Enantioselective synthesis of tetra-substituted tetralines and tetrahydro-indolizines by NHC-catalyzed azolium–enolate cascade

Ghosh, Arghya ; Barik, Shilpa ; Shee, Sayan ; Biju, Akkattu T. (2021) Enantioselective synthesis of tetra-substituted tetralines and tetrahydro-indolizines by NHC-catalyzed azolium–enolate cascade Chemical Communications, 57 (63). pp. 7794-7797. ISSN 1359-7345

Full text not available from this repository.

Official URL: http://doi.org/10.1039/D1CC03165A

Related URL: http://dx.doi.org/10.1039/D1CC03165A

Abstract

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.

Item Type:Article
Source:Copyright of this article belongs to Royal Society of Chemistry
ID Code:128584
Deposited On:03 Nov 2022 06:37
Last Modified:03 Nov 2022 06:37

Repository Staff Only: item control page