Developments in the synthesis of indolizines during the last decade are reviewed, with special emphasis given to strategies relying on pyrrole derivatives and on π-expanded systems.
This review summarizes recent advances in electrochemical and photocatalytic C–H functionalization of indolizines, with an emphasis on the construction of C–C and C–X (X = S, Se, N, Cl, Br, etc.) bonds.
Cancer remains a major global health challenge and a leading cause of mortality. This ongoing burden underscores the need for continuous exploration of novel therapeutic strategies, prompting extensive review of emerging targets, mechanisms, and treatment approaches.
A sustainable electrochemical approach for site-selective C–H mono and bis-chalcogenation (sulfenylation or selenylation) of indolizine frameworks is described.
Tricyclic indolizines can be obtained in water in one step by a Morita–Baylis–Hillman/aza-Michael cyclization/dehydration cascade.