Highly Enantioselective Ring-Opening Reactions of Aziridines with Indole and 19- 048 Its Application in the Building of C3-Halogenated Pyrroloindolines. — A magne- sium-catalyzed asymmetric ring-opening reaction of aziridine with indole is realized by employing commercially available chiral ligands. The ring-opening product can be further transformed to various types of enantioenriched C3-halogenated-pyrrolo- indolines. — (YANG, D.; WANG, L.; HAN, F.; LI, D.; ZHAO, D.; CAO, Y.; MA, Y.; KONG, W.; SUN, Q.; WANG*, R.; Chem. - Eur. J. 20 (2014) 50, 16478-16483, http://dx.doi.org/10.1002/chem.201404354 ; Sch. Life Sci., Lanzhou Univ., Lanzhou, Gansu 730000, Peop. Rep. China; Eng.) — U. Scheffler