0 | 1,4‐Aminoarylation of Butadienes via Photoinduced Palladium Catalysis | ACIE |
1 | β‐Phenethylamine Synthesis: N‐Pyridinium Aziridines as Latent Dual Electrophiles | ACIE |
2 | A General Iron‐Catalyzed Decarboxylative Oxygenation of Aliphatic Carboxylic Acids | ACIE |
3 | A Rationally Designed Iron(II) Catalyst for C(sp3)−C(sp2) and C(sp3)−C(sp3) Suzuki–Miyaura Cross‐Coupling | ACIE |
4 | Asymmetric Dearomatization of Indoles through Cobalt‐Catalyzed Enantioselective C−H Functionalization Enabled by Photocatalysis | ACIE |
5 | Cationic Bis(hydrosilane)—Coinage‐Metal Complexes: Synthesis, Characterization, and Use as Catalysts for Outer‐Sphere C=O Hydrosilylation Not Involving Metal Hydrides | ACIE |
6 | Chemoselective and Stereoselective Allylation of Bis(alkenyl)boronates | ACIE |
7 | Conformational Locking Induced Enantioselective Diarylcarbene Insertion into B−H and O−H Bonds Using a Cationic Rh(I)/Diene Catalyst | ACIE |
8 | Construction of Bridged Benzazepines via Photo‐Induced Dearomatization | ACIE |
9 | Copper‐Catalyzed Regiodivergent Asymmetric Difunctionalization of Terminal Alkynes | ACIE |
10 | Copper‐Catalyzed α‐Arylation of Nitroalkanes with (Hetero)aryl Bromides/Iodides | ACIE |
11 | Deconstructive Carboxylation of Activated Alkenes with Carbon Dioxide | ACIE |
12 | Deoxygenative Transformation of Alcohols via Phosphoranyl Radical from Exogenous Radical Addition | ACIE |
13 | Dual‐Catalysed Intermolecular Reductive Coupling of Dienes and Ketones** | ACIE |
14 | Dynamic Asymmetric Diamination of Allylic Alcohols through Borrowing Hydrogen Catalysis: Diastereo‐Divergent Synthesis of Tetrahydrobenzodiazepines | ACIE |
15 | Enantioconvergent Cross‐Nucleophile Coupling: Copper‐Catalyzed Deborylative Cyanation | ACIE |
16 | Enantioconvergent Negishi Cross‐Couplings of Racemic Secondary Organozinc Reagents to Access Privileged Scaffolds: A Combined Experimental and Theoretical Study | ACIE |
17 | Expansion of Structure Property in Cascade Nazarov Cyclization and Cycloexpansion Reaction to Diverse Angular Tricycles and Total Synthesis of Nominal Madreporanone | ACIE |
18 | Exploring Superacid‐Promoted Skeletal Reorganization of Aliphatic Nitrogen‐Containing Compounds | ACIE |
19 | Intramolecular Carboamination of Aminodienes to N‐Heterocycles via C−N Bond Activation | ACIE |
20 | Modular and Diverse Synthesis of Acrylamides by Palladium‐Catalyzed Hydroaminocarbonylation of Acetylene | ACIE |
21 | Molecular Editing of Pyrroles to Benzenes/Naphthalenes by N2O Deletion. | ACIE |
22 | New Frontiers in Organosodium Chemistry as Sustainable Alternatives to Organolithium Reagents | ACIE |
23 | Olefination of Aromatic Carbonyls via Site‐Specific Activation of Cycloalkanone Ketals** | ACIE |
24 | One‐Carbon Ring Expansion of Indoles and Pyrroles: A Straightforward Access to 3‐Fluorinated Quinolines and Pyridines | ACIE |
25 | Palladium(0) and Brønsted Acid Co‐Catalyzed Enantioselective Hydro‐Cyclization of 2,4‐Dienyl Hydrazones and Oximes | ACIE |
26 | Palladium‐Catalyzed Deuteration of Arylketone Oxime Ethers | ACIE |
27 | Photochemical Deoxygenative Hydroalkylation of Unactivated Alkenes Promoted by a Nucleophilic Organocatalyst | ACIE |
28 | Photoexcitation of Distinct Divalent Palladium Complexes in Cross‐Coupling Amination Under Air | ACIE |
29 | Photoinduced Cu(II)‐Mediated Decarboxylative Thianthrenation ofAryl and Heteroaryl Carboxylic Acids | ACIE |
30 | Photoredox‐Catalyzed Generation of Tertiary Anions from Primary Amines via a Radical Polar Crossover | ACIE |
31 | Photoredox‐Catalyzed α−C−H Monoalkylation of Symmetric Polyols in the Presence of CO2 | ACIE |
32 | Regio‐ and Diastereoselective Synthesis of Polysubstituted Piperidines Enabled by Boronyl Radical‐Catalyzed (4+2) Cycloaddition | ACIE |
33 | Rhodium‐Catalyzed Asymmetric Cyclopropanation of Indoles with N‐Triftosylhydrazones | ACIE |
34 | Ring Contraction of Saturated Cyclic Amines and Rearrangement of Acyclic Amines Through Their Corresponding Hydroxylamines | ACIE |
35 | Second Generation Catalytic Enantioselective Nucleophilic Desymmetrization at Phosphorus (V): Improved Generality, Efficiency and Modularity | ACIE |
36 | Selective Cross‐Metathesis Versus Ring‐Closing Metathesis of Terpenes, Taking the Path Less Travelled | ACIE |
37 | Site‐Selective Activation and Stereospecific Functionalization of Bis(boronic Esters) Derived from 2‐Alkenes: Construction of Propionates and Other 1,2‐Difunctional Motifs | ACIE |
38 | Site‐Specific Deaminative Trifluoromethylation of Aliphatic Primary Amines** | ACIE |
39 | Site‐selective Photoredox‐Catalyzed Late‐stage Benzylic Hydrogen Isotope Exchange | ACIE |
40 | Skeletal Editing of Aromatic N‐Heterocycles via Hydroborative Cleavage of C−N Bonds—Scope, Mechanism, and Property | ACIE |
41 | Spiro[3.3]heptane as a Saturated Benzene Bioisostere** | ACIE |
42 | Stereodivergency in Copper‐Catalyzed Borylative Difunctionalizations: The Impact of Boron Coordination | ACIE |
43 | Stereoselective Copper‐Catalyzed Olefination of Imines | ACIE |
44 | Stereoselective C−B and C−H Bonds Functionalization of PolyBorylated Alkenes | ACIE |
45 | Streamlining the Synthesis of Pyridones through Oxidative Amination of Cyclopentenones | ACIE |
46 | Sulfonium Rearrangements Enable the Direct Preparation of Sulfenyl Imidinium Salts | ACIE |
47 | The Synthesis and Reactivity of Naphthoquinonynes | ACIE |
48 | Total Synthesis of Lissodendoric Acid A | ACIE |
49 | Traceless Nucleophile Strategy for C5‐Selective C−H Sulfonylation of Pyridines | ACIE |
50 | Unlocking the Asymmetric Hydrogenation of Tetrasubstituted Acyclic Enones | ACIE |
51 | Vitamin B12‐Photocatalyzed Cyclopropanation of Electron‐Deficient Alkenes Using Dichloromethane as the Methylene Source** | ACIE |
52 | Werner Salt as Nickel and Ammonia Source for Photochemical Synthesis of Primary Aryl Amines | ACIE |
53 | Acid-Catalyzed Oxy-aminomethylation of Styrenes | ACS Catal. |
54 | Cross-Coupling Reactions with Nickel, Visible Light, and tert-Butylamine as a Bifunctional Additive | ACS Catal. |
55 | Intermolecular Anti-Markovnikov Hydroamination of Alkenes with Sulfonamides, Sulfamides, and Sulfamates | ACS Catal. |
56 | Recent Advances in Catalytic Nitrogen–Nitrogen Bond Formation Reactions | ACS Catal. |
57 | Reductive Olefin Bicyclo[1.1.0]butane Coupling Enabled by Iron Hydride Hydrogen Atom Transfer | ACS Catal. |
58 | Ti-Catalyzed Oxidative Amination Using Anilines | ACS Catal. |
59 | Selective 1,4-syn-Addition to Cyclic 1,3-Dienes via Hybrid Palladium Catalysis | ACS Central Science |
60 | Visible Light instead of Transition Metal: Electron Donor Acceptor Complex Enabled Cross‐Coupling of Aryl Halides with Active Methylene Compounds | Adv. Synth. Catal. |
61 | Aluminium porphyrins catalyse the hydrogenation of CO2 with H2 | Chem. Sci. |
62 | Boryl radical-mediated halogen-atom transfer (XAT) enables the Sonogashira-like alkynylation of alkyl halides | Chem. Sci. |
63 | Exploring the molecular design principles for efficient diarylethene photoacid and photohydride generators based on the photochemical reaction mechanism | Chem. Sci. |
64 | Nitrogen atom insertion into arenols to access benzazepines | Chem. Sci. |
65 | Photocatalytic (3 + 2) dipolar cycloadditions of aziridines driven by visible-light | Chem. Sci. |
66 | Photocatalytic, modular difunctionalization of alkenes enabled by ligand-to-metal charge transfer and radical ligand transfer | Chem. Sci. |
67 | Transfer learning for a foundational chemistry model | Chem. Sci. |
68 | Anti-selective Cyclopropanation of Nonconjugated Alkenes with Diverse Pronucleophiles via Directed Nucleopalladation | JACS |
69 | 14N to 15N Isotopic Exchange of Nitrogen Heteroaromatics through Skeletal Editing | JACS |
70 | 15NRORC: An Azine Labeling Protocol | JACS |
71 | A Bimolecular Homolytic Substitution-Enabled Platform for Multicomponent Cross-Coupling of Unactivated Alkenes | JACS |
72 | A Dual Cobalt and Photoredox Catalysis for Hydrohalogenation of Alkenes | JACS |
73 | A General Platform for Visible Light Sulfonylation Reactions Enabled by Catalytic Triarylamine EDA Complexes | JACS |
74 | A General Strategy for N-(Hetero)arylpiperidine Synthesis Using Zincke Imine Intermediates | JACS |
75 | A General Synthetic Strategy toward the Truxillate Natural Products via Solid-State Photocycloadditions | JACS |
76 | A Modular Strategy for the Synthesis of Macrocycles and Medium-Sized Rings via Cyclization/Ring Expansion Cascade Reactions | JACS |
77 | A Radical Strategy for the Alkylation of Amides with Alkyl Halides by Merging Boryl Radical-Mediated Halogen-Atom Transfer and Copper Catalysis | JACS |
78 | A Strain-Promoted Divergent Chemical Steroidation Unveils Potent Anti- Inflammatory Pseudo-Steroidal Glycosides | JACS |
79 | A Type of Chiral C2-Symmetric Arylthiol Catalyst for Highly Enantioselective Anti-Markovnikov Hydroamination | JACS |
80 | Alkene Hydrobenzylation by a Single Catalyst That Mediates Iterative Outer-Sphere Steps | JACS |
81 | Alkoxy Radical Generation Mediated by Sulfoxide Cation Radicals for Alcohol-Directed Aliphatic C–H Functionalization | JACS |
82 | Alkynes to (Free) Carbenes to Polycyclic Cyclopropanes | JACS |
83 | An Azide-Free Synthesis of Metallodiazomethanes Using Nitrous Oxide | JACS |
84 | Aziridine Group Transfer via Transient N-Aziridinyl Radicals | JACS |
85 | Bicyclo[2.2.0]hexene: A Multicyclic Mechanophore with Reactivity Diversified by External Forces | JACS |
86 | Borane-Catalyzed Enantioselective α-Alkylation of Unactivated 2-Alkylbenzoxazoles with Electron-Deficient Olefins | JACS |
87 | C3 Selective Hydroxylation of Pyridines via Photochemical Valence Isomerization of Pyridine N-Oxides | JACS |
88 | Carboiodanation of Arynes: Organoiodine(III) Compounds as Nucleophilic Organometalloids | JACS |
89 | Catalytic Asymmetric Barbier Reaction of Ketones with Unactivated Alkyl Electrophiles | JACS |
90 | Catalytic Asymmetric Construction of Chiral Polysubstituted 3-Azabicyclo[3.1.1]heptanes by Copper-Catalyzed Stereoselective Formal [4π+2σ] Cycloaddition | JACS |
91 | Catalytic Asymmetric Cycloaddition of Olefins with In Situ Generated N-Boc-Formaldimine | JACS |
92 | Catalytic Enantioselective Nucleophilic α-Chlorination of Ketones with NaCl | JACS |
93 | Catalytic Intermolecular Deoxygenative Coupling of Carbonyl Compounds with Alkynes by a Cp*Mo(II)-Catalyst | JACS |
94 | Catalytic Regio- and Enantioselective Boracarboxylation of Arylalkenes with CO2 and Diboron | JACS |
95 | Chemoselective Diazine Dearomatization: The Catalytic Enantioselective Dearomatization of Pyrazine | JACS |
96 | Chiral Brønsted Acid-Catalyzed Intramolecular Asymmetric Dearomatization Reaction of Indoles with Cyclobutanones via Cascade Friedel–Crafts/Semipinacol Rearrangement | JACS |
97 | Cobalt-Catalyzed Asymmetric Hydrogenation of Ketones Enabled by the Synergism of an N–H Functionality and a Redox-Active Ligand | JACS |
98 | Computational Design of Ligands for the Ir-Catalyzed C5-Borylation of Indoles through Tuning Dispersion Interactions | JACS |
99 | Computational Methods Enable the Prediction of Improved Catalysts for Nickel-Catalyzed Cross-Electrophile Coupling | JACS |
100 | Computationally Guided Ligand Discovery from Compound Libraries and Discovery of a New Class of Ligands for Ni-Catalyzed Cross- Electrophile Coupling of Challenging Quinoline Halides | JACS |
101 | Construction of Vicinal Quaternary Centers via Ru-Catalyzed Enantiospecific Allylic Substitution with Lithium Ester Enolates | JACS |
102 | Cooperative Phosphine-Photoredox Catalysis Enables N–H Activation of Azoles for Intermolecular Olefin Hydroamination | JACS |
103 | Copper(I)-Catalyzed Enantioselective α-Alkylation of 2-Acylimidazoles | JACS |
104 | Copper-Catalyzed Amination of Aryl Chlorides under Mild Reaction Conditions | JACS |
105 | Copper–Nitroxyl-Catalyzed α-Oxygenation of Cyclic Secondary Amines Including Application to Late-Stage Functionalization | JACS |
106 | Cyclopropanation with Non-Stabilized Carbenes via Ketyl Radicals | JACS |
107 | Dearomatization of Pyridines: Photochemical Skeletal Enlargement for the Synthesis of 1,2-Diazepines | JACS |
108 | Development of a Deactivation-Resistant Dialkylbiarylphosphine Ligand for Pd-Catalyzed Arylation of Secondary Amines | JACS |
109 | Development of a General Organophosphorus Radical Trap: Deoxyphosphonylation of Alcohols | JACS |
110 | Difluorocarbene Generation via a Spin-Forbidden Excitation under Visible Light Irradiation | JACS |
111 | Direct Bioisostere Replacement Enabled by Metallaphotoredox Deoxydifluoromethylation | JACS |
112 | Direct C–H Hydroxylation of N-Heteroarenes and Benzenes via Base-Catalyzed Halogen Transfer | JACS |
113 | Direct Enantioselective α-C–H Conjugate Addition of Propargylamines to α,β-Unsaturated Ketones via Carbonyl Catalysis | JACS |
114 | Divergent Synthesis of Scabrolide A and Havellockate via an exo-exo-endo Radical Cascade | JACS |
115 | Double Strain-Release [2π+2σ]-Photocycloaddition | JACS |
116 | Dual Ligand Enabled Pd-Catalyzed Ortho-Alkylation of Iodoarenes | JACS |
117 | Electrochemistry-Enabled C-Heteroatom Bond Formation of Alkyl Germanes | JACS |
118 | Enantioselective Alkylation of Primary C(sp3)–H Bonds in N-Methyl Tertiary Amine Enabled by Iridium Complex of Axially Chiral β-Aryl Porphyrins | JACS |
119 | Enantioselective Aziridination of Unactivated Terminal Alkenes Using a Planar Chiral Rh(III) Indenyl Catalyst | JACS |
120 | Enantioselective Carbon Isotope Exchange | JACS |
121 | Enantioselective Carbonylative Cyclization of Alkenes with C–H Bonds for Synthesis of γ-Lactams Bearing an α-Quaternary Carbon | JACS |
122 | Enantioselective Nickel-Electrocatalyzed Cross-Dehydrogenative α- and γ-Nitroalkylation | JACS |
123 | Enantioselective Potassium-Catalyzed Wittig Olefinations | JACS |
124 | Fe/Thiol Cooperative Hydrogen Atom Transfer Olefin Hydrogenation: Mechanistic Insights That Inform Enantioselective Catalysis | JACS |
125 | Formal meta-C–H-Fluorination of Pyridines and Isoquinolines through Dearomatized Oxazinopyridine Intermediates | JACS |
126 | Formal [2σ + 2σ]-Cycloaddition of Aziridines with Bicyclo[1.1.0]butanes: Access to Enantiopure 2-Azabicyclo[3.1.1]heptane Derivatives | JACS |
127 | From Methane to Methanol: Pd-iC-CeO2 Catalysts Engineered for High Selectivity via Mechanochemical Synthesis | JACS |
128 | General Installation of (4H)-Imidazolone cis-Amide Bioisosteres Along the Peptide Backbone | JACS |
129 | General Regio- and Diastereoselective Allylic C–H Oxygenation of Internal Alkenes | JACS |
130 | Generality-Driven Catalyst Development: A Universal Catalyst for Enantioselective Nitroalkene Reduction | JACS |
131 | Harnessing Oxetane and Azetidine Sulfonyl Fluorides for Opportunities in Drug Discovery | JACS |
132 | Incorporating Synthetic Accessibility in Drug Design: Predicting Reaction Yields of Suzuki Cross-Couplings by Leveraging AbbVie’s 15-Year Parallel Library Data Set | JACS |
133 | Iridium-Catalyzed Enantioconvergent Construction of Piperidines and Tetrahydroisoquinolines from Racemic 1,5-Diols | JACS |
134 | Iron-Catalyzed Cross-Electrophile Coupling for the Formation of All- Carbon Quaternary Centers | JACS |
135 | Iron-Catalyzed Primary Amination of C(sp3)–H Bonds | JACS |
136 | Iterative Catalyst-Controlled Diastereoselective Matteson Homologations Enable the Selective Synthesis of Benzestrol Isomers | JACS |
137 | Iterative One-Carbon Homologation of Unmodified Carboxylic Acids | JACS |
138 | Kinetic Modeling Enables Understanding of Off-Cycle Processes in Pd- Catalyzed Amination of Five-Membered Heteroaryl Halides | JACS |
139 | Late-Stage Saturation of Drug Molecules | JACS |
140 | Ligand-Controlled Cobalt-Catalyzed Regio-, Enantio-, and Diastereoselective Oxyheterocyclic Alkene Hydroalkylation | JACS |
141 | Mechanistic Investigation, Wavelength-Dependent Reactivity, and Expanded Reactivity of N–Aryl Azacycle Photomediated Ring Contractions | JACS |
142 | Merging Organocatalysis with 1,2-Boronate Rearrangement: A Lewis Base- Catalyzed Asymmetric Multicomponent Reaction | JACS |
143 | Metallomimetic C–F Activation Catalysis by Simple Phosphines | JACS |
144 | Modular Access to Functionalized Oxetanes as Benzoyl Bioisosteres | JACS |
145 | Modular, Enantioselective Entry into Polysubstituted Shapeshifting Molecules | JACS |
146 | Multicomponent Construction of Tertiary Alkylamines by Photoredox/Nickel-Catalyzed Aminoalkylation of Organohalides | JACS |
147 | Multicomponent Synthesis of α-Branched Amines via a Zinc-Mediated Carbonyl Alkylative Amination Reaction | JACS |
148 | Multielectron Reduction of Esters by a Diazabenzacenaphthenium Photoredox Catalyst | JACS |
149 | Multifunctionalization of Alkenyl Alcohols via a Sequential Relay Process | JACS |
150 | Ni-Catalyzed Asymmetric Reductive Arylation of α-Substituted Imides | JACS |
151 | Nickel-Catalyzed Carbonylative Negishi Cross-Coupling of Unactivated Secondary Alkyl Electrophiles with 1 atm CO Gas | JACS |
152 | Nickel-Catalyzed Enantioselective C(sp3)–C(sp3) Cross-Electrophile Coupling of N-Sulfonyl Styrenyl Aziridines with Alkyl Bromides | JACS |
153 | Nickel-Catalyzed Hydrofluorination in Unactivated Alkenes: Regio- and Enantioselective C–F Bond Formation | JACS |
154 | Non-Innocent Role of Sacrificial Anodes in Electrochemical Nickel- Catalyzed C(sp2)–C(sp3) Cross-Electrophile Coupling | JACS |
155 | Oxidative Dearomatization of Pyridines | JACS |
156 | Oxidative Nitrogen Insertion into Silyl Enol Ether C═C Bonds | JACS |
157 | Oxoammonium-Catalyzed Oxidation of N-Substituted Amines | JACS |
158 | Palladium-Catalyzed Amination of Aryl Halides with Aqueous Ammonia and Hydroxide Base Enabled by Ligand Development | JACS |
159 | Pd/Cu-Cocatalyzed Enantio- and Diastereodivergent Wacker-Type Dicarbofunctionalization of Unactivated Alkenes | JACS |
160 | Photoredox Nucleophilic (Radio)fluorination of Alkoxyamines | JACS |
161 | Practical Synthesis of Chiral α-Aminophosphonates with Weak Bonding Organocatalysis at ppm Loading | JACS |
162 | Programmable Piperazine Synthesis via Organic Photoredox Catalysis | JACS |
163 | Radical Replacement Process for Ligated Boryl Radical-Mediated Activation of Unactivated Alkyl Chlorides for C(sp3)–C(sp3) Bond Formation | JACS |
164 | Rapid Exploration of Chemical Space by High-Throughput Desorption Electrospray Ionization Mass Spectrometry | JACS |
165 | Red Light–Blue Light Chromoselective C(sp2)–X Bond Activation by Organic Helicenium-Based Photocatalysis | JACS |
166 | Redox-Neutral, Iron-Mediated Directed C–H Activation: General Principles and Mechanistic Insights | JACS |
167 | Reductive Cyclopropanation through Bismuth Photocatalysis | JACS |
168 | Regiodivergent Ring-Expansion of Oxindoles to Quinolinones | JACS |
169 | Regioselective Pyridine to Benzene Edit Inspired by Water-Displacement | JACS |
170 | Remote C–H Amination and Alkylation of Camphor at C8 through Hydrogen- Atom Abstraction | JACS |
171 | Rhodium-Catalyzed Asymmetric Reductive Hydroformylation of α-Substituted Enamides | JACS |
172 | Silyl Radicals as Single-Electron Reductants: α-Aminoalkyl Radical Formation via a Photocatalytic Oxidatively Initiated Radical Chain Process | JACS |
173 | Simplified Modular Access to Enantiopure 1,2-Aminoalcohols via Ni- Electrocatalytic Decarboxylative Arylation | JACS |
174 | Simultaneous Stereoinvertive and Stereoselective C(sp3)–C(sp3) Cross-Coupling of Boronic Esters and Allylic Carbonates | JACS |
175 | Stereodivergent Synthesis of 1,4-Dicarbonyl Compounds through Sulfonium Rearrangement: Mechanistic Investigation, Stereocontrolled Access to γ-Lactones and γ-Lactams, and Total Synthesis of Paraconic Acids | JACS |
176 | Stereospecific Phosphination and Thioetherification of Organoboronic Esters | JACS |
177 | Sustainable Aerobic Allylic C–H Bond Oxidation with Heterogeneous Iron Catalyst | JACS |
178 | Switchable Decarboxylation by Energy- or Electron-Transfer Photocatalysis | JACS |
179 | Switchable and Chemoselective Arene Hydrogenation for Efficient Late Stage Applications | JACS |
180 | Synthesis and Suzuki–Miyaura Cross-Coupling of Alkyl Amine-Boranes. A Boryl Radical-Enabled Strategy | JACS |
181 | Synthesis of 15N-Pyridines and Higher Mass Isotopologs via Zincke Imine Intermediates | JACS |
182 | Total Synthesis Facilitates In Vitro Reconstitution of the C–S Bond-Forming P450 in Griseoviridin Biosynthesis | JACS |
183 | Total Synthesis of Putative Melognine | JACS |
184 | Versatile, Modular, and General Strategy for the Synthesis of α-Amino Carbonyls | JACS |
185 | Vinyltriarylbismuthonium Salts: Powerful Vehicles for α-Vinylation of Carbonyl Compounds | JACS |
186 | Visible-Light Photocatalytic C–H Amination of Arenes Utilizing Acridine–Lewis Acid Complexes | JACS |
187 | Visible-Light-Mediated Vicinal Dihalogenation of Unsaturated C–C Bonds Using Dual-Functional Group Transfer Reagents | JACS |
188 | Discovery of Nelutroctiv (CK-136), a Selective Cardiac Troponin Activator for the Treatment of Cardiovascular Diseases Associated with Reduced Cardiac Contractility | JMC |
189 | Fentanyl-Type Antagonist of the μ-Opioid Receptor: Important Role of Axial Chirality in the Active Conformation | JMC |
190 | MicroCycle: An Integrated and Automated Platform to Accelerate Drug Discovery | JMC |
191 | A 21st Century View of Allowed and Forbidden Electrocyclic Reactions | JOC |
192 | Accessing Highly Substituted Indoles via B(C6F5)3-Catalyzed Secondary Alkyl Group Transfer | JOC |
193 | Construction of Seven-Membered Oxacycles Using a Rh(I)-Catalyzed Cascade C–C Formation/Cleavage of Cyclobutenol Derivatives | JOC |
194 | Metal-Free Synthesis of 4-Bromoisoquinolines through Brominative Annulation of 2-Alkynyl Arylimidate Using In Situ-Generated Transient Bromoiodane | JOC |
195 | Organocatalytic Decarboxylative Borylation of Cyclopropane N-Hydroxyphthalimide Esters | JOC |
196 | Oxygenation of Phenols with Water as the Oxygen Source and Oxoammonium Salt as the Oxidant | JOC |
197 | Photocatalyzed Amination of Alkyl Halides to Access Primary Amines | JOC |
198 | Ring Opening of N-Acyl Lactams Using Nickel-Catalyzed Transamidation | JOC |
199 | Visible Light Mediated Chemoselective Hydroxylation of Benzylic Methylenes | JOC |
200 | α-Acyloxylation of Ketones/Cyclic Ethers Mediated by Hypervalent Iodine(III) Reagents as Oxidants and Nucleophilic Sources | JOC |
201 | C–heteroatom coupling with electron-rich aryls enabled by nickel catalysis and light | Nat. Cat. |
202 | Nickel-catalysed enantioselective alkene dicarbofunctionalization enabled by photochemical aliphatic C–H bond activation | Nat. Cat. |
203 | Nickel-electrocatalysed C(sp3)–C(sp3) cross-coupling of unactivated alkyl halides | Nat. Cat. |
204 | Photocatalytic generation of alkyl carbanions from aryl alkenes | Nat. Cat. |
205 | Photoredox-catalysed amidyl radical insertion to bicyclo[1.1.0]butanes | Nat. Cat. |
206 | Radical strain-release photocatalysis for the synthesis of azetidines | Nat. Cat. |
207 | Ring expansion of indene by photoredox-enabled functionalized carbon- atom insertion | Nat. Cat. |
208 | The iron-catalysed Suzuki coupling of aryl chlorides | Nat. Cat. |
209 | A general copper-catalysed enantioconvergent C(sp3)–S cross-coupling via biomimetic radical homolytic substitution | Nat. Chem. |
210 | A para- to meta-isomerization of phenols | Nat. Chem. |
211 | Asymmetric dearomative single-atom skeletal editing of indoles and pyrroles | Nat. Chem. |
212 | Bridging the information gap in organic chemical reactions | Nat. Chem. |
213 | Carbonyl cross-metathesis via deoxygenative gem-di-metal catalysis | Nat. Chem. |
214 | Cobalt-catalysed desymmetrization of malononitriles via enantioselective borohydride reduction | Nat. Chem. |
215 | Discovery of N–X anomeric amides as electrophilic halogenation reagents | Nat. Chem. |
216 | Diversified ring expansion of saturated cyclic amines enabled by azlactone insertion | Nat. Chem. |
217 | Dynamic amine sorting enables multiselective construction of unsymmetrical chiral diamines | Nat. Chem. |
218 | Enantioselective construction of stereogenic-at-sulfur(IV) centres via catalytic acyl transfer sulfinylation | Nat. Chem. |
219 | Enantiospecific cross-coupling of cyclic alkyl sulfones | Nat. Chem. |
220 | Engineering a nanoscale liposome-in-liposome for in situ biochemical synthesis and multi-stage release | Nat. Chem. |
221 | Gold-catalysed amine synthesis by reductive hydroamination of alkynes with nitroarenes | Nat. Chem. |
222 | Modular alkene synthesis from carboxylic acids, alcohols and alkanes via integrated photocatalysis | Nat. Chem. |
223 | Modular chemoenzymatic synthesis of ten fusicoccane diterpenoids | Nat. Chem. |
224 | Modular enantioselective assembly of multi-substituted boron- stereogenic BODIPYs | Nat. Chem. |
225 | Modular α-tertiary amino ester synthesis through cobalt-catalysed asymmetric aza-Barbier reaction | Nat. Chem. |
226 | Probing the chemical ‘reactome’ with high-throughput experimentation data | Nat. Chem. |
227 | Programmable late-stage functionalization of bridge-substituted bicyclo[1.1.1]pentane bis-boronates | Nat. Chem. |
228 | Radical-triggered translocation of C–C double bond and functional group | Nat. Chem. |
229 | Repurposing of halogenated organic pollutants via alkyl bromide- catalysed transfer chlorination | Nat. Chem. |
230 | Synthesis of polysubstituted azepanes by dearomative ring expansion of nitroarenes | Nat. Chem. |
231 | Triazenolysis of alkenes as an aza version of ozonolysis | Nat. Chem. |
232 | Triplet carbenes with transition-metal substituents | Nat. Chem. |
233 | Tunable molecular editing of indoles with fluoroalkyl carbenes | Nat. Chem. |
234 | Generation and reactivity of unsymmetrical strained heterocyclic allenes | Nat. Synth. |
235 | Synthesis of alkenyl boronates through stereoselective vinylene homologation of organoboronates | Nat. Synth. |
236 | Visible-light-driven synthesis of N-heteroaromatic carboxylic acids by thiolate-catalysed carboxylation of C(sp²)–H bonds using CO2 | Nat. Synth. |
237 | A Gram-negative-selective antibiotic that spares the gut microbiome | Nature |
238 | A deconstruction–reconstruction strategy for pyrimidine diversification | Nature |
239 | A general strategy for the synthesis of taxane diterpenes | Nature |
240 | A light-driven enzymatic enantioselective radical acylation | Nature |
241 | Alkene dialkylation by triple radical sorting | Nature |
242 | Asymmetric hydrogenation of ketimines with minimally different alkyl groups | Nature |
243 | Boron catalysis in a designer enzyme | Nature |
244 | Catalysis of an SN2 pathway by geometric preorganization | Nature |
245 | Catalytic asymmetric cationic shifts of aliphatic hydrocarbons | Nature |
246 | Catalytic glycosylation for minimally protected donors and acceptors | Nature |
247 | Computational prediction of complex cationic rearrangement outcomes | Nature |
248 | Continuous collective analysis of chemical reactions | Nature |
249 | Copper-catalysed dehydrogenation or lactonization of C(sp3)–H bonds | Nature |
250 | Couple-close construction of polycyclic rings from diradicals | Nature |
251 | Coupling of unactivated alkyl electrophiles using frustrated ion pairs | Nature |
252 | Direct radical functionalization of native sugars | Nature |
253 | Dynamic stereomutation of vinylcyclopropanes with metalloradicals | Nature |
254 | Electrocatalytic reductive deuteration of arenes and heteroarenes | Nature |
255 | Emergence of a distinct mechanism of C–N bond formation in photoenzymes | Nature |
256 | Hydroamination of alkenes with dinitrogen and titanium polyhydrides | Nature |
257 | Identifying general reaction conditions by bandit optimization | Nature |
258 | Photocatalytic C–F bond activation in small molecules and polyfluoroalkyl substances | Nature |
259 | Reductive alkyl–alkyl coupling from isolable nickel–alkyl complexes | Nature |
260 | Stereoselective amino acid synthesis by photobiocatalytic oxidative coupling | Nature |
261 | Stereospecific alkenylidene homologation of organoboronates by SNV reaction | Nature |
262 | Stereospecific radical coupling with a non-natural photodecarboxylase | Nature |
263 | Symmetry breaking and chiral amplification in prebiotic ligation reactions | Nature |
264 | Synergistic photobiocatalysis for enantioselective triple-radical sorting | Nature |
265 | Synthesis of non-canonical amino acids through dehydrogenative tailoring | Nature |
266 | Unimolecular net heterolysis of symmetric and homopolar σ-bonds | Nature |
267 | Unlocking carbene reactivity by metallaphotoredox α-elimination | Nature |
268 | Asymmetric Synthesis of the cis-1,2-Diaryltetralin Vepdegestrant Core via an Enantioselective Intramolecular Corey- Chaykovsky Epoxidation | OPRD |
269 | Enabling Data-Driven Solubility Modeling at GSK: Enhancing Purge Predictions for Mutagenic Impurities | OPRD |
270 | G-EnzyBeads for Biocatalysis Screening Facilitated by Volumetric Dosing | OPRD |
271 | Optimization and Scale-Up Synthesis of a Lappaconitine Alkaloid Derivative, QG3030, as a Novel Osteoanabolic Agent | OPRD |
272 | Oxygen-, Nitrogen-, and Sulfur-Containing Heterocycles: Recent Advances in De Novo Synthesis and Prospect | OPRD |
273 | Practical and Efficient Approach to Scalable Synthesis of Rucaparib | OPRD |
274 | Process Development for the Manufacture of a Topical Pan-Trk Inhibitor Incorporating Decarboxylative sp2–sp3 Cross- Coupling | OPRD |
275 | Process Development to Synthesize SGD-11275 Utilizing a Pd-Catalyzed Acetamide Arylation and Gallium-Mediated Friedel–Crafts Acylation | OPRD |
276 | Veliparib: Analytical Tools and Process Design Strategies for the Control of Mutagenic Impurities and Other Drug Substance Critical Quality Attributes | OPRD |
277 | N-Oxide-to-Carbon Transmutations of Azaarene N-Oxides | Org. Lett. |
278 | Assembly of 2-Substituted Tetrahydroquinolines from ortho-Methylbenzenesulfamides and Dienes, Using a C(sp3)–H Activation/Annulation Sequence | Org. Lett. |
279 | C(sp3)–C(sp3) Coupling of Cycloalkanes and Alkyl Halides via Dual Photocatalytic Hydrogen Atom Transfer and Nickel Catalysis | Org. Lett. |
280 | Catalytic Generation of Pyridyl Radicals via Electron Donor–Acceptor Complex Photoexcitation: Synthesis of 2-Pyridylindole-Based Heterobiaryls | Org. Lett. |
281 | Decarboxylative Nucleophilic Fluorination of Aliphatic Carboxylic Acids | Org. Lett. |
282 | Diazene-Catalyzed Oxidative Alkyl Halide–Olefin Metathesis | Org. Lett. |
283 | Dual Function of N-Iodosuccinimide for C(sp3)–B Bond Activation | Org. Lett. |
284 | General Approach to Amides through Decarboxylative Radical Cross- Coupling of Carboxylic Acids and Isocyanides | Org. Lett. |
285 | Ground State Generation and Cyclization of Aminium Radicals in the Formation of Tetrahydroquinolines | Org. Lett. |
286 | Ligand-Controlled On–Off Switch of a Silicon-Tethered Directing Group Enabling the Regiodivergent Hydroalkylation of Vinylsilanes under Ni–H Catalysis | Org. Lett. |
287 | Nickel-Catalyzed Deoxygenative Amidation of Alcohols with Carbamoyl Chlorides | Org. Lett. |
288 | Photochemical Reduction of Quinolines with γ-Terpinene | Org. Lett. |
289 | Photoredox/Nickel Dual Catalysis-Enabled Aryl Formylation with 2,2-Dimethoxy-N,N-dimethylethan-1-amine as CO Source | Org. Lett. |
290 | Radical versus Non-Radical Reactivity in ortho- and para-Quinonedimethides and Implications for Cycloaddition Mechanisms | Org. Lett. |
291 | Redefining the Synthetic Logic of Medicinal Chemistry. Photoredox- Catalyzed Reactions as a General Tool for Aliphatic Core Functionalization | Org. Lett. |
292 | Rhodium-Catalyzed Double Dearomatization of 1,2,3-Triazole–Isoxazole Dyads: Synthesis of Nonfused 1H-1,3-Diazepines | Org. Lett. |
293 | Ti(III)-Catalyzed Anti-Markovnikov Reduction of Epoxides with Borohydride | Org. Lett. |
294 | Visible-Light-Promoted α-C(sp3)–H Amination of Ethers with Azoles and Amides | Org. Lett. |
295 | A decarbonylative approach to alkylnickel intermediates and C(sp 3 )-C(sp 3 ) bond formation | Science |
296 | A solid noncovalent organic double-helix framework catalyzes asymmetric [6 + 4] cycloaddition | Science |
297 | A solution to the anti-Bredt olefin synthesis problem | Science |
298 | Alcohol-alcohol cross-coupling enabled by S H 2 radical sorting | Science |
299 | AlphaFold2 structures guide prospective ligand discovery | Science |
300 | Aminative Suzuki–Miyaura coupling | Science |
301 | An oxidative photocyclization approach to the synthesis of Securiflustra securifrons alkaloids | Science |
302 | Asymmetric photoenzymatic incorporation of fluorinated motifs into olefins | Science |
303 | Binding and sensing diverse small molecules using shape-complementary pseudocycles | Science |
304 | Biocatalytic C–H oxidation meets radical cross-coupling: Simplifying complex piperidine synthesis | Science |
305 | Carbon quaternization of redox active esters and olefins by decarboxylative coupling | Science |
306 | Catalytic enantioselective reductive Eschenmoser-Claisen rearrangements | Science |
307 | Cobalt-catalyzed synthesis of amides from alkenes and amines promoted by light | Science |
308 | Differentiating enantiomers by directional rotation of ions in a mass spectrometer | Science |
309 | Direct propylene epoxidation via water activation over Pd-Pt electrocatalysts | Science |
310 | Enantioselective remote methylene C−H (hetero)arylation of cycloalkane carboxylic acids | Science |
311 | Expansive discovery of chemically diverse structured macrocyclic oligoamides | Science |
312 | Highly pure DNA-encoded chemical libraries by dual-linker solid-phase synthesis | Science |
313 | Nickel binding enables isolation and reactivity of previously inaccessible 7-aza-2,3-indolynes | Science |
314 | Nitrate reduction enables safer aryldiazonium chemistry | Science |
315 | Ph 3 PCN 2 : A stable reagent for carbon-atom transfer | Science |
316 | Photocatalytic furan-to-pyrrole conversion | Science |
317 | Photochemical phosphorus-enabled scaffold remodeling of carboxylic acids | Science |
318 | Photosensitization enables Pauson-Khand–type reactions with nitrenes | Science |
319 | Radical-mediated click-clip reactions | Science |
320 | Stereodivergent access to non-natural α-amino acids via enantio- and Z / E -selective catalysis | Science |
321 | Sulfenylnitrene-mediated nitrogen-atom insertion for late-stage skeletal editing of N -heterocycles | Science |
322 | Synchronous recognition of amines in oxidative carbonylation toward unsymmetrical ureas | Science |
323 | Targeting cancer with small-molecule pan-KRAS degraders | Science |
324 | Terminal C(sp 3 )–H borylation through intermolecular radical sampling | Science |
325 | The sugar cube: Network control and emergence in stereoediting reactions | Science |
326 | Total synthesis of (−)-cylindrocyclophane A facilitated by C−H functionalization | Science |
327 | Visible light–mediated aza Paternò–Büchi reaction of acyclic oximes and alkenes to azetidines | Science |