This review provides the authors' selection of recent publications that highlight the
increasing efforts to develop valuable organocatalytic domino/tandem/cascade reactions as …

Aza‐ortho‐quinone methides allow the straightforward asymmetric synthesis of natural‐
product‐inspired indole scaffolds possessing a quaternary stereocenter. Our approach …

Many nitrogen-moiety containing alkaloids derived from plant origins are bioactive and play
a significant role in human health and emerging medicine. Noscapine, a …

Biology‐oriented synthesis employs the structural information encoded in complex natural
products to guide the synthesis of compound collections enriched in bioactivity. The trans …

The limited structural diversity that a compound library represents severely restrains the
discovery of bioactive small molecules for medicinal chemistry and chemical biology …

In an endeavor to provide an efficient route to natural product hybrids, described herein is an
efficient, highly stereoselective, one‐pot process comprising an organocatalytic conjugate …

Abstract Enantioselective catalytic intermolecular 1, 3‐dipolar cycloadditions are powerful
methods for the synthesis of heterocycles. In contrast, intramolecular enantioselective 1, 3 …

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Aza‐ortho‐Chinonmethide ermöglichen eine effiziente asymmetrische Synthese Naturstoff‐
inspirierter Indolgerüste mit quartärem Stereozentrum. Mit diesem Ansatz konnten diverse …

A catalytic two-step reaction sequence was developed to access a range of complex
heterocyclic frameworks based on biorelevant indole/oxindole scaffolds. The reaction …