1, 3-Dipolar cycloaddition reactions are fundamental processes in organic chemistry, 1 and
their asymmetric version offers a powerful and reliable synthetic methodology to access five …

Heterocyclic synthesis involving transition metal complexes has become of common use in
the past decade because a transition-metal-catalyzed reaction can directly build …

This review will attempt to cover the literatures published from 1988 dealing with cyclic and
acyclic azomethine ylides in which a part or the whole of the ylide conjugation is included in …

We report a new catalyst system that should enhance the use of enantioselective 1, 3-
dipolar cycloadditions of azomethine ylides with electronic-deficient olefins in the divergent …

Pyrrolidines, the 5 membered aza-heterocycles, substituted at the 2 and 5 positions, are very
often encountered in the living organisms. Since the 1970's where the first pyrrolidinic …

Several [3+ 2] thermal cycloadditions between azomethine ylides and nitroalkenes have
been studied both theoretically and experimentally. When the N-metalated 1, 3-dipoles are …

The [3+ 2] cycloaddition reaction between several N-metalated azomethine ylides and
nitroalkenes has been studied using AgOAc and LiClO4 as metalating reagents in the …

A novel anti-HIV alkaloid, drymaritin (1), and a new C-glycoside flavonoid, diandraflavone
(2), along with eight known compounds, torosaflavone A, isovitexin, spinasterol β-d …

Silver fluoride and cinchona alkaloids catalyze the diastereo-and enantioselective 1, 3-
dipolar cycloaddition between azomethine ylides, generated from N-alkylideneglycine …

We expand upon recent results concerning dipolar cycloaddition reactions of unstabilized
azomethine ylids with nitro alkenes to generate 3-nitropyrrolidines via a flow chemistry …