A. Studer, D. P. Curran, T. Mccallum, L. Barriault, P. Nuhant et al., Par souci de simplification, nous ferons référence sous le terme « photocatalyse » à toutes les réactions chimiques où la lumière est impliquée. Pour plus d'informations sur la photocatalyse en chimie radicalaire, vol.55, pp.3487-3490, 2016.

D. H. Barton, B. Garcia, H. Togo, and S. Z. Zard, Tetrahedron Lett, vol.27, pp.1327-1330, 1986.

H. Togo, K. Hayashi, and M. Yokoyama, Chem. Lett, vol.22, pp.641-644, 1993.

B. Quiclet-sire, S. Zard, and . Synlett, Des études préliminaires ont des résultats encourageants lors de la formation du 3-phtalimidopyrrole correspondant : Cheibas, C.; Revil-Baudard, vol.28, pp.2685-2696, 2017.

L. Fu, G. Gribble, D. Korakas, G. J. Varvounis, . Heterocycl et al., Pour quelques exemples d'accès aux dérivés de 3-aminopyrroles, vol.33, pp.4485-4494, 1990.

K. J. Morgan and D. P. Morrey, Tetrahedron, vol.22, pp.57-62, 1966.

T. Ly, B. Quiclet-sire, B. Sortais, S. Z. Zard, T. L. Harris et al., Bioorg. Med. Chem. Lett, vol.40, pp.4516-4519, 1999.

L. Debien and S. Z. Zard, J. Am. Chem. Soc, vol.135, pp.3808-3811, 2013.

F. Tonsiengsom, F. Y. Miyake, K. Yakushijin, and D. A. Horne, Synthesis, issue.1, 2006.

, 2 g, 50 mmol, 1 equiv) and water (50 mL) were added Adogen ® 464 (1.7 g) and potassium Oethyl xanthate (8 g, 50 mmol, 1 equiv). The resulting biphasic mixture was vigorously stirred for 1.5 h at 23 °C before extracting the desired xanthate with PE. The yellow solution was then concentrated down and filtered through a pad of SiO2 using PE as eluent to afford xanthate VI

, Methylquinolin-2-yl)butane-1,4-diyl)bis(isoindoline-1,3-dione) VI, vol.2, p.21

, 71 mg, 0.5 mmol, 1.0 equiv) in 1,2-dichloroethane (1 mL) was reacted with xanthate VI.20 (117 mg, 1.0 mmol, 2.0 equiv), in the presence of camphorsulfonic acid (116 mg, 0.5 mmol, 1.0 equiv) and DLP (600 mg, 1.5 mmol, 3.0 equiv). Work-up was carried out according to Work-up Procedure 1 and the obtained residue was purified by flash chromatography

, Methylquinolin-2-yl)cyclobutyl acetate VII

, mL) was reacted with xanthate VII.1 (234 mg, 1.0 mmol, 2.0 equiv), in the presence of camphorsulfonic acid (116 mg, 0.5 mmol, 1.0 equiv) and DLP (600 mg, 1.5 mmol, 3.0 equiv). Work-up was carried out according to Work-up Procedure 1 and the obtained residue was purified by flash chromatography (SiO2; PE/Toluene/EtOAc 85:10:5) to give compound VII.11 (64 mg, 50%) as a brown solid, mg, 0.5 mmol, 1.0 equiv, vol.1, p.2