Skip to content

Floris Chevallier

École Normale Supérieure de Lyon
Menu
  • Home
  • Scientific Background
  • Research
  • Teaching

30. Deprotonative Metalation of Aromatic Compounds Using Mixed Lithium-Iron Combinations.

https://doi.org/10.1016/j.tet.2012.02.019

E. Nagaradja, F. Chevallier, T. Roisnel, V. Jouikov, F. Mongin, Tetrahedron 2012, 68, 3063-3073.

29. Chiral Organomagnesiates as Dual Reagents for Bromine-Magnesium Exchange of 2-Bromopyridine and Access to Chiral α-Substituted 2-Pyridylcarbinols.

https://doi.org/10.1002/ejoc.201101490

D. Catel, F. Chevallier, F. Mongin, P. C. Gros, Eur. J. Org. Chem. 2012, 53-57.

28. Deprotonative Metalation of Chloro- and Bromopyridines Using Amido-Based Bimetallic Species and Regioselectivity-Computed CH Acidity Relationships.

https://doi.org/10.1002/chem.201101993

K. Snégaroff, T. T. Nguyen, N. Marquise, Y. S. Halauko, P. J. Harford, T. Roisnel, V. E. Matulis, O. A. Ivashkevich, F. Chevallier, A. E. H. Wheatley, P. C. Gros, F. Mongin, Chem. Eur. J. 2011, 17, 13284-13297.

27. Deprotonative Metalation of Aromatic Compounds by Using an Amino-Based Lithium Cuprate.

https://doi.org/10.1002/chem.201100990

T. T. Nguyen, N. Marquise, F. Chevallier, F. Mongin, Chem. Eur. J. 2011, 17, 10405-10416.

26. syn-Allylstannation of N-Acyliminium Intermediates by Tributyl[γ-(silyloxy)allyl]stannanes: A Key Reaction for the Diastereoselective Synthesis of Polyhydroxypiperidines and Polyhydroxyazepanes.

https://doi.org/10.1002/ejoc.201100302

F. Chevallier, A. Lumbroso, I. Beaudet, E. Le Grognec, L. Toupet, J.-P. Quintard, Eur. J. Org. Chem. 2011, 4133-4144.

25. N-Aryl Pyrazoles: DFT Calculations of CH Acidity and Deprotonative Metallation Using a Combination of Lithium and Zinc Amides.

https://doi.org/10.1039/c1ob05267e

F. Chevallier, Y. S. Halauko, C. Pecceu, I. F. Nassar, T. U. Dam, T. Roisnel, V. E. Matulis, O. A. Ivashkevich, F. Mongin, Org. Biomol. Chem. 2011, 9, 4671-4684.

24. Diastereoselective Deprotonative Metalation of Sugar-Derived Ferrocene Esters Using Mixed Lithium-Cadmium Combinations.

https://doi.org/10.1002/ejoc.201100264

A. Sreeshailam, G. Dayaker, F. Chevallier, T. Roisnel, P. Radha Krishna, F. Mongin, Eur. J. Org. Chem. 2011, 3715-3718.

23. Deprotonative Metalation of Substituted Aromatics Using Mixed Lithium-Cobalt Combinations.

https://doi.org/10.1016/j.tet.2010.09.053

G. Dayaker, F. Chevallier, P. C. Gros, F. Mongin, Tetrahedron 2010, 66, 8904-8910.

22. Homoleptic Zincate-Promoted Room-Temperature Halogen-Metal Exchange of Bromopyridines.

https://doi.org/10.1002/chem.201001664

N. T. T. Chau, M. Meyer, S. Komagawa, F. Chevallier, Y. Fort, M. Uchiyama, F. Mongin, P. C. Gros, Chem. Eur. J. 2010, 16, 12425-12433.

21. Deprotonative Metalation of Substituted Benzenes and Heteroaromatics Using Amino/Alkyl Mixed Lithium-Zinc Combinations.

https://doi.org/10.1002/chem.201000543

K. Snégaroff, S. Komagawa, F. Chevallier, P. C. Gros, S. Golhen, T. Roisnel, M. Uchiyama, F. Mongin, Chem. Eur. J. 2010, 16, 8191-8201.

Posts navigation

Older posts
Newer posts

Floris Chevallier
Building #M6 – Office #144
Tel. +33 (0)4 72 72 87 33

Tweets by Laboratoide de chimie
© 2025 Floris Chevallier | WordPress Theme by Superb Themes
Back to Top ↑