30303-39-0Relevant academic research and scientific papers
Silica gel induced cleavage of aziridines by aromatic amines under solvent free conditions
Anand, R. Vijaya,Pandey, Ghanshyam,Singh, Vinod K.
, p. 3975 - 3976 (2002)
A variety of aziridines were opened in an efficient manner with aromatic amines using silica gel under solvent free conditions.
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
Iron-catalyzed ring-opening of meso-aziridines with amines
Marti, Alex,Richter, Luise,Schneider, Christoph
experimental part, p. 2513 - 2516 (2011/11/13)
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.
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.
