Copper-Catalyzed Asymmetric Propargylation of Indolizines

01 natural sciences 0104 chemical sciences
DOI: 10.1021/acs.orglett.9b03032 Publication Date: 2019-10-23T18:29:01Z
ABSTRACT
Methods to diversify indolizines are valuable for the discovery of medications and fluorescent molecules. The utilization of copper-catalyzed asymmetric propargylation to install a terminal alkyne handle on indolizine heterocycle is reported. This method delivers C3-propargylation products from C2-substituted indolizines or C1-propargylation products from C2,C3-disubstituted indolizines through a stereoconvergent pathway.
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