Reductive amination plays a paramount role in pharmaceutical and medicinal chemistry
owing to its synthetic merits and the ubiquitous presence of amines among biologically …

An organocatalyzed asymmetric Michael addition reaction has been established as the most
relevant and dynamic research area for the construction of chiral carbon‐carbon and carbon …

Enantioselective α‐branched aldehyde Michael addition to N‐phenylmaleimide resulting in
non‐stereogenic quaternary carbon containing succinimides is common. Here we …

The acid–base pairing and fabrication method was herein employed to construct acid–base
bifunctional heterogeneous catalysts. The boronic acid group was introduced into primary …

Abstract Asymmetric organocatalytic 1, 4‐conjugate addition is considered as an effective,
powerful and sustainable method for carbon‐carbon bond formation. The core structure of …

A rapid pathway for the synthesis of various β-phenethylamines from aromatic aldehydes
has been developed. Initially, a wide range of 5-aryloxazolidines was prepared via the [3+ 2] …

Asymmetric Michael additions of isobutyraldehyde to maleimides catalyzed by optically pure
diamines and their sulfonamides were investigated to develop heterogeneous chiral …

We describe the development of the catalytic reductive alkylation of amines with aldehydes
under the atmospheric pressure of H2 using a brush-like silicon-nanostructure-supported …

An organocatalytic asymmetric cascade Michael/hemiketalization/acyl transfer reaction
between (E)-2-(2-nitrovinyl) phenols and 1, 3-propanediones is disclosed. A cinchona …

Synthesis of the diarylindolizidine alkaloid (+)-Fistulopsine B: Application of an organocatalytic
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