1415033-58-7Relevant academic research and scientific papers
Enantioselective synthesis of tetra-substituted tetralines and tetrahydro-indolizines by NHC-catalyzed azolium-enolate cascade
Barik, Shilpa,Biju, Akkattu T.,Ghosh, Arghya,Shee, Sayan
supporting information, p. 7794 - 7797 (2021/08/13)
NHC-catalyzed cascade reaction of enals with suitably substituted β-(hetero)aryl enones allowing the enantioselective synthesis of tetra-substituted tetralines and tetrahydro indolizines is presented. The catalytically generated chiral α,β-unsaturated acylazoliums from enals under oxidative conditions reacted in a Michael-Michael-lactonization sequence to form the tricyclic δ-lactone products bearing four contiguous stereocentres.
NHC Bronsted base-catalyzed transformations of isochromene derivatives: Regulation of products by the structures of carbene catalysts
Fan, Xing-Wen,Cheng, Ying
, p. 9079 - 9084,6 (2020/10/15)
Two different transformations of α-(isochromen-1-yl)ketones catalyzed by NHC Bronsted bases are reported. In the presence of a triazole carbene, α-(isochromen-1-yl)ketones isomerized into β-(2-(aroylmethylene) phenyl)-α,β-unsaturated ketones in 38-88% yields, while the same reaction catalyzed by an imidazole carbene produced 1-aroylnaphthalene derivatives in 90-99% yields. This work not only provides a new method for the synthesis of a novel type of α,β-unsaturated ketone and multi-substituted naphthalene derivatives, but also advances the application of NHC catalysts in the field of Bronsted base-catalysis.
