In the past decade, the asymmetric synthesis of chiral nonracemic isoquinoline alkaloids, a
family of natural products showing a wide range of structural diversity and biological and …

Phenylglycinol‐derived oxazolopiperidone lactams are exceptionally versatile building
blocks for the enantioselective construction of structurally diverse piperidine‐containing …

The intramolecular α‐amidoalkylation reactions of aromatic and heteroaromatic ring systems
constitute a versatile approach for the synthesis of nitrogen heterocyles in a …

A diverse stereodivergent organocatalytic one‐pot addition/cyclization/annulation sequence
to optically active quinolizidine derivatives from easily available starting materials is …

Here we present a general and common catalytic asymmetric strategy for the total and
formal synthesis of a broad number of optically active natural products from the …

An expedient diastereoselective synthesis of highly functionalized indolo [2, 3-α]
quinolizidines adopting a cis H2/H12b geometry has been realized by a Pictet− Spengler …

An enantioselective two-step route to substituted benzo [a]-and indolo [2, 3-a] quinolizidines
has been developed. It consists of (i) a stereoselective cyclocondensation of a racemic or …

An asymmetric organocatalyzed reaction sequence involving a Michael addition of various
1, 3‐dicarbonyl compounds to α, β‐unsaturated aldehydes with subsequent …

An enantiospecific and stereoselective total synthesis of the natural product (+)-crispine A
has been demonstrated employing a Pictet− Spengler bis-cyclization reaction between …

A highly efficient enantioselective enamine-catalyzed asymmetric conjugate addition has
been developed to directly convert unfunctionalized cyclic α-hydroxyamides into chiral cyclic …