The Total Synthesis of Natural Products , ed. J. A. Simon , John Wiley and Sons , New York , 1983 , vol. 5 , pp. 264

2. Stereocontrolled synthesis of spirocyclics

3. The chemistry of isatins: a review from 1975 to 1999

4. Paraherquamides, Brevianamides, and Asperparalines:  Laboratory Synthesis and Biosynthesis. An Interim Report

5. Recent advances in spirocyclization of indole derivatives

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