![](https://perso.ens-lyon.fr/floris.chevallier/wp-content/uploads/2021/06/40-1.jpg)
https://doi.org/10.1021/ol401803t
A. S. Trita, T. Roisnel, F. Mongin, F. Chevallier, Org. Lett. 2013, 15, 3798-3801.
https://doi.org/10.1021/ol401803t
A. S. Trita, T. Roisnel, F. Mongin, F. Chevallier, Org. Lett. 2013, 15, 3798-3801.
https://doi.org/10.1016/j.tetlet.2013.04.020
N. Marquise, P. J. Harford, F. Chevallier, T. Roisnel, A. E. H. Wheatley, P. C. Gros, F. Mongin, Tetrahedron Lett. 2013, 54, 3154-3157.
https://doi.org/10.1002/chem.201300552
R. R. Kadiyala, D. Tilly, E. Nagaradja, T. Roisnel, V. E. Matulis, O. A. Ivashkevich, Y. S. Halauko, F. Chevallier, P. C. Gros, F. Mongin, Chem. Eur. J. 2013, 19, 7944-7960.
https://doi.org/10.1007/7081_2012_92
F. Chevallier, F. Mongin, in Topics in Heterocyclic Chemistry, Vol. 31, (Eds.: M. Schnürch, M. D. Mihovilovic), Springer-Verlag, Berlin, Heidelberg, 2013, pp. 93-129.
https://doi.org/10.1016/j.tetasy.2012.11.003
O. Payen, F. Chevallier, F. Mongin, P. C. Gros, Tetrahedron: Asymmetry 2012, 23, 1678-1682.
https://doi.org/10.1016/j.tet.2012.08.008
D. Tilly, K. Snégaroff, G. Dayaker, F. Chevallier, P. C. Gros, F. Mongin, Tetrahedron 2012, 68, 8761-8766.
https://doi.org/10.1002/ejoc.201200965
G. Dayaker, D. Tilly, F. Chevallier, G. Hilmersson, P. C. Gros, F. Mongin, Eur. J. Org. Chem. 2012, 6051-6057.
https://doi.org/10.1039/c2ra21045b
A. Sreeshailam, G. Dayaker, D. V. Ramana, F. Chevallier, T. Roisnel, S. Komagawa, R. Takita, M. Uchiyama, P. Radha Krishna, F. Mongin, RSC Adv. 2012, 2, 7030-7032.
https://doi.org/10.1039/c2ob25554e
F. Chevallier, T. Blin, E. Nagaradja, F. Lassagne, T. Roisnel, Y. S. Halauko, V. E. Matulis, O. A. Ivashkevich, F. Mongin, Org. Biomol. Chem. 2012, 10, 4878-4885.
https://doi.org/10.1016/j.tet.2012.03.058
D. Catel, O. Payen, F. Chevallier, F. Mongin, P. C. Gros, Tetrahedron 2012, 68, 4018-4028.