👉Check out recent #research: Synergistic catalytic allenylic alkylation for #stereodivergent construction of allenes bearing 1,3-axial and central chirality by Xiaohua Liu's team.

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🔓#OpenAccess #metalcatalyst

Read 1,2 Wagner–Meerwein shift in aza-Nazarov cyclization: Bi(iii)-catalyzed substrate-dependent divergent synthesis of highly substituted pyrroles and indenes by Rishikesh Narayan's team.

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👉Check out recent #review: Polyfluorinated reagents for peptide stapling, which focused on three major classes of polyfluorinated reagents: #rylation, #vinylation, and #amidation reagents.

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🔓#OpenAccess #HAT #SET

Check out #research: Beyond HAT: harnessing TBADT for photocatalyzed Giese-type C(sp³)–C(sp³) bond formation through reductive decarboxylation by Maurizio Fagnoni et al. @unipv

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🔥Recent #research by EiC Shengming Ma's team: Copper-catalyzed aerobic oxidation of aldehydes to carboxylic acids, in which an aerobic #oxidation of #aldehydes to #carboxylic acids using O₂ or air as the oxidant has been developed.

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👉Check out recent #research Conformational preference of N-difluoromethylated amides: contributions of hydrogen-bonding, #steric, and #stereoelectronic effects by Ryu Yamasaki et al. @spu_kouhou

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👉Read the #review regarding the #oxetane core #tolerance towards the reaction conditions of the typical toolbox:

Oxetane as a part of modern medicinal chemistry toolbox: the advanced synthesis of 3,3-disubstituted building blocks

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👉Read recent #research meta-Selective thiofluoroalkylation of substituted pyridines via Zincke imines table by @willcdhartley, Omar Boutureira et al. @universitatURV

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Back cover of Issue 11 showcases research from Bappaditya Gole 𝘦𝘵 𝘢𝘭.

"Unveiling stereoselective ladders viaphoto-oligomerization of a diazaanthracene macrocycle"

#Free_to_read
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Inside cover of Issue 11 presents

"Palladium-catalyzed chemoselective decarboxylative coupling of alkynyl carboxylic acids with halogenated aryl triflates" by Chau Ming So 𝘦𝘵 𝘢𝘭.

#Free_to_read
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🔔Issue 11 is available! Please read the cover article:

"Supramolecular catalysis in the dearomative Michael addition involving nitro-group-activated benzofurans" by Anna Skrzyńska, Łukasz Albrecht 𝘦𝘵 𝘢𝘭.

#Free_to_read
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👉Recent #research clarifies the synergistic roles of Ni and Al: Mechanistic insights into Ni–Al co-catalyzed alkyne carbophosphination enabled by C–P bond activation by Congcong Huang, Yishi Lia and Juan Li. @jnu1906

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🔥A #hot #review article by @huangx513's team: Recent advances in repurposing natural enzymes for new-to-nature asymmetric #photobiotransformations, which is also included in the Emerging Investigator Series #EMI of OCF.

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📢Don't miss our CCS-RSC Young Chemist webinar! Meet with Dr. Agnieszka Nowak-Król, Early career advisory board member of Organic Chemistry Frontiers, and other young scientists!
⏰Time: 7:00 am (UK time)
📅Date: May 30, 2025
👉Register here: rsc.zoom.us/webinar/regist…
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Replying to @OrgChemFront
Speakers:
-Liu Liu, Southern University of Science and Technology
-Dawen Niu, Sichuan University
-Yan Qiao, Institute of Chemistry, CAS
-Yuen Wu, University of Science and Technology of China
-Nicola Gasparini, Imperial College London
-Agnieszka Nowak-Król, Universität Würzburg
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OrgChemFront retweeted
Check out our latest review discussing how to make peptide macrocycles using fluorinated reagents. @OrgChemFront

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👉Read #review article Advancements and perspectives toward radical Truce–Smiles-type rearrangement by Yuxi Wang, Chao Shu et al.

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🔥Read #hot #review article regarding: Visible light-mediated #halofunctionalization of alkenes for the synthesis of vicinally functionalized organohalides. By Kanta Pajujantaro, Ying Chena and Gong-Qing Liu. #NTU

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🔥Recent #hot article: Enantioselective catalytic Urech hydantoin synthesis by Yu-Ping He's team, in which an example of asymmetric catalytic UHS is disclosed. Check it out if you are interested!

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OrgChemFront retweeted
Excited to share our latest work published in @OrgChemFront 🥳🥳🥳. We report two new reagents—ATAs and AABs—inspired by the milestone Schmidt and Yu glycosylation strategies, enabling the direct azetidinylation of diverse nucleophiles at any stage.
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