·. Ch, ), LCMS (EI, pp.9-11

H. Nmrm, 3. , and 2. , CDCl 3 ): d = 7, MHz CH arom CH arom, vol.15733, issue.701, p.47

7. , 2. , and J. Hh-=-9-hz, CDCl 3 ): d = 715 (s, 3H, N?CH 3 ), HH = 12 Hz J HH = 2.7 Hz, pp.218-223

H. Nmrm, 3. , and 3. , CDCl 3 ): d = 7, MHz CH arom CH arom, vol.158, issue.7, p.472712

2. and J. Hh, 15 (s, 3H, N?CH 3 ); 13 C NMR (75 MHz, CDCl 3 ): d = 167, C@OCqCqCqCH arom, vol.3277, issue.1329, pp.2-2

A. Klapars, J. C. Antilla, X. Huan, S. L. Buchwald, and A. Klapars, -Arylation of Nitrogen Heterocycles, Journal of the American Chemical Society, vol.123, issue.31, pp.7727-7729, 2001.
DOI : 10.1021/ja016226z

A. Klapars and S. L. Buchwald, Copper-Catalyzed Halogen Exchange in Aryl Halides:?? An Aromatic Finkelstein Reaction, Journal of the American Chemical Society, vol.124, issue.50, pp.14844-14845, 2002.
DOI : 10.1021/ja028865v

P. Toto, J. Gesquière, B. Deprez, and N. Willand, Synthesis of N-(iodophenyl)-amides via an unprecedented Ullmann???Finkelstein tandem reaction, Tetrahedron Letters, vol.47, issue.7, pp.1181-1186, 2006.
DOI : 10.1016/j.tetlet.2005.12.022
URL : https://hal.archives-ouvertes.fr/inserm-00110438

A. Vigroux, M. Bergon, C. Bergonzi, and P. Tisnes, A General Acid-Catalyzed Anion Breakdown Associated with an E1cB Reaction in the Hydrolysis of Aryl N-(Substituted Phenylsulfonyl)carbamates, Journal of the American Chemical Society, vol.116, issue.26, pp.11787-11796, 1994.
DOI : 10.1021/ja00105a020

F. G. Bordwell and G. Z. Ji, Effects of structural changes on acidities and homolytic bond dissociation energies of the hydrogen-nitrogen bonds in amidines, carboxamides, and thiocarboxamides, Journal of the American Chemical Society, vol.113, issue.22, pp.8398-8401, 1991.
DOI : 10.1021/ja00022a029

F. G. Bordwell and H. G. Fried, Heterocyclic aromatic anions with 4n + 2 .pi.-electrons, The Journal of Organic Chemistry, vol.56, issue.13, pp.4218-4223, 1991.
DOI : 10.1021/jo00013a027

A. V. Willi, Die Acidit??tskonstanten von Benzolsulfonamiden und ihre Beeinflussbarkeit durch Substitution, Helvetica Chimica Acta, vol.77, issue.1, pp.46-48, 1956.
DOI : 10.1002/hlca.19560390106