Themed collection Organic Chemistry Frontiers Emerging Investigator Series 2024–2025

15 items
Research Article

Synthesis of antimicrobial active 9,10-phenanthrenequinones by carbene organocatalytic tandem reactions

An N-heterocyclic carbene organocatalytic approach that enables the rapid construction of a diverse range of PQs has been disclosed.

Graphical abstract: Synthesis of antimicrobial active 9,10-phenanthrenequinones by carbene organocatalytic tandem reactions
Research Article

Access to (bridged) bicyclic ureas through azocarboxamide-enabled enantioselective 1,2-diamination of α-branched cyclic ketones

Reported here is the azocarboxamide-enabled enantioselective 1,2-diamination of α-branched cyclic ketones. A wide range of fused and bridged bicyclic ureas were prepared in good yield with excellent enantioselectivity.

Graphical abstract: Access to (bridged) bicyclic ureas through azocarboxamide-enabled enantioselective 1,2-diamination of α-branched cyclic ketones
Open Access Research Article

Access to fluorinated dienes through hydrofluorination of 2-En-4-ynoates

The hydrofluorination of enynoates has been developed for the synthesis of fluorinated dienoates.

Graphical abstract: Access to fluorinated dienes through hydrofluorination of 2-En-4-ynoates
Research Article

Diverse enantioselective synthesis of hetero[7]helicenes via an organocatalyzed double annulation strategy

A versatile method has been devised for the catalytic enantioselective synthesis of hetero[7]helicenes utilizing organocatalyzed double annulation and aromatization.

Graphical abstract: Diverse enantioselective synthesis of hetero[7]helicenes via an organocatalyzed double annulation strategy
Research Article

Stereocontrolled desymmetrization of 2,5-cyclohexadienones via organocatalytic domino sulfa-1,6-/1,4-addition or sulfa-1,6-/1,4-/sulfa-1,4-addition reactions

A squaramide-catalyzed regio-/enantioselective sulfa-1,6-addition initiated highly enantio- and diastereoselective desymmetrization of 2,5-cyclohexadienone-tethered 3-cyano-4-styrylcoumarins has been disclosed.

Graphical abstract: Stereocontrolled desymmetrization of 2,5-cyclohexadienones via organocatalytic domino sulfa-1,6-/1,4-addition or sulfa-1,6-/1,4-/sulfa-1,4-addition reactions
Research Article

Cobalt-catalyzed stereoselective synthesis of chiral gem-difluorocyclopropanes with vicinal stereocenters

We present a cobalt-catalyzed regio-, diastereo-, and enantioselective hydroalkylation of gem-difluorocyclopropenes, accessing chiral gem-difluorocyclopropanes with vicinal stereocenters.

Graphical abstract: Cobalt-catalyzed stereoselective synthesis of chiral gem-difluorocyclopropanes with vicinal stereocenters
From the themed collection: 2024 Organic Chemistry Frontiers HOT articles
Research Article

Cobalt-catalyzed enantioselective reductive addition of ketimine with cyclopropyl chloride to construct chiral amino esters bearing cyclopropyl fragments

Co-catalyzed asymmetric reductive addition of ketimine with cyclopropyl chloride has been realized to access diverse chiral amino esters bearing cyclopropyl fragments with broad functional group tolerance and excellent enantioselectivities.

Graphical abstract: Cobalt-catalyzed enantioselective reductive addition of ketimine with cyclopropyl chloride to construct chiral amino esters bearing cyclopropyl fragments
From the themed collection: 2024 Organic Chemistry Frontiers HOT articles
Open Access Research Article

Well-defined chiral dinuclear copper-catalyzed tandem asymmetric propargylic amination–carboxylative cyclization sequence toward chiral 2-oxazolidinone derivatives

A variety of chiral 2-oxazolidinones was obtained via a dinuclear copper-catalyzed asymmetric propargylic amination–carboxylative cyclization sequence of propargylic esters with alkyl amine hydrochlorides and CO2.

Graphical abstract: Well-defined chiral dinuclear copper-catalyzed tandem asymmetric propargylic amination–carboxylative cyclization sequence toward chiral 2-oxazolidinone derivatives
Research Article

Entropy effects in temperature-regulated nickel-catalyzed regiodivergent alkene hydroalkylation

Density functional theory calculation studies reveal entropy effects in temperature-regulated nickel-catalyzed regiodivergent alkene hydroalkylation.

Graphical abstract: Entropy effects in temperature-regulated nickel-catalyzed regiodivergent alkene hydroalkylation
Open Access Research Article

A convergent paired electrochemical strategy for decarboxylative C(sp2)–C(sp3) bond formation

In this report, we describe a convergent paired electrochemical decarboxylative C(sp2)–C(sp3) cross-coupling reaction that employs readily available alkyl carboxylic acids and C(sp2)–iodides as direct coupling partners.

Graphical abstract: A convergent paired electrochemical strategy for decarboxylative C(sp2)–C(sp3) bond formation
Research Article

Nickel/photoredox dual-catalyzed reductive cross-coupling of aryl halides and aldehydes

A photoredox-assisted nickel-catalyzed reductive coupling of aryl halides and aldehydes to afford silyl-protected alcohols is reported. Key to success of this strategy is to identify α-silylamines as efficient organic reductants.

Graphical abstract: Nickel/photoredox dual-catalyzed reductive cross-coupling of aryl halides and aldehydes
Research Article

Facile and practical access to chiral benzofused oxa-heterocycles via an asymmetric hydrogenation and intramolecular SNAr cascade

Herein, we report a tandem asymmetric hydrogenation and SNAr reaction, providing valuable six- and five-membered chiral benzofused cyclic ethers with high yields and enantioselectivities (up to 99% yield and up to 99% ee).

Graphical abstract: Facile and practical access to chiral benzofused oxa-heterocycles via an asymmetric hydrogenation and intramolecular SNAr cascade
Open Access Research Article

Pulsed electrolysis: enhancing primary benzylic C(sp3)–H nucleophilic fluorination

Pulsed electrolysis waveforms benefit primary benzylic cation generation and fluorination.

Graphical abstract: Pulsed electrolysis: enhancing primary benzylic C(sp3)–H nucleophilic fluorination
Research Article

Enantio- and diastereoselective conjugate addition of pyridyl alkyl ketones to enones by Cu(II)-Lewis acid/Brønsted base catalysis

Cu(II) Lewis acid/Brønsted base catalysis was employed to achieve enantio- and diastereoselective conjugate additions of pyridyl alkyl ketones to enones, resulting in the formation of various 1,5-diketones with vicinal stereocenters.

Graphical abstract: Enantio- and diastereoselective conjugate addition of pyridyl alkyl ketones to enones by Cu(ii)-Lewis acid/Brønsted base catalysis
Open Access Research Article

Asymmetric copper-catalyzed alkynylallylic dimethylamination

A reliable protocol for asymmetric Cu-catalyzed alkynylallylic dimethylamination is described with the discovery of tetramethyldiaminomethane as a new, stable and convenient surrogate of the dimethylamine nucleophile.

Graphical abstract: Asymmetric copper-catalyzed alkynylallylic dimethylamination
15 items

About this collection

Organic  Chemistry Frontiers is pleased to publish this Emerging Investigator Series to highlight early-career scientists and their excellent research at the forefront of organic chemistry.

Scientists featured in the collection are recognized for the high novelty of their research, their outstanding contributions made during independent career stages, as well as the potential to influence chemistry in future.

More details about the Emerging Investigator Series can be found below, including details on how to apply for considerations. This collection will be updated when new Emerging Investigator Series papers are published – so keep checking this page and watch the collection grow!

Check out the call for papers by Organic Chemistry FrontiersMaterials Chemistry Frontiers and Inorganic Chemistry Frontiers.

Explore the Organic Chemistry Frontiers Emerging Investigator Series 20222023

Spotlight

Advertisements