Indolizine (pyrrolo [1, 2-a] pyridine) is one of the five isomers of indole and it serves as a
precursor for widespread indolizidine alkaloids. The straightforward synthesis of indolizines …

This review is intended to highlight the most useful approaches for the synthesis of indole
derivatives (azaindoles, carbazoles, carbolines, indazoles, 3H‐indoles, indolines …

Conversion of Pyridine to Imidazo[1,2-a]pyridines by Copper-Catalyzed Aerobic
Dehydrogenative Cyclization with Oxime Esters | Organic Letters ACS ACS Publications C&EN …

Here, an environmentally benign electrooxidative approach to the intramolecular
aminooxygenation of alkynes has been developed. The method allows for the rapid …

A highly efficient [4+ 2] annulation route to polysubstituted indolizines is described
employing a domino Knoevenagel condensation/intramolecular aldol cyclization process as …

Fluorescence-based technologies play a pivotal role in various biomedical applications.
Here we report an efficient route to a new class of fluorophores, indolizino [3, 2-c] quinolines …

A new synthetic route to indolizines with various substituents on the pyridine moiety was
developed by utilizing a facile cycloaromatization of 2-acetylpyrrole derivatives. Without …

An efficient method for the synthesis of new indolizine-fused chromones has been
accomplished from ethyl (E)-3-(2-acetylphenoxy) acrylates and pyridines in a “one-pot” …

In this study, we describe the hydrogenation of indolizines derived from Morita–Baylis–
Hillman adducts. We demonstrate that functionalized tetrahydroindolizines and indolizidines …

Diversity-oriented construction of new indolizine scaffolds was accomplished by utilizing
domino Knoevenagel condensation/intramolecular aldol cyclization. Biological evaluation …