Catalytic aziridination of alkenes with nitrene sources via “C2+ N1” addition represents a
general approach for the direct synthesis of aziridines, the smallest three-membered N …

A highly regioselective Lewis acid-mediated SN2-type ring-opening of N-sulfonylaziridines
and azetidines with tetraalkylammonium halides in CH2Cl2 solution to afford 1, 2-and 1, 3 …

An imidazole-based zwitterionic-salt, 4-(3-methylimidazolium) butane sulfonate (MBS), has
been found to be an efficient organocatalyst for aziridine ring-opening regioselectively by …

Lewis acid catalyzed quaternary ammonium salt mediated highly regioselective ring-
opening of chiral activated aziridines and azetidines with alcohols to nonracemic β-and γ …

A highly enantio-and diastereoselective Lewis acid catalyzed SN2-type ring opening
followed by cyclization of aziridines with active methylene carbon nucleophiles to …

A highly regio-and stereoselective strategy for the syntheses in high yield and
enantioselectivity of a variety of substituted nonracemic morpholines and their homologues …

A highly regio-and stereoselective route for the synthesis of racemic and nonracemic
tetrahydroquinoxalines via the SN2-type ring-opening of activated aziridines with 2 …

A series of novel sulfonamide azoles were synthesized via C–N cleavage of sulfonamides
by an azole ring. This type of reaction could be performed smoothly in DMF and some …

A simple strategy for the synthesis of substituted tetrahydroquinolines through regio-and
stereoselective ring opening of N-tosyl aziridines with carbon nucleophiles generated from 2 …

Abstract The BF3⋅ OEt2‐catalyzed reaction of azulene with N‐protected aziridines
represents a general, efficient (up to 91% yield) and regioselective approach to …