In this critical review, the ring opening of non-activated 2-substituted aziridinesvia
intermediate aziridinium salts will be dealt with. Emphasis will be put on the relationship …

Environmentally friendly hypervalent iodine reagents are unusually effective promoters of
asymmetric α-functionalization of carbonyl compounds. By using hypervalent iodine …

Developing olefin isomerization reactions to reach kinetically controlled Z-alkenes is
challenging because formation of trans-alkenes is thermodynamically favored under the …

Three kinds of porous organic polymers (POPs) containing N or P atoms were prepared,
named N-POP, P-POP, and N+ P-POP respectively and used as the supports for Rh …

The asymmetric formal hydroamination of enamines using a CuH catalyst is reported. The
method provides a straightforward and efficient approach to the synthesis of chiral 1, 2 …

Sialylconjugates on cell surfaces are involved in many biological events such as cellular
recognition, signal transduction, and immune response. It has been reported that aberrant …

The concept of pharmacophore hybridization is attracting an increasing interest from
medicinal chemists. Whereas the main motivation for the application of this methodology …

Chiral aziridine‐2‐carboxylates have two important functional groups, the carboxylate group
and aziridine ring, that are useful for synthetic purposes. As both (2R)‐and (2S)‐aziridine‐2 …

Ring opening of 1-arylmethyl-2-(cyanomethyl) aziridines with HBr afforded 3-(arylmethyl)
amino-4-bromobutyronitriles via regiospecific ring opening at the unsubstituted aziridine …

The ring‐opening reactions of 2‐alkyl‐substituted 1, 1‐bis (arylmethyl)‐and 1‐methyl‐1‐(1‐
phenylethyl) aziridinium salts with fluoride, chloride, bromide and iodide in acetonitrile have …