116726-73-9Relevant academic research and scientific papers
Iron-catalyzed ring-opening of meso-aziridines with amines
Marti, Alex,Richter, Luise,Schneider, Christoph
, p. 2513 - 2516 (2011)
A cationic iron complex has been found to catalyze the aminolysis of meso-N-aryl aziridines very efficiently furnishing valuable 1,2-diamines in typically excellent yields. This protocol is compatible with a range of functional groups both in the aziridine and amine components. Georg Thieme Verlag Stuttgart · New York.
The Ti-BINOLate-catalyzed, enantioselective ring-opening of meso-aziridines with amines
Peruncheralathan, Saravanan,Aurich, Sandra,Teller, Henrik,Schneider, Christoph
, p. 2787 - 2803 (2013/05/08)
The titanium-BINOLate-catalyzed, highly enantioselective ring-opening reaction of meso-aziridines has been developed which furnishes trans-1,2-diamines in typically good yields and excellent enantioselectivities. N-Aryl aziridines attached to a 5- or 6-me
Mild and efficient method for regioselective ring opening of aziridines with amines by bismuth trichloride
Swamy, Navath Raghavendra,Venkateswarlu
, p. 547 - 554 (2007/10/03)
Aziridines undergo the facile ring opening with anilines to afford the 1,2-diamines in excellent yields by bismuth trichloride in acetonitrile at ambient temperature.
Silica gel induced cleavage of aziridines by aromatic amines under solvent free conditions
Anand, R. Vijaya,Pandey, Ghanshyam,Singh, Vinod K.
, p. 3975 - 3976 (2007/10/03)
A variety of aziridines were opened in an efficient manner with aromatic amines using silica gel under solvent free conditions.
