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Article
| Open AccessNoncovalent interaction with a spirobipyridine ligand enables efficient iridium-catalyzed C–H activation
Exploitation of noncovalent interactions has received much attention for the design of metal catalysts. However, because of the weak nature, CH-π interactions have been less utilized for the control of organic reactions. Here, the authors report that the CH-π interaction can be used to kinetically accelerate catalytic C-H activation of arenes.
- Yushu Jin
- , Boobalan Ramadoss
- & Laurean Ilies
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Article
| Open AccessStress-induced ordering evolution of 1D segmented heteronanostructures and their chemical post-transformations
The formation mechanisms for periodic heterostructures are still poorly understood. Here, the authors propose a versatile approach to synthesize one-dimensional segmented heterostructures and reveal a stress-induced ordering mechanism through phase-field simulations.
- Qing-Xia Chen
- , Yu-Yang Lu
- & Shu-Hong Yu
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Article
| Open AccessCarbon dioxide capture and functionalization by bis(N-heterocyclic carbene)-borylene complexes
Bis(N-heterocyclic carbene)-borylene complexes are capable of capturing and functionalizing CO2, but stable single-site-boron-carbon dioxide adducts are rarely reported. Here, the authors report the synthesis of a stable borylene-CO2 complex as well as the functionalization of the captured CO2.
- Jun Fan
- , An-Ping Koh
- & Cheuk-Wai So
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Article
| Open AccessClosed-loop recycling of sulfur-rich polymers with tunable properties spanning thermoplastics, elastomers, and vitrimers
Sulfur-rich polymers are promising candidates for chemical recycling but lack efficient synthetic strategies for achieving diverse structures. Here, the authors report a synthesis strategy for polytrithiocarbonates which is compatible with a wide range of monomers enabling diverse structures via polycondensation of dithiols and dimethyl trithiocarbonate.
- Jin-Zhuo Zhao
- , Tian-Jun Yue
- & Wei-Min Ren
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Article
| Open AccessLaMg6Ga6S16: a chemical stable divalent lanthanide chalcogenide
Synthesising chemically stable divalent lanthanide compounds is still faced by great challenges. Here, by using octahedra coupling tetrahedra single/double chains to construct an octahedral crystal field, authors synthesised a stable crystalline La(II)-chalcogenide, LaMg6Ga6S16.
- Yujie Zhang
- , Jiale Chen
- & Hongwei Yu
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Article
| Open AccessExtending carbon chemistry at high-pressure by synthesis of CaC2 and Ca3C7 with deprotonated polyacene- and para-poly(indenoindene)-like nanoribbons
The authors demonstrate that carbides with infinite chains of fused [C6] and [C5] rings are synthesized at deep planetary pressures and temperatures. Hydrolysis of these carbides may lead to polycyclic aromatic hydrocarbons in the Universe.
- Saiana Khandarkhaeva
- , Timofey Fedotenko
- & Leonid Dubrovinsky
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Article
| Open AccessStereoselective assembly of C-oligosaccharides via modular difunctionalization of glycals
C-oligosaccharides are found in natural products and drug molecules, but their synthesis is challenging. Here, the authors report a strategy for the stereoselective and efficient synthesis of Coligosaccharides via palladium-catalyzed nondirected C1–H glycosylation/C2-alkenylation, cyanation, and alkynylation of 2-iodoglycals with glycosyl chloride donors.
- Ya-Nan Ding
- , Mei-Ze Xu
- & Yong-Min Liang
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Article
| Open AccessNi-catalyzed enantioconvergent deoxygenative reductive cross-coupling of unactivated alkyl alcohols and aryl bromides
The direct reductive coupling of alkyl alcohol and aryl halide enables efficient access to valuable compounds, but the asymmetric pattern remains unknown. Here the authors describe the enantioconvergent deoxygenative reductive cross-coupling of unactivated alkyl alcohol and aryl bromide in the presence of an NHC activating agent.
- Li-Li Zhang
- , Yu-Zhong Gao
- & Ze-Peng Yang
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Article
| Open AccessEnantioselective total synthesis of (‒)-lucidumone enabled by tandem prins cyclization/cycloetherification sequence
The Ganoderma meroterpenoids are a growing class of natural products with a wide range of biological activities. Here, the authors report the enantioselective total synthesis of the Ganoderma meroterpenoid (‒)-lucidumone, featuring a copper-catalyzed enantioselective silicon-tethered intramolecular Diels-Alder cycloaddition to assemble the bicyclo[2.2.2]octane framework and a domino deprotection/Prins reaction/cycloetherification/oxidation sequence to generate concurrenly the tetrahydrofuran and the fused indanone skeleton.
- Xian-Zhang Liao
- , Ran Wang
- & Guang Li
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Article
| Open AccessMetal free cross-dehydrogenative N-N coupling of primary amides with Lewis basic amines
While the homo N-N coupling of two NH moieties to form the hydrazide N-N bond is well developed, the crossdehydrogenative hetero N-N coupling remains unevolved. Here the authors present an efficient, PhI(OAc)2-mediated intermolecular N-N cross-coupling of primary benzamides with primary and secondary amines.
- Subban Kathiravan
- , Prakriti Dhillon
- & Ian A. Nicholls
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Article
| Open AccessReduction of Li+ within a borate anion
Chemical reduction of alkali cations to their metals is extremely challenging. Here, the authors synthesized a series of redox-active borate anions stabilized by bipyridine ligands which can reduce lithium ions generating elemental lithium metal and borate radicals.
- Haokun Li
- , Jiachen Yao
- & Zhenpin Lu
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Article
| Open AccessEfficient palladium-catalyzed electrocarboxylation enables late-stage carbon isotope labelling
Carbon isotope labelling of bioactive molecules is essential for accessing the pharmacokinetic and pharmacodynamic properties of new drug entities. Here, the authors propose an electrochemical isotope-labelling protocol which enables the use of near-stoichiometric 14CO2, facilitating late-stage and single-step carbon-14 labelling of pharmaceuticals and representative precursors.
- Gabriel M. F. Batista
- , Ruth Ebenbauer
- & Troels Skrydstrup
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Article
| Open AccessA concise and scalable chemoenzymatic synthesis of prostaglandins
Prostaglandins are of interest to synthetic chemists due to their biological activities. Here, the authors present a concise chemoenzymatic synthesis method for several representative prostaglandins, achieved in 5 to 7 steps, via the common intermediate bromohydrin, a radical equivalent of Corey lactone.
- Yunpeng Yin
- , Jinxin Wang
- & Jian Li
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Article
| Open AccessAsymmetric synthesis of P-stereogenic phosphindane oxides via kinetic resolution and their biological activity
P-stereogenic heterocycles are privileged chiral ligands and bioactive compounds, but the catalytic asymmetric synthesis of P-stereogenic phosphindane derivatives is challenging. Here, the authors report a catalytic kinetic resolution of phosphindole oxides via rhodium-catalyzed diastereo- and enantioselective conjugate addition to access enantiopure Pstereogenic phosphindane and phosphindole derivatives.
- Long Yin
- , Jiajia Li
- & Dong Guo
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Article
| Open AccessTargeted sampling of natural product space to identify bioactive natural product-like polyketide macrolides
Polyketide macrolides are of interest for drug discovery but their inherent structural and stereochemical complexity hinders the exploration of related regions of chemical space more broadly. Here, the authors designed in silico and synthesized a library of tetrahydrofuran-containing polyketide macrolides, and screened them against a panel of biological assays, identifying biologically active library members.
- Darryl M. Wilson
- , Daniel J. Driedger
- & Robert A. Britton
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Article
| Open AccessSynthesis of meta-carbonyl phenols and anilines
Phenols and anilines are of extreme importance for medicinal chemistry and material science but the selective preparation of meta-substituted phenols and anilines remains challenging. Here the authors report an efficient copper-catalyzed dehydrogenation strategy to exclusively synthesize meta-carbonyl phenols and anilines from carbonyl substituted cyclohexanes.
- Bao-Yin Zhao
- , Qiong Jia
- & Yong-Qiang Wang
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Article
| Open AccessPhenol as proton shuttle and buffer for lithium-mediated ammonia electrosynthesis
The proton shuttle plays a critical role in the proton transfer process during lithium-mediated ammonia synthesis. Here, the authors establish the structure-activity relationship and design principles for effective proton shuttles.
- Xianbiao Fu
- , Aoni Xu
- & Ib Chorkendorff
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Article
| Open AccessValence-isomer selective cycloaddition reaction of cycloheptatrienes-norcaradienes
Combining data science and organic synthesis to achieve the rapid and precise creation of complex molecules while controlling multiple selectivities is an emerging trend, but few successful examples are reported. Here, the authors develop an artificial neural network regression model using bond orbital data to predict chemical reactivities.
- Shingo Harada
- , Hiroki Takenaka
- & Tetsuhiro Nemoto
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Article
| Open AccessCharacterization of elusive rhamnosyl dioxanium ions and their application in complex oligosaccharide synthesis
Characterizing highly-reactive glycosyl cation intermediates and understanding their glycosylation mechanisms are essential to the stereoselective synthesis of complex carbohydrates. Here the authors report a workflow that is utilized to characterize rhamnosyl 1,3-bridged dioxanium ions derived from C-3 p-anisoyl esterified donors.
- Peter H. Moons
- , Floor ter Braak
- & Thomas J. Boltje
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Article
| Open AccessStabilization of N6 and N8 anionic units and 2D polynitrogen layers in high-pressure scandium polynitrides
The authors discover high-pressure Sc2N6, Sc2N8, and ScN5 polynitrides, synthesized at high pressure and temperature conditions, featuring a unique nitrogen catenation and previously unknown N66− anions, N86− anions and anionic corrugated 2D-polynitrogen layers.
- Andrey Aslandukov
- , Alena Aslandukova
- & Leonid Dubrovinsky
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Article
| Open AccessDioxygen compatible electron donor-acceptor catalytic system and its enabled aerobic oxygenation
The photochemical properties of Electron Donor-Acceptor (EDA) complexes present exciting opportunities, but often require an inert atmosphere to maintain high efficiency. Here, the authors develop a photocatalytic system through rational design, which overcomes the oxygen-sensitive limitation of traditional EDA photocatalytic systems.
- Jialiang Wei
- , Junhong Meng
- & Ning Jiao
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Article
| Open AccessDimethyl sulfate and diisopropyl sulfate as practical and versatile O-sulfation reagents
O-Sulfation is a vital post-translational modification in bioactive molecules, yet there are significant challenges for the synthesis. Here, the authors report a general and robust approach to O-sulfation by harnessing the tunable reactivity of dimethyl sulfate or diisopropyl sulfate under tetrabutylammonium bisulfate activation.
- Shuaishuai Yue
- , Guoping Ding
- & Jiakun Li
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Article
| Open AccessGeneral alkyl fluoride functionalization via short-lived carbocation-organozincate ion pairs
Many alkyl fluorides are readily available, but the synthetic applications trail behind the widely accepted utility of other halides. Here, the authors report a practical Csp3-F bond functionalization method that expands the currently restricted synthetic space of unactivated C(sp3)-F bonds, but also uses benzylic, propargylic and acyl fluorides.
- D. Lucas Kane
- , Bryan C. Figula
- & Christian Wolf
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Article
| Open AccessZirconium and hafnium catalyzed C–C single bond hydroboration
Selective cleavage and subsequent functionalization of C−C single bonds present a fundamental challenge, and the use of inexpensive and Earth-abundant group IV metals for catalytic C−C single-bond cleavage is largely underdeveloped. Here, the authors report zirconium-catalyzed C−C single-bond cleavage and subsequent hydroboration reactions.
- Sida Li
- , Haijun Jiao
- & Lipeng Wu
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Article
| Open AccessTuning light-driven oxidation of styrene inside water-soluble nanocages
Selective functionalization of C(sp2)–H bonds under ambient conditions is a persistent synthetic challenge in organic chemistry. Here the authors combine host-guest charge-transfer-based photoredox chemistry with supramolecular nano-confinement to achieve selective carbonylation of styrene by tuning the dioxygen concentration.
- Souvik Ghosal
- , Ankita Das
- & Jyotishman Dasgupta
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Article
| Open AccessMirror-image ligand discovery enabled by single-shot fast-flow synthesis of D-proteins
Mirror-image phage display has the potential for high-throughput generation of biologically stable macrocyclic D-peptide binders but is hindered by the optimization required for D-protein chemical synthesis. Here, the authors report a general mirror-image phage display pipeline based on automated flow peptide synthesis and use it to prepare and characterize 12 L/D-protein pairs.
- Alex J. Callahan
- , Satish Gandhesiri
- & Bradley L. Pentelute
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Article
| Open AccessNickel-catalyzed electrophiles-controlled enantioselective reductive arylative cyclization and enantiospecific reductive alkylative cyclization of 1,6-enynes
Transition metal-catalyzed asymmetric cyclization of 1,6-enynes is a powerful tool for the construction of chiral nitrogen-containing heterocycles, but limiting to the use of aryl or alkenyl metal reagents. Here, the authors report Ni-catalyzed enantioselective anti-arylative cyclization and enantiospecific cis-alkylative cyclization of 1,6-enynes.
- Wenfeng Liu
- , Yunxin Xing
- & Kun Shen
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Article
| Open AccessRemote-carbonyl-directed sequential Heck/isomerization/C(sp2)–H arylation of alkenes for modular synthesis of stereodefined tetrasubstituted olefins
The synthesis of highly substituted olefins has been pursued for decades. Here, the authors show a carbonyl-directed sequential Heck/isomerization/C–H arylation of alkenes for modular synthesis of stereodefined all-carbon tetrasubstituted olefins.
- Runze Luan
- , Ping Lin
- & Weiping Su
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Article
| Open AccessSpontaneous crystallization of strongly confined CsSnxPb1-xI3 perovskite colloidal quantum dots at room temperature
Photoactive pure-iodine all-inorganic colloidal perovskite quantum dots (QDs) are attractive for optoelectronic applications, however their synthesis at room temperature is challenging. Here the authors report a room temperature strongly confined strategy to synthesize CsSnxPb1-xI3 QDs.
- Louwen Zhang
- , Hai Zhou
- & Guojia Fang
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Article
| Open AccessCooperative Cu/azodiformate system-catalyzed allylic C–H amination of unactivated internal alkenes directed by aminoquinoline
The oxidative intermolecular amination of C-H bonds represents a straightforward method to construct aliphatic allylic amines. However, the utilization of widely available internal alkenes remains a synthetic challenge. Here, the authors present a regioselective Cu-catalyzed oxidative allylic C-H amination of internal olefins with azodiformates.
- Le Wang
- , Cheng-Long Wang
- & Shu-Yu Zhang
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Article
| Open AccessIron-catalyzed fluoroalkylative alkylsulfonylation of alkenes via radical-anion relay
Stoichiometric amounts of metal reductant and the requirement of a directing group limit the application of transition metal-catalyzed reductive difunctionalization of alkenes with alkyl halides. Here, the authors report a reductive difunctionalization of alkenes via a radical-anion relay with Na2S2O4 as both reductant and sulfone-source.
- Xiaoya Hou
- , Hongchi Liu
- & Hanmin Huang
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Article
| Open AccessCircular olefin copolymers made de novo from ethylene and α-olefins
Although several advances have been made in chemical Polyethylene (PE) re- and upcycling, energy-efficient and selective catalytic processes are still lacking. Here, the authors show coupling of an industrially relevant coordination copolymerization olefins with a functionalized chain-transfer agent, followed by modular assembly of the resulting telechelic polyolefin building blocks by polycondensation to afford ester-linked PE-based random and block copolymers which exhibit full chemical circularity.
- Xing-Wang Han
- , Xun Zhang
- & Yong Tang
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Article
| Open AccessOxygen-tolerant CO2 electroreduction over covalent organic frameworks via photoswitching control oxygen passivation strategy
Direct use of flue gas for the electrocatalytic CO2 reduction reaction is desirable but severely limited by the thermodynamically favorable oxygen reduction reaction. Here the authors report an oxygen passivation strategy to improve electrocatalytic CO2 reduction reaction under aerobic conditions using a covalent organic frameworks with a photoswitching unit.
- Hong-Jing Zhu
- , Duan-Hui Si
- & Yuan-Biao Huang
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Article
| Open AccessAccessing ladder-shape azetidine-fused indoline pentacycles through intermolecular regiodivergent aza-Paternò–Büchi reactions
Conformationally rigid 3D molecules are of high interest. Here the authors develop intermolecular aza-Paternò-Büchi reactions to access ladder-shape azetidine-fused indoline pentacycles with excellent regiodivergency and stereoselectivity.
- Jianjian Huang
- , Tai-Ping Zhou
- & Fangrui Zhong
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Perspective
| Open AccessPerformance metrics to unleash the power of self-driving labs in chemistry and materials science
Assessing the performance of self-driving labs (SDLs) is challenging due to the specificities of each experiment. In this Perspective, the authors review recent literature of SDLs for materials science and chemistry and suggest how to report SDL performance more effectively.
- Amanda A. Volk
- & Milad Abolhasani
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Article
| Open AccessAn integrated self-optimizing programmable chemical synthesis and reaction engine
A limitation of robotic platforms in chemistry is the lack of feedback loops to adjust the conditions in-operando. Here the authors present a dynamically programmable robotic system that uses sensors for real-time adaptation, achieving yield improvements in syntheses and discovering new molecules.
- Artem I. Leonov
- , Alexander J. S. Hammer
- & Leroy Cronin
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Article
| Open AccessCarbene organic catalytic planar enantioselective macrolactonization
Macrolactones exhibit distinct conformational and configurational properties and are widely found in natural products but catalysts to govern both macrolactone formation and stereochemical control remain largely unexplored. Here, the authors disclose an N-heterocyclic carbene (NHC)-catalyzed enantioselective synthesis of chiral macrolactones varying in ring size from sixteen to twenty members that feature distinct configurationally stable planar stereogenicity.
- Xiaokang Lv
- , Fen Su
- & Yonggui Robin Chi
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Article
| Open AccessCollective total synthesis of stereoisomeric yohimbine alkaloids
Nature generates the stereoisomeric yohimbine alkaloids using bioavailable monoterpene secolaganin as the building block. Here, the authors reset the stage by the development of a bioinspired coupling, in which the pentacyclic skeleton is constructed through enantioselective kinetic resolution of an achiral, easily accessible synthetic surrogate.
- Meiyi Tang
- , Haigen Lu
- & Liansuo Zu
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Article
| Open AccessMechanochemical synthesis of organoselenium compounds
While the reported methods for the synthesis of organoselenium compounds mainly employ preformed activated selenium reagents, the direct utilization of elemental selenium in the synthesis is a more attractive but challenging strategy. Here, the authors report the rapid synthesis of versatile organoselenium compounds via mechanical stimulation.
- Shanshan Chen
- , Chunying Fan
- & Xiaofeng Wei
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Article
| Open AccessUnified metal-free intermolecular Heck-type sulfonylation, cyanation, amination, amidation of alkenes by thianthrenation
Direct and site-selective C–H functionalization of alkenes under environmentally benign conditions represents a useful and attractive yet challenging transformation to access value-added molecules. Here, the authors report a protocol for a variety of intermolecular Heck-type functionalization of C(sp2)–H bond of alkenes by thianthrenation.
- Ming-Shang Liu
- , Hai-Wu Du
- & Wei Shu
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Article
| Open AccessPredictive Minisci late stage functionalization with transfer learning
Regioselectivity prediction for many reactions remains a challenging target for a priori prediction. Here, the authors develop a machine learning model that predicts the outcomes of Minisci reactions.
- Emma King-Smith
- , Felix A. Faber
- & Alpha A. Lee
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Article
| Open AccessC−F bond activation enables synthesis of aryl difluoromethyl bicyclopentanes as benzophenone-type bioisosteres
Bioisosteric design has become an essential approach during drug molecule discovery process. Here, the authors describe a strategy for defluorinative couplings of propellanes, enabling the synthesis of aryl difluoromethyl bicyclopentanes as benzophenone-type bioisosteres.
- Mingshuo Chen
- , Yuang Cui
- & Xiaheng Zhang
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Article
| Open AccessHelical-caging enables single-emitted large asymmetric full-color circularly polarized luminescence
Circularly polarised luminescence (CPL) is essential for asymmetric synthetic photochemistry. Here, the authors integrate white quantum dots with chiral nematic liquid crystal or liquid crystal polymer to achieve single-emitted tuneable full-colour or white CPL for enantioselective polymerization.
- Yajie Zhou
- , Yaxin Wang
- & Taotao Zhuang
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Article
| Open AccessSelf-assembly of the smallest and tightest molecular trefoil knot
The synthesis of molecular knots remains challenging. Here, the authors report the synthesis of a chiral molecular trefoil metallaknot by self-assembly which contains only 54 atoms in the backbone.
- Zhiwen Li
- , Jingjing Zhang
- & Richard J. Puddephatt
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Article
| Open AccessStructural regulation of halide superionic conductors for all-solid-state lithium batteries
Predicting the structure of lithium halide solid-state electrolytes from their composition alone is a challenge. Here, the authors introduce the “cationic polarization factor” that captures the key interactions of halide-based solid-state electrolytes and predicts the stacking structures.
- Xiaona Li
- , Jung Tae Kim
- & Xueliang Sun
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Article
| Open AccessAtroposelective hydroarylation of biaryl phosphines directed by phosphorus centres
Directing group strategies have been used extensively in C–H activation reactions but current methods rely heavily on coordination with nitrogen or oxygen atoms in molecules and have therefore been found to exhibit limited generality in asymmetric syntheses. Here, the authors report enantioselective C–H activation with unsaturated hydrocarbons directed by phosphorus centres to rapidly construct libraries of axially chiral phosphines through dynamic kinetic resolution.
- Zexian Li
- , Minyan Wang
- & Zhuangzhi Shi
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Article
| Open AccessC5 methylation confers accessibility, stability and selectivity to picrotoxinin
Minor changes to complex structures can exert major influences on synthesis strategy and functional properties but synthetic difficulties can obstruct the exploration of natural product function. Here the authors explore two parallel series of picrotoxinin analogs and identify leads with selectivity between mammalian and insect ion channels.
- Guanghu Tong
- , Samantha Griffin
- & Ryan A. Shenvi
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Article
| Open AccessElectroreductive hydroxy fluorosulfonylation of alkenes
As sulfonyl fluorides have found wide applications, synthetic access to β-hydroxy sulfonyl fluorides is desirable. Here, the authors report an electroreductive strategy for radical hydroxyl fluorosulfonylation of alkenes with sulfuryl chlorofluoride and molecular oxygen from air.
- Qingyuan Feng
- , Tianyu He
- & Shenlin Huang
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Article
| Open AccessTotal wash elimination for solid phase peptide synthesis
Peptide drug manufacturing commonly uses large amounts of hazardous solvents primarily due to multiple washings after each step. Here, the authors introduce the concept of a completely wash-free methodology that enables up to 95% waste reduction.
- Jonathan M. Collins
- , Sandeep K. Singh
- & Christopher L. Houser
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