-2016-

Synthesis of Fluoroalkyl Pyrazoles from In-Situ-Generated C2F5CHN2 and Electron-Deficient Alkenes
P.K. Mykhailiuk, A.Y. Ishchenko, V. Stepanenko, J. Cossy
Eur. J. Org. Chem. 2017, 5485. DOI : 10.1002/ejoc.201600947
https://https://hal.archives-ouvertes.fr/hal-03229286v1

Iron-Catalyzed C–C Cross-Couplings Using Organometallics
A. Guérinot, J. Cossy
Top. Curr. Chem. 2016, 374, 49. DOI : 10.1007/s41061-016-0047-x
https://https://hal.archives-ouvertes.fr/hal-03229287v1

Selective Tsuji-Trost type C-allylation of hydrazones : A straightforward entry into 4,5-dihydropyrazoles.
H. Elhachemia, M. Cattoen, M. Cordier, J. Cossy, S. Arseniyadis, H. Ilitkie, L. El Kaïm
Chem. Commun. 2016, 52, 14490-14493. DOI : 10.1039/C6CC08171A
https://https://hal.archives-ouvertes.fr/hal-01623194v1

Elaboration of sterically hindered delta-lactones through ring-closing metathesis : Application to the synthesis of the C1-C27 fragment of hemicalide
C. Lecourt, S. Boinapally, S. Dhambri, G. Boissonnat, C. Meyer, J. Cossy, F. Sautel, G. Massiot, J. Ardisson, G. Sorin, M.-I. Lannou
J. Org. Chem. 2016, 81, 12275-12290. DOI : 10.1021/acs.joc.6b02208
https://https://hal.archives-ouvertes.fr/hal-02370458v1

Unexpected reactivity of trifluoromethyl diazomethane (CF3CHN2) : Electrophilicity of the terminal N-atom
A. V. Arkhipov, V. V. Arkhipov, J. Cossy, V. O. Kovtunenko, P. K. Mykhailiuk
Org. Lett. 2016, 18, 3406-3409. DOI : 10.1021/acs.orglett.6b01565
https://https://hal.archives-ouvertes.fr/hal-03229288v1

Synthetic studies toward the C14−C29 fragment of mirabalin.
J. Cornil, P.-G. Echeverria, S. Reymond, P. Phansavath, V. Ratovelomanana-Vidal, A. Guérinot, J. Cossy
Org. Lett. 2016, 18, 4534-4537. DOI : 10.1021/acs.orglett.6b02162
https://https://hal.archives-ouvertes.fr/hal-03229297v1

Synthesis of the Acyclic Carbon Skeleton of Filipin III
E. Brun, V. Bellosta, J. Cossy
J. Org. Chem. 2016, 81, 8206-8221. DOI : 10.1021/acs.joc.6b01166
https://https://hal.archives-ouvertes.fr/hal-03229299v1

Gold-catalyzed rearrangement of (silylcyclopropenyl)methyl ethers into (silylmethylene)cyclopropanes
F. Hiault, A. Archambeau, F. Miege, C. Meyer, J. Cossy
Synthesis 2016, 48, 3165-3174. DOI : 10.1055/s-0035-1561486
https://https://hal.archives-ouvertes.fr/hal-03229300v1

Total synthesis of putative 11-epi-lyngbouilloside aglycon
A. Kolleth, J. Gebauer, A. ElMarrouni, R. Lebeuf, C. Prévost, E. Brohan, S. Arseniyadis, J. Cossy
Front. Chem, Vol 4, Article number 34, August 2016. DOI : 10.3389/fchem.2016.00034
https://https://hal.archives-ouvertes.fr/hal-03229302v1

Expanding Biohybrid-mediated Asymmetric Catalysis into the Realm of RNA.
N. Duchemin, E. Benedetti, L. Bethge, S. Vonhoff, S. Klussmann, J.-J. Vasseur, J. Cossy, M. Smietana, S. Arseniyadis
Chem. Commun. 2016, 52, 8604-8607. DOI : 10.1039/C6CC03540J
https://https://hal.archives-ouvertes.fr/hal-02197262v1

Natural Products Containing Oxygen Heterocycles—Synthetic Advances Between 1990 and 2015
J. Cossy, A. Guérinot
Advances in Heterocyclic Chemistry, 2016 119, 107-142. DOI : 10.1016/bs.aihch.2016.03.002
https://https://hal.archives-ouvertes.fr/hal-03229303v1

Harnessing C–H activation of benzhydroxamates as a macrocyclization strategy : synthesis of structurally diverse macrocyclic isoquinolones
J.-P. Krieger, G. Ricci, D. Lesuisse, C. Meyer, J. Cossy
Chem. Eur. J. 2016, 22, 13469-13473. DOI : 10.1002/chem.201602332
https://https://hal.archives-ouvertes.fr/hal-03229304v1

Rhodium(II)-catalyzed isomerization of cyclopropenylmethyl esters into (acyloxymethylene)cyclopropanes
A. Archambeau, D.-V. Nguyen, C. Meyer, J. Cossy
Chem. Eur. J. 2016, 22, 6100-6110. DOI : 10.1002/chem.201505063
https://https://hal.archives-ouvertes.fr/hal-03229305v1

Design, synthesis and binding affinity evaluation of Hoechst 33258 derivatives for the development of sequence-specific DNA-based asymmetric catalysts
K. Amirbekyan, N. Duchemin, E. Benedetti, R. Joseph, A. Colon, S. A. Markarian, L. Bethge, S. Vonhoff, S. Klussmann, J. Cossy, J.-J. Vasseur, S. Arseniyadis, M. Smietana
ACS Catal. 2016, 6, 3096-3105. DOI : 10.1021/acscatal.6b00495
https://https://hal.archives-ouvertes.fr/hal-02197253v1