
Tetrahedron (2021)
Update date:2022-08-04
Topics:
Barlow, Sean R.
Callaghan, Lily J.
Franckevi?ius, Vilius
The palladium-catalysed cyclisation of propargylic electrophiles with nucleophiles represents a useful synthetic approach for the rapid construction of heterocyclic building blocks. However, these cyclisation reaction processes often pose a number of challenges due to the need for the simultaneous control of chemo-, regio- and stereoselectivity. Herein, we disclose the discovery of α-amido malonates as novel bis-nucleophiles in the highly chemo- and regioselective, as well as moderately enantioselective, palladium-catalysed cyclisation with propargylic compounds to afford a broad range of functionalised dihydrooxazine heterocycles. The new dihydrooxazine products will expand the suite of heterocycles available to medicinal chemists, and prompt the investigation of unchartered bis-nucloeophiles in palladium-catalysed cyclisation reactions en route to novel classes of heterocycle.
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Doi:10.1021/ja01100a507
(1953)Doi:10.1021/ja01206a051
(1946)Doi:10.1016/j.mcat.2018.06.003
(2018)Doi:10.1007/BF00923228
()Doi:10.1021/ja00827a046
(1974)Doi:10.1248/cpb.25.79
(1977)