Themed collection 2026 Organic Chemistry Frontiers Review-type Articles
From acyl boronates to functional boronate-substituted and boron-containing heterocycles: emerging methods and applications
Over the past decade, acyl boronates have emerged as versatile precursors in organic synthesis, facilitating the construction of diverse and important classes of compounds, including boronate-substituted and boron-containing heterocycles.
Org. Chem. Front., 2026,13, 1927-1937
https://doi.org/10.1039/D5QO01583A
Carbon isotope exchange and transfer reactions involving CO2
A review covering early studies to the latest development in carbon isotope exchange and transfer reactions involving CO2.
Org. Chem. Front., 2026, Advance Article
https://doi.org/10.1039/D6QO00133E
Strong Base-Induced Transition-Metal-Free Single Electron Transfer Reactions Mediated by Amine Species
Org. Chem. Front., 2026, Accepted Manuscript
https://doi.org/10.1039/D6QO00136J
Allylic alcohols in borrowing hydrogen catalysis: from simple substrates to complex molecules
Org. Chem. Front., 2026, Accepted Manuscript
https://doi.org/10.1039/D6QO00148C
Photocatalytic Precision Editing of Amino Acid Residues: Advances, Mechanisms, and Future Directions
Org. Chem. Front., 2026, Accepted Manuscript
https://doi.org/10.1039/D6QO00346J
Recent advances in visible-light-induced defluorinative functionalization of α-trifluoromethyl arylalkenes
In this perspective, we summarize recent advances in visible-light-driven defluorinative functionalization of α-trifluoromethyl arylalkenes, highlighting the strategies for gem-difluoroalkene synthesis via photoinduced SET and radical–polar crossover.
Org. Chem. Front., 2026,13, 2178-2200
https://doi.org/10.1039/D5QO01732G
Synthesis of chiral α-trifluoromethyl amines via asymmetric reactions of trifluoromethylated imines
A review of recent research progress in the synthesis of α-trifluoromethyl amines through the asymmetric reduction of trifluoromethylated imines and nucleophilic addition to trifluoromethylated imines.
Org. Chem. Front., 2026,13, 2159-2177
https://doi.org/10.1039/D6QO00001K
Oxidation reactions in the current total synthesis of natural products
The oxidation reactions employed in selected total syntheses from 2020 to 2025 are surveyed to reflect their current status, guide planning in total syntheses, and prompt organic chemists to develop more efficient oxidation reactions and reagents.
Org. Chem. Front., 2026, Advance Article
https://doi.org/10.1039/D6QO00050A
Fluoroalkylation of steroid derivatives: synthetic strategies, mechanistic trends, and pharmacological perspectives
Fluorinated steroid chemistry evolved from a niche field into a central discipline linking organic synthesis, medicinal chemistry, and chemical biology. Advances in mechanisms, reagents, and selectivity will expand tools for drug discovery.
Org. Chem. Front., 2026,13, 1938-1963
https://doi.org/10.1039/D5QO01669J
Recent advances in earth-abundant transition-metal-catalysed asymmetric oxidative sp3–sp3 cross-couplings
This review summarizes advances in earth-abundant transition-metal-catalyzed asymmetric oxidative sp3–sp3 cross-couplings, focusing on reaction development, mechanistic insights, synthetic applications, key challenges, and future perspectives.
Org. Chem. Front., 2026,13, 1703-1723
https://doi.org/10.1039/D5QO01749A
Transition metal-catalyzed selective hydroalkynylation of internal alkynes with terminal alkynes
This review highlights recent advances in transition-metal-catalyzed hydroalkynylation of internal alkynes, outlining emerging strategies and future prospects.
Org. Chem. Front., 2026,13, 1688-1702
https://doi.org/10.1039/D5QO01640A
Enantioselective synthesis of atropisomeric biaryls and heterobiaryls via transition metal-catalyzed cyclization
Atropisomeric architectures with a chiral axis are prevalent in biologically active molecules and natural products, and they are widely put to use in privileged catalysts and chiral ligands.
Org. Chem. Front., 2026, Advance Article
https://doi.org/10.1039/D5QO01492A
Polysubstituted bicyclo-[2.1.1]-hexanes as benzene isosteres for medicinal chemistry
This comprehensive review describes the methodologies reported between 2020 and early 2025 for the synthesis of (hetero)bicyclo[2.1.1]hexane derivatives, organised by mechanisms and the exit vectors achieved.
Org. Chem. Front., 2026, Advance Article
https://doi.org/10.1039/D5QO01662B
Advances in the construction of boryl cyclobutanes
Recent advances in the synthesis of boryl-substituted cyclobutanes are summarized, highlighting strain-release, boronate complex reactivity, 1,2-migration, and catalytic strategies for stereocontrolled access to sp3-rich building blocks.
Org. Chem. Front., 2026, Advance Article
https://doi.org/10.1039/D6QO00008H
Radical reactivity of aryl thianthrenium salts
Aryl thianthrenium salts, accessed through highly selective arene thianthrenation, offer a versatile platform for generating aryl radicals under mild conditions, enabling streamlined C–D, C–C, and C–heteroatom bond formation among diverse substrates.
Org. Chem. Front., 2026,13, 1424-1457
https://doi.org/10.1039/D5QO01417D
Recent advances in asymmetric dearomatization of nitro(hetero)arenes
We summarize recent advances in nitro(hetero)arenes-enabled CADA, with a detailed discussion of diverse types of reactions, involving asymmetric cycloaddition, asymmetric Michael addition, and asymmetric interrupted Barton-Zard reaction.
Org. Chem. Front., 2026,13, 1458-1480
https://doi.org/10.1039/D5QO01566A
About this collection
<span lang="zh-CN" style="font-family:Arial">Critical reviews and chemistry frontiers articles published in </span><span lang="en-US" style="font-family:Arial">O</span><span lang="en-US" style="font-family:"Microsoft YaHei"">rganic </span><span lang="zh-CN" style="font-family:Arial">Chemistry Frontiers during 202</span><span lang="en-US" style="font-family:Arial">6</span><span lang="zh-CN" style="font-family:Arial"> are collated as below for the benefit of readers.</span>