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
AUTHORS (5)
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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