Featured
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Regioselective hydroformylation of propene catalysed by rhodium-zeolite
Rhodium catalysts confined in zeolite pores exhibit high regioselectivity in the hydroformylation process of propene to high-value n-butanal, surpassing the performance of all heterogeneous and most homogeneous catalysts developed so far.
- Xiangjie Zhang
- , Tao Yan
- & Zhi Cao
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News & Views |
Trio of radicals choreographed for versatile chemical reaction
The idea that three different free radicals could be used together to carry out specific steps in a chemical reaction has long been implausible. A ‘radical sorting’ strategy now achieves this feat to make organic molecules.
- Kenneth F. Clark
- & John A. Murphy
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Research Briefing |
‘Bandit’ algorithms help chemists to discover generally applicable conditions for reactions
In organic chemistry, finding conditions that enable a broad range of compounds to undergo a particular type of reaction is highly desirable. However, conventional methods for doing so consume a lot of time and reagents. A machine-learning method has been developed that overcomes these problems.
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Identifying general reaction conditions by bandit optimization
Bandit optimization models are used to identify generally applicable conditions by efficient condition sampling and evaluation of experimental feedback.
- Jason Y. Wang
- , Jason M. Stevens
- & Abigail G. Doyle
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Article
| Open AccessStereodivergent 1,3-difunctionalization of alkenes by charge relocation
We introduce a method for the direct 1,3-difunctionalization of alkenes, based on a concept termed ‘charge relocation’, which enables stereodivergent access to 1,3-difunctionalized products of either syn- or anti-configuration from unactivated alkenes.
- Bogdan R. Brutiu
- , Giulia Iannelli
- & Nuno Maulide
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| Open AccessCatalytic asymmetric cationic shifts of aliphatic hydrocarbons
We describe an imidodiphosphorimidate-catalysed asymmetric Wagner–Meerwein shift of aliphatic alkenyl cycloalkanes to cycloalkenes with excellent regio- and enantioselectivity.
- Vijay N. Wakchaure
- , William DeSnoo
- & Benjamin List
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News |
This GPT-powered robot chemist designs reactions and makes drugs — on its own
A system called Coscientist scours the Internet for instructions, then designs and executes experiments to synthesize molecules.
- Katharine Sanderson
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Article |
A light-driven enzymatic enantioselective radical acylation
Enzyme-bound ketyl radicals derived from thiamine diphosphate are selectively generated through single-electron oxidation by a photoexcited organic dye and shown to lead to enantioselective radical acylation reactions.
- Yuanyuan Xu
- , Hongwei Chen
- & Xiaoqiang Huang
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News & Views |
Carbon rings push limits of chemical theories
Scientists are tantalized by the many forms that carbon could adopt — some of which are predicted to have extraordinary properties. The synthesis of three new all-carbon molecules is therefore a source of excitement.
- Przemysław Gaweł
- & Cina Foroutan-Nejad
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Computational prediction of complex cationic rearrangement outcomes
Computers equipped with a comprehensive knowledge-base of mechanistic steps augmented by physical-organic chemistry rules, as well as quantum mechanical and kinetic calculations, can use a reaction-network approach to analyse the mechanisms of cationic rearrangements.
- Tomasz Klucznik
- , Leonidas-Dimitrios Syntrivanis
- & Bartosz A. Grzybowski
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News & Views |
Atom-swap chemistry could aid drug discovery
An unconventional route for modifying pharmaceutically relevant molecules swaps an atom of carbon for one of nitrogen. The resulting derivatives might open up avenues of research in medicinal-chemistry campaigns.
- Filippo Ficarra
- & Mattia Silvi
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Complex molecule synthesis by electrocatalytic decarboxylative cross-coupling
We report a radical-based Ni/Ag-electrocatalytic cross-coupling of substituted carboxylic acids, enabling an approach to accessing complex molecular architectures, which relies on a silver additive that forms an active Ag nanoparticle-coated electrode surface along with carefully chosen ligands.
- Benxiang Zhang
- , Jiayan He
- & Phil S. Baran
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Research Briefing |
The chemical synthesis and anti-cancer properties of portimines
The natural toxins portimine A and B have attracted interest for their unusual chemical architecture and potent anti-cancer activity. The first total synthesis of portimines enables the identification of portimine A’s molecular target and reveals that the toxin induces programmed cell death in human cancer cells.
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High-entropy halide perovskite single crystals stabilized by mild chemistry
Room-temperature-solution (20 °C) and low-temperature-solution (80 °C) synthesis procedures are developed for a new class of metal halide perovskite high-entropy semiconductor single crystals.
- Maria C. Folgueras
- , Yuxin Jiang
- & Peidong Yang
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Research Briefing |
Multidecker sandwich compounds assembled into nano-rings
Sandwich compounds are molecules in which two planar molecular rings sandwich a metal ion ‘filling’ between them. The chemistry of these compounds has been extended by the assembly of nano-rings from 18 identical sandwich-type building blocks.
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Regioselective aliphatic C–H functionalization using frustrated radical pairs
Regioselective functionalization of aliphatic carbon–hydrogen bonds is achieved using frustrated radical pairs generated from disilazide donors and an N-oxoammonium acceptor.
- Zhipeng Lu
- , Minsoo Ju
- & Song Lin
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Article
| Open AccessPhotocatalytic phosphine-mediated water activation for radical hydrogenation
Using a photocatalytic phosphine-mediated radical process under mild conditions enables direct hydrogen atom transfer to closed-shell π systems for activation of water.
- Jingjing Zhang
- , Christian Mück-Lichtenfeld
- & Armido Studer
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News & Views |
Rarely used strained molecules step up for organic synthesis
Energy released from molecules under strain can promote difficult chemical reactions. A practical method has been developed that uses an overlooked, highly strained compound to rapidly construct complex organic products.
- Fahima I. M. Idiris
- & Christopher R. Jones
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Research Briefing |
Nanoparticles containing diverse elements made using liquid metal
The synthesis of high-entropy alloy nanoparticles (HEA-NPs) — small particles each containing multiple principal metal elements — typically requires extreme conditions to ensure adequate mixing of constituents. Innovative experiments show that the liquid metal can act as a mixing reservoir to facilitate the synthesis of a diverse range of such nanoparticles in mild conditions.
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Research Briefing |
Nickel catalyses a host of chemical reactions in a general method
A minimal but general method has been developed for catalysing many different cross-coupling reactions — those in which two chemical fragments are joined. It requires only the two substrate substances, a nickel salt as a catalyst precursor, a catalyst for light-driven redox reactions and, in some cases, a nitrogen-containing base.
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General cross-coupling reactions with adaptive dynamic homogeneous catalysis
A self-adjustive catalytic system with nickel under visible-light-driven redox reaction conditions provides a general method for carbon–(hetero)atom cross-coupling reactions and is demonstrated for nine different bond-forming reactions.
- Indrajit Ghosh
- , Nikita Shlapakov
- & Burkhard König
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Organic–inorganic covalent–ionic molecules for elastic ceramic plastic
Covalent organic molecules can be combined with ionic inorganic molecules to create a hybrid material demonstrating paradoxical mechanical properties in a bottom-up manner, enabling the manufacture of an ‘elastic ceramic plastic’.
- Weifeng Fang
- , Zhao Mu
- & Zhaoming Liu
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Transannular C–H functionalization of cycloalkane carboxylic acids
Quinuclidine-pyridone and sulfonamide-pyridone ligands enable transannular γ-methylene C–H arylation of cycloalkane carboxylic acids with a range of ring sizes, bringing us closer to molecular editing of saturated carbocycles.
- Guowei Kang
- , Daniel A. Strassfeld
- & Jin-Quan Yu
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Strain-promoted reactions of 1,2,3-cyclohexatriene and its derivatives
The strained C6H6 isomer 1,2,3-cyclohexatriene and its derivatives participate in a host of reaction modes which demonstrate their potential for selective chemical transformations and provide an unconventional entryway to complex scaffolds.
- Andrew V. Kelleghan
- , Ana S. Bulger
- & Neil K. Garg
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Copper-catalysed enantioconvergent alkylation of oxygen nucleophiles
The enantioconvergent alkylation of oxygen nucleophiles is achieved using α-haloamides and a readily available copper catalyst, and the reaction proceeds under mild conditions in the presence of a wide variety of functional groups.
- Caiyou Chen
- & Gregory C. Fu
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Research Briefing |
A method to make inorganic membranes on the surface of aqueous solutions
A generalizable technique has been developed to create diverse functional inorganic membranes on the surface of various aqueous solutions. The technique ensures that the air–liquid interface receives a continuous supply of floating particles, which then assemble dynamically to form continuous membranes.
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Mechanistic formulation of inorganic membranes at the air–liquid interface
By switching the nucleation preferences in aqueous systems of inorganic precursors to bias formation and growth at the air–liquid interface, the mechanistic formation of inorganic membranes from the floating-particle system is demonstrated.
- Chen Zhang
- , Wanheng Lu
- & Ghim Wei Ho
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Enantioconvergent Cu-catalysed N-alkylation of aliphatic amines
The chemoselective and enantioconvergent N-alkylation of aliphatic amines, including ammonia, is achieved using chiral tridentate anionic ligands and a copper catalyst; the method shows excellent enantioselectivity and functional-group tolerance.
- Ji-Jun Chen
- , Jia-Heng Fang
- & Xin-Yuan Liu
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| Open AccessControl of stereogenic oxygen in a helically chiral oxonium ion
The design, synthesis and characterization of a helically chiral triaryloxonium ion is reported, which is an example of a chiral non-racemic and configurationally stable molecule in which the oxygen atom is the sole stereogenic centre.
- Owen Smith
- , Mihai V. Popescu
- & Martin D. Smith
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Electrochemical reactor dictates site selectivity in N-heteroarene carboxylations
An electrochemical strategy is described in which the direct carboxylation of pyridines and related N-heteroarenes with CO2 shows divergent site selectivity depending on the type of reactor used.
- Guo-Quan Sun
- , Peng Yu
- & Song Lin
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A few-layer covalent network of fullerenes
A two-dimensional crystalline polymer of C60, termed graphullerene, is synthesized by chemical vapour transport, and mechanically exfoliated to produce molecularly thin flakes with clean interfaces for potential optoelectronic applications.
- Elena Meirzadeh
- , Austin M. Evans
- & Xavier Roy
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Research Briefing |
Rational discovery of solid materials by tuning a hot two-part solution
High-temperature solutions called fluxes are widely used to synthesize solid compounds. The composition and structural properties of reaction products in a two-component flux system can now be tuned by varying the temperature and the ratio between a component of the reaction medium and a second component that serves as a ‘tuning knob’.
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Discovery of chalcogenides structures and compositions using mixed fluxes
A new methodology for the discovery of chalcogenides by tuning the temperature and flux ratios of systems using mixed fluxes is demonstrated, leading to the synthesis of 30 new and unreported compounds or compositions.
- Xiuquan Zhou
- , Venkata Surya Chaitanya Kolluru
- & Mercouri G. Kanatzidis
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News & Views |
A leap forward in the quest for general catalysts
Truly general chemical reactions work well regardless of the structural features and functional groups in the starting molecule. A new screening protocol speeds up the identification of such reactions in the field of asymmetric catalysis.
- Manuel J. Scharf
- & Benjamin List
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News & Views |
Machine assembly of carbohydrates with more than 1,000 sugar units
Efforts to probe the biological functions of carbohydrates have long been limited by the lack of such molecules with well-defined structures. An automated carbohydrate synthesizer has been developed that could remedy this.
- Hanchao Cheng
- & Peng George Wang
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News & Views |
A stable alternative to an explosive synthetic reaction
The ozonolysis reaction is a classic of organic synthesis, but involves the formation of potentially explosive reaction intermediates. A modern, safer spin on this process makes use of previously overlooked chemistry.
- Vignesh Palani
- & Alison Wendlandt
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Photoexcited nitroarenes for the oxidative cleavage of alkenes
Oxidative cleavage of alkenes is achieved using nitroarenes and light irradiation as an alternative to using ozone to break the carbon–carbon bonds, avoiding the explosive intermediates formed with ozone.
- Alessandro Ruffoni
- , Charlotte Hampton
- & Daniele Leonori
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News & Views |
Synthesis reveals unexpected biological targets of a traditional medicine
A compound made by plants used in traditional medicine has been prepared by chemical synthesis, providing enough for biological testing. The unexpected finding that it acts at opioid receptors raises prospects for drug discovery.
- Nicholas P. R. Onuska
- & Joshua G. Pierce
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Obituary |
David A. Evans (1941–2022)
Chemist who developed ways to synthesize and depict bioactive products.
- Mark Lautens
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News Feature |
Why chemists can’t quit palladium
A retracted paper highlights chemistry’s history of trying to avoid the expensive, toxic — but necessary — catalyst.
- Ariana Remmel
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News & Views |
Multilayer 2D insulator shows promise for post-silicon electronics
A method has been developed for fabricating thin films of the 2D insulator hexagonal boron nitride with a uniform crystal orientation. The advance makes this material a key contender for replacing silica substrates in future electronics.
- Soo Ho Choi
- & Soo Min Kim
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Research Briefing |
A radical way to forge carbon–carbon bonds
Carbon–carbon single bonds are found in most organic molecules. A new electrocatalytic method can create such bonds by uniting different alkyl carboxylic acids, substantially shortening synthetic routes to useful molecules. The reaction uses inexpensive reagents in a simple and scalable set-up, and allows the inclusion of many other functional groups.
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Programmable heating and quenching for efficient thermochemical synthesis
By using a programmable electric current to allow rapid pulsed heating and quenching, a non-equilibrium, continuous synthesis technique shows improved performance in thermochemical reactions, as well as lower energy costs.
- Qi Dong
- , Yonggang Yao
- & Liangbing Hu
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Computer-designed repurposing of chemical wastes into drugs
A forward-synthesis platform, Allchemy, computationally determines how to ‘close the circle’, or use waste chemicals to make valuable pharmaceutical or agrochemical products, ranking possible routes by environmental, geospatial, and other factors.
- Agnieszka Wołos
- , Dominik Koszelewski
- & Bartosz A. Grzybowski
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News & Views |
Electrification promotes tricky synthetic chemical reactions
Chemical synthesis often relies on reactions catalysed by transition metals. Electrochemical methods have now been developed that negate this need, opening up pathways to previously challenging reactions.
- Charlotte Willans
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Metastable hexagonal close-packed palladium hydride in liquid cell TEM
A metastable palladium hydride is synthesized where the unique environment in the liquid cell, namely the limited quantity of Pd precursors and the continuous supply of H, resulted in the formation of the hcp phase.
- Jaeyoung Hong
- , Jee-Hwan Bae
- & Dong Won Chun
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Synthesis of chiral sulfinate esters by asymmetric condensation
A synthetic strategy for the stereoselective preparation of sulfinate esters and related sulfur stereogenic centres via asymmetric condensation expands the drug discovery toolbox for these compounds.
- Xin Zhang
- , Esther Cai Xia Ang
- & Choon-Hong Tan
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Article
| Open AccessTritiation of aryl thianthrenium salts with a molecular palladium catalyst
The isotopic label tritium can be selectively added into aromatic organic compounds by a homogenous hydrogenolysis reaction using aryl thianthrenium salts, tritium gas and a molecular palladium catalyst.
- Da Zhao
- , Roland Petzold
- & Tobias Ritter
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Synthon-based ligand discovery in virtual libraries of over 11 billion compounds
V-SYNTHES, a scalable and computationally cost-effective synthon-based approach to compound screening, identified compounds with a high affinity for CB2 and CB1 in a hierarchical structure-based screen of more than 11 billion compounds.
- Arman A. Sadybekov
- , Anastasiia V. Sadybekov
- & Vsevolod Katritch
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