Themed collection Organic Chemistry Frontiers Emerging Investigator Series 2024–2025
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.
Org. Chem. Front., 2025, Advance Article
https://doi.org/10.1039/D4QO02193B
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.
Org. Chem. Front., 2025, Advance Article
https://doi.org/10.1039/D4QO02318H
Access to fluorinated dienes through hydrofluorination of 2-En-4-ynoates
The hydrofluorination of enynoates has been developed for the synthesis of fluorinated dienoates.
Org. Chem. Front., 2025, Advance Article
https://doi.org/10.1039/D4QO02049A
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.
Org. Chem. Front., 2025, Advance Article
https://doi.org/10.1039/D4QO02188F
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.
Org. Chem. Front., 2025, Advance Article
https://doi.org/10.1039/D4QO02097A
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.
Org. Chem. Front., 2024,11, 6617-6626
https://doi.org/10.1039/D4QO01585A
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.
Org. Chem. Front., 2024,11, 6311-6318
https://doi.org/10.1039/D4QO01474J
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.
Org. Chem. Front., 2024,11, 6319-6326
https://doi.org/10.1039/D4QO01368A
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.
Org. Chem. Front., 2024,11, 3648-3654
https://doi.org/10.1039/D4QO00486H
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.
Org. Chem. Front., 2024,11, 1941-1948
https://doi.org/10.1039/D3QO02141F
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.
Org. Chem. Front., 2024,11, 1205-1210
https://doi.org/10.1039/D3QO01927F
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).
Org. Chem. Front., 2024,11, 1118-1123
https://doi.org/10.1039/D3QO01665J
Pulsed electrolysis: enhancing primary benzylic C(sp3)–H nucleophilic fluorination
Pulsed electrolysis waveforms benefit primary benzylic cation generation and fluorination.
Org. Chem. Front., 2024,11, 802-808
https://doi.org/10.1039/D3QO01865B
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.
Org. Chem. Front., 2024,11, 746-754
https://doi.org/10.1039/D3QO01707A
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.
Org. Chem. Front., 2024,11, 690-695
https://doi.org/10.1039/D3QO01749D
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!
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Explore the Organic Chemistry Frontiers Emerging Investigator Series 2022–2023