The chemistry, synthetic routes and medicinal properties of vicinal diamines and
imidazolines are discussed. Synthetic routes towards chemically and pharmaceutically …

Chemistry based on ring opening of aziridines has been widely studied in organic synthesis.
However, it has mainly been centered on ring opening by nucleophiles and on cycloaddition …

Herein we report a nickel-catalyzed regioselective cross-electrophile ring opening reaction
of sulfonyl-protected aziridines with trifluoromethyl-substituted alkenes as the gem …

A transition metal-free, atom-economical, and highly stereospecific synthetic approach to
Friedel–Crafts-type alkylation of arenes/heteroarenes has been developed. The protocol …

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 …

Alkyl and aryl isothiocyanates and carbodiimides are effective substrates in (3+ 2)
cycloadditions with N‐sulfonyl‐2‐substituted aziridines and 2‐phenylaziridine for the …

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 …

This account highlights the most relevant transformations of cycloalkane-fused oxiranes and
aziridines developed during the past decade with the intention to provide an overview of the …

AgSbF6-Promoted Cycloaddition Reaction of 2-Trifluoromethyl-N-tosylaziridine with
Aldehydes | Organic Letters ACS ACS Publications C&EN CAS Find my institution Log In …