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Journal ArticleDOI

Carbene-Catalyzed Activation of Formyl-phenylacetic Esters for Access to Chiral Dihydroisoquinolinones.

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TLDR
In this article, a carbene-catalyzed reaction to synthesize chiral dihydroisoquinolinones via an o-quinodimethane (o-QDM) intermediate is disclosed.
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This article is published in Organic Letters.The article was published on 2021-09-17. It has received 3 citations till now. The article focuses on the topics: Annulation & Acylation.

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NHC‐catalyzed 1,4‐elimination in the dearomative activation of 3‐furaldehydes towards (4+2)‐cycloadditions

TL;DR: In this paper , a (4+2)-cycloaddition reaction between 2-substituted 3-furaldehydes derivatives and isatins or α,α,α-trifluoroacetophenones as electrophiles has been established under NHC-catalysis.
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NHC-catalyzed N-H functionalization/cycloaddition reaction of indole aldehyde and ketone: A DFT perspective

TL;DR: In this paper , the authors theoretically investigated the mechanism and origin of stereoselectivity in N-heterocyclic carbene (NHC)-catalyzed NH functionalization/cycloaddition reaction of indole aldehyde and ketone.
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NHC‐Activations on α‐, β‐, γ‐, and Beyond

TL;DR: In this article , the authors focus on the development of NHC activation of carbonyl carbon (or imine carbon) in situ, α−, β−, γ−, and beyond, and the cycloaddition reaction of these species.
References
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Journal ArticleDOI

Carbene-Catalyzed Enantioselective Decarboxylative Annulations to Access Dihydrobenzoxazinones and Quinolones.

TL;DR: Complementary dispersion-corrected density functional theory (DFT) studies provided an accurate prediction of the reaction enantioselectivity and lend further insight to the origins of stereocontrol.
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Hit-to-lead studies for the antimalarial tetrahydroisoquinolone carboxanilides.

TL;DR: Phenotypic whole-cell screening in erythrocytic cocultures of Plasmodium falciparum identified a series of dihydroisoquinolones that possessed potent antimalarial activity against multiple resistant strains of P. falcIParum in vitro and show no cytotoxicity to mammalian cells in vivo.
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Addition of N-Heterocyclic Carbene Catalyst to Aryl Esters Induces Remote C-Si Bond Activation and Benzylic Carbon Functionalization.

TL;DR: Through the incorporation of a silicon atom to an aryl carboxylic ester substrate, the resulting C-Si bond can be activated via the addition of a carbene catalyst on a remote site, which allows for efficient functionalization of the benzylic sp3-carbons of aryL carboxYlic esters.