Categories: Synthesis of N-Heterocycles >
Synthesis of indolizinones
Recent Literature

A copper-catalyzed cycloisomerization of 2-pyridyl-substituted propargylic
acetates and its derivatives offers an efficient route to C-1 oxygenated
indolizines with a wide range of substituents under mild reaction conditions.
The presented method could be readily applied to the synthesis of indolizinones
through a cyclization/1,2-migration of tertiary propargylic alcohols.
B. Yan, Y. Zhou, H. Zhang, J. Chen, Y. Liu, J. Org. Chem.,
2007,
72, 7783-7786.
