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Cite the Following Article
Et3B-mediated and palladium-catalyzed direct allylation of β-dicarbonyl compounds with Morita–Baylis–Hillman alcohols
Ahlem Abidi, Yosra Oueslati and Farhat Rezgui
Beilstein J. Org. Chem. 2016, 12, 2402–2409.
https://doi.org/10.3762/bjoc.12.234
How to Cite
Abidi, A.; Oueslati, Y.; Rezgui, F. Beilstein J. Org. Chem. 2016, 12, 2402–2409. doi:10.3762/bjoc.12.234
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Scholarly Works
- Mhasni, O.; Elleuch, H.; Rezgui, F. Direct nucleophilic substitutions of allylic alcohols with 1,3-dicarbonyl compounds: Synthetic design, mechanistic aspects and applications. Tetrahedron 2022, 111, 132732. doi:10.1016/j.tet.2022.132732
- Nagae, H.; Xia, J.; Kirillov, E.; Higashida, K.; Shoji, K.; Boiteau, V.; Zhang, W.; Carpentier, J.-F.; Mashima, K. Asymmetric Allylic Alkylation of β-Ketoesters via C–N Bond Cleavage of N-Allyl-N-methylaniline Derivatives Catalyzed by a Nickel–Diphosphine System. ACS Catalysis 2020, 10, 5828–5839. doi:10.1021/acscatal.0c01356
- Omrani, A.; Rezgui, F.; Duñach, E.; Poulain-Martini, S. Bi(OTf)3-catalysed regioselective arylation of Morita-Baylis-Hillman type allylic electrophiles. Tetrahedron Letters 2020, 61, 151758. doi:10.1016/j.tetlet.2020.151758
