Indolizidine alkaloids are chemical constituents isolated from various marine and terrestrial
plants and animals, including but not limited to trees, fungi, ants, and frogs, with a myriad of …

This paper provides a review on various methodologies developed for the synthesis of
different indolizine derivatives and an overview of their application. These include …

Simultaneous deconstructive ring-opening and skeletal reconstruction of an inert, aromatic
pyridinium ring is of great importance in synthetic communities. However, research in this …

Herein we report the synthesis of substituted indolizidines and related N-fused bicycles from
simple saturated cyclic amines through sequential C–H and C–C bond functionalizations …

Saturated N‐heterocycles are prominent motifs found in various natural products and
pharmaceuticals. Despite the increasing interest in this class of compounds, the synthesis of …

Acid-catalyzed intramolecular cyclization or rearrangement of isoindolinone derivatives is
described. 3-Hydroxy/ethoxy-3, 4-dihydro-6H-[1, 4]-oxazino-[3, 4-a]-isoindol-6-ones are …

An aza-Robinson annulation strategy is described using a NaOEt-catalyzed conjugate
addition of cyclic imides onto vinyl ketones, followed by a TfOH-mediated intramolecular …

Cyclization strategies employing imides and their derivatives have attracted the attention of
several organic chemists interested in synthesizing polycyclic alkaloids. Numerous …

The enantioselective synthesis of isoindolones via Heck‐Mizoroki reactions of endocyclic
enamides using a palladium‐bis (oxazoline) catalyst system is described. The N, N‐ligands …

The nitrogen-bridgehead is a common structural motif present in a multitude of natural
products. As many of these abundant compounds exhibit biological activities, eg against …