|
Ruthenium-Catalyzed [4 + 2] Cycloaddition of Chromanone Dienes Using Triethylamine as an Ethylene Surrogate
|
1.00 |
|
Ru-Catalyzed Additive-Controlled Spirocyclization/Alkenylation of Benzimidates with 1,4-Naphthoquinone
|
1.00 |
|
Photocatalytic Deacylative 1,2-Alkyl(hetero)arylation of Electron-Rich Styrenes
|
1.00 |
|
Photochemical Switchable Access to Spiro-γ-lactams and Spiro-γ-lactones from Olefins via a N to O Atom Swap
|
1.00 |
|
Iterative C–H Amidation of Thiophenes under High-Valent Cp*Co(III) Catalysis
|
1.00 |
|
Cobalt-Catalyzed Asymmetric Annulative Dienylation with Allenyl Carbinol Acetates via Desymmetrization
|
1.00 |
|
Co/Salox-Catalyzed Enantioselective C–H Annulation for One-Step Generation of C–N Axial and C Central Chirality
|
0.67 |
|
Nickel-Catalyzed Regio- and Stereoselective Alkylation and Dimerization of Allenes: Harnessing the Flexibility of Nickel Oxidation States in Reductive Allene Coupling
|
1.00 |
|
Modular Synthesis of Triaroyl Cyclopropanes via a Formal Cyclotrimerization of Phenacyl Bromides and Their Transformation into Diazabicycles
|
1.00 |
|
Rh-Catalyzed Cascade C–H Functionalization/Aromatization of Benzylamines with Vinylcyclopropanes: Access to Functionalized Isoquinolines
|
1.00 |
|
Copper-Catalyzed Selective Mononitration of Unbiased ortho-C–H Bonds in Arenes Using a Ball Mill in Air: Excellent Compatibility with Heterocycles
|
1.00 |
|
Unified Photoredox Platform for Divergent SO2‑Capture Transformations: Substrate-Controlled Switch toward 1,4-HAT-Enabled 1,2-Hydrosulfonylation or 1,2-Sulfonylative Spirolactamization
|
1.00 |
|
Cascade Reaction of α, β-Unsaturated Keto-carboxylic Acid for the Formation of 5-Substituted Isoxazole using NaN3/I2/TBHP
|
1.00 |
|
Electron Donor–Acceptor Complex-Enabled Remote 1,n-Difunctionalization of Alkenes via Distal C(sp3)–H Activation
|
1.00 |
|
Pd-Catalyzed Tandem Synthesis of Polysubstituted Pyridines Using β-Enamino Esters and β-Ketodinitriles
|
1.00 |
|
Light-Driven EDA–APEX Approach: A One-Pot Access to Phenanthrenes and Naphthalenes
|
1.00 |
|
Progressive Chemoselective Reductive Deuteration and Deuterodefluorination of Fluoroalkyl Ketones Using D2O
|
0.75 |
|
A Multicomponent Approach for the Synthesis of Indeno-Pyrrolido-Pyrimidino-Azoles: Access to Structurally Diverse Pseudo-Natural Products
|
1.00 |
|
Higher-Order [10 + 2] Annulation Strategy for the Synthesis of CF3-Functionalized Benzopentalenes
|
1.00 |
|
Total Synthesis of Annonaceae Acetogenins Calamistrin A and Uvarigrin
|
1.00 |
|
N-Heterocyclic Carbene-Catalyzed Aza-Benzoin–Michael Addition–Lactamization Cascade Incorporating a Formal [4 + 1] Annulation to Access Tricyclic Indeno[2,1-b]pyrrole Derivatives
|
1.00 |
|
Asymmetric Organocatalytic (4 + 4) Annulation between 5-Alkenyl Thiazolones and α,β-Ynones: Access to Thiazole-Fused Eight-Membered Cyclic Ethers
|
1.00 |
|
Metallo Protic N-Allyl Enammonium Ylide 3-Aza-Cope Rearrangement Enabled by Resonance-Assisted H-Bonding: Direct Access to Functionalized Pyrroles
|
1.00 |
|
Intramolecular Alder-Ene Reaction of 2-Methyl-4-(alkynyloxy)cyclohexa-2,5-dienones: Catalyst-Free Access to Hydrobenzofuran Derivatives
|
1.00 |
|
Dynamic Kinetic Resolution Enabled Synthesis of Planar and Central Chiral Ferrocenes
|
1.00 |
|
Electroreductive Cross-Coupling of Cyclopropyl Ketones and Aryl Methyl Ketones to Access 1,2,4-Triarylbenzenes via Acid-Promoted Aromatization
|
1.00 |
|
14-, 30-, and 56-Membered Azamacrocyclic Mannich Bases Built on Bispyrrolylphenylene Platforms: Isolation and Initial Anion Binding
|
1.00 |
|
Two-Step Strategy to Design Organo-Fluorophore: Engaging Palladium Catalysis for Carbo-Oxygenative Cyclization of Chloroprene Derivatives
|
1.00 |
|
Photoexcited Nitroarenes: A Workhorse for Strategic Synthesis of N-Heterocycles via Reductive C–N Coupling/Cyclization Cascade
|
1.00 |
|
SuFEx-Functionalized Pyrroles via Regioselective 1,3-Dipolar Cycloaddition of Münchnones
|
1.00 |
|
Exploiting Hexafluoroisopropanol-Mediated Stereospecific Thiourea-Catalyzed C-Glycosylation of Indoles Enables Access to 2-Deoxy β-C-Indolyl Glycosides
|
1.00 |
|
Organophotoredox-Catalyzed Vinyl Group Transfer Reaction: An Introduction to 4-Vinyl-1,4-dihydropyridines
|
1.00 |
|
Blue Vitriol Catalyzed Decarboxylative C–C Cross-Coupling of α,β-Unsaturated Acids for C–H Functionalization of Unactivated Ethers
|
1.00 |
|
Access to α-Alkynyl-α-fluoroacetamides via Deacylative Alkynylation of α-Fluoro-β-ketoamides with Alkynyliodonium Salts
|
1.00 |
|
Methyl Formate Meets Water: Phosphine-Free Mn(I) Catalysis for Chemoselective Olefin amp; Carbonyl Hydrogenation
|
1.00 |
|
Ru(II)-Catalyzed Annulative Linear Dienylation with Allenyl Carbinol Acetates
|
1.00 |
|
Bifunctional 2-Aminopyridine-Catalyzed Aza-Friedel–Crafts/Oxa-6π Cascade: Synthesis of 2,2-Disubstituted Chromenes
|
1.00 |
|
3-Substituted Lawsones from Indanone Chalcones: Application of the House–Meinwald Rearrangement (HMR) for Chemoselective Ring Expansion
|
1.00 |
|
Visible-Light-Enabled Sulfonyl Radical-Triggered Cyclization Strategy for the Efficient Synthesis of Benzosultams
|
1.00 |
|
Palladium-Catalyzed Annulation of Acyl Saccharins with Norbornene via CO Shuttling
|
1.00 |
|
Metal-Free Photoredox-Catalyzed Anti-Markovnikov Phosphinothiolation of Styrenes: Chemodivergent Access to S-Alkyl-phosphinothioates and β-Keto-phosphinothioates
|
1.00 |
|
Visible-Light-Induced Bi2O3 Catalysis toward 2-fold gem-Difluoroalkylation of Quinoxalinones
|
1.00 |
|
Exploring γ-Nitroketones as 1,4-Dicarbonyl Precursors for Annulation to Pyridazines through Interrupted Nef Reaction
|
1.00 |
|
Sustainable Synthesis of N-Substituted Pyrroles via Fe-Catalyzed One-Pot Multicomponent Reaction
|
1.00 |
|
Ru(II)-Catalyzed peri-C–H Activation with Strained Alkylidene β-Lactones and β-Lactams: Selective Access to Seven- and Four-Membered Heterocycles
|
1.00 |
|
Cinchona-Functionalized Crown-Ether-Pinioned Calix[4]arene for a Scalable Asymmetric Organocatalytic Aza-Michael Addition Reaction
|
1.00 |
|
Photoinduced TBADT-Catalyzed Alkylation of Alkyl (E)-3-(2-Methacrylamidoaryl)acrylates to Access 3,4-Dihydroquinolin-2-(1H)-ones
|
1.00 |
|
Diastereoselective Synthesis of Double Axially Chiral Indole Derivatives via Friedel–Crafts Biarylation
|
1.00 |
|
Rhodium-Catalyzed [3+3] Annulation of N-Sulfonyl-1,2,3-triazole with a Homoallylic Alcohol for the Synthesis of 1,2-Dihydropyridine
|
1.00 |
|
Chirality in Abundance: A Reagent-Controlled Access to Multiple Stereoisomers of Functionalized Bishomocubanes
|
1.00 |
|
Rauhut–Currier Reaction-Inspired Intramolecular Cyclization Approach Using DBU to Access Biaryl-Fused Cycloheptatriene Derivatives
|
1.00 |
|
Desymmetrization and Atroposelective Cobalt Catalyzed C–H Annulation of Phosphinic Amides with Ynamides
|
0.83 |
|
Synthesis of Sterically Congested Z-Selective Secondary β-Enaminal
|
1.00 |
|
Palladium-Catalyzed Intramolecular meta-C–H Arylation Assisted by Nitrile Templates Under Microwave-Accelerated Conditions Accessing Fluorene Frameworks
|
1.00 |
|
Photocatalytic SN2′-Type Mono-, Di-, and Trifluoromethylation of gem-Dichlorocyclobutenones
|
1.00 |
|
Direct β-C(sp3)–H Functionalization to Carbonyls: A Route to Aldehydic Acid Derivatives
|
1.00 |
|
HFIP-Promoted Strain-Release-Driven Functionalization of Azabicyclo[1.1.0]butanes with Heterocyclobutane Trichloroacetimidates
|
1.00 |
|
Copper-Catalyzed Synthesis of Medium-Sized Cyclic Aminals via Annulation of Ketenimines and N-Acyliminium Ions
|
1.00 |
|
Vinylsilanes as Ethylene Surrogates: Rh(I)-Catalyzed Direct Hydroarylation of In Situ Generated Ethylene
|
1.00 |
|
Dearomative Indole Annulation with 2-Aminoaryldisulfide – an Approach for Accessing Polycyclic Indoline-Fused-Benzothiazine
|
1.00 |
|
One-Pot Access to Dibenzodiazepines and 9-Arylacridines from a Cyclic Dienamine
|
1.00 |
|
Copper-Catalyzed Intramolecular Carbocyclization/1,2-Migration Reaction of Allenols To Access Substituted 2-Sulfonyl Carbazoles
|
1.00 |
|
Synthesis of Tetralin and Chromane Motifs via Pd-Catalyzed Dual C(sp3)–H/C(sp2)–H Bond Activation
|
1.00 |
|
Electrochemical Direct C–H Fluorination of Hydrazones
|
1.00 |
|
N-Annulated [5]Helicenes: Syntheses, (Anti)Aromaticity and Properties
|
1.00 |
|
[4 + 2] Annulation of CF3-π-Allyl–Pd Species with Isatic Acids for Direct Access to 3-Trifluoroethyl-4-carboxylate Quinolines
|
1.00 |
|
Ligand- and Temperature-Controlled Stereodivergent Nickel-Catalyzed Hydrophenoxylation of Ynamides
|
1.00 |
|
Organocatalytic Visible-Light-Driven Metallomimetic Charge Transfer Process: Application in C(sp3)–N Bond Formation
|
1.00 |
|
Cu-Catalyzed One-Pot Synthesis of Trifluoromethylated β-Lactams by Reaction of Nitrosoarenes, Trifluorodiazoethane and Arylacetylenes
|
1.00 |
|
H-Bond- and Strain-Release-Guided Photoreaction of Alkenes, p-Quinone Methides, and Ammonium Thiocyanate
|
1.00 |
|
Strain-Release Asymmetric Multicomponent Reaction to Access Diverse N-α-Bisaryl-C3-quaternary Azetidines
|
1.00 |
|
Synthesis of Unsymmetrical 4,4′-Bipyridines through Base-Mediated Cross-Coupling between 4-Pyridyl Phosphonium Salts
|
1.00 |
|
Solution-Phase and Mechanochemical Brønsted-Acid-Catalyzed N-Alkylation of NH-Heterocycles via Hydroamination of Vinyl Ethers
|
1.00 |
|
Hydro/Fluoro-phosphoro(di)thiolation of Allenamides: Toward SN2-Selective Transition-Metal-Free Formal Hydrocarbonation
|
0.67 |
|
Enantioselective [4 + 2] Annulation Reaction of C1-Ammonium Enolate and Azadiene for 3,4-Dihydroquinolinones Synthesis
|
1.00 |
|
Total Synthesis of Lucidimines/Ganocalicines A/B, Sinensine E, and Ganocochlearine E
|
1.00 |
|
Temperature Dependent Divergent Radical Oxidative Amidation Engaging Arylglyoxyl Radicals
|
1.00 |
|
Direct Ether Synthesis Utilizing the Carbonyl Umpolung Reaction
|
0.13 |
|
Total Synthesis of Chondrochloren A
|
1.00 |
|
Copper(I)-Catalyzed Amide Oxazoline-Directed, Atom-Economic C–H Selenylation of (Hetero)Arenes under External Oxidant-Free Conditions
|
1.00 |
|
Collective Total Synthesis of (+)- and (−)-Baoslingzhines F–H, (+)- and (−)-Chizhiene C, and (+)- and (−)-Lingzhines E and F
|
1.00 |
|
Engaging Photoexcited ortho-Substituted Nitroarenes and Aryl/Alkyl Boronic Acids in Reductive C–N Coupling
|
1.00 |
|
Unified Photoredox Strategy for Selective Access to Hydroisoquinoline and Benzosultam via Tether Modulation of Allylamine
|
0.67 |
|
Photoredox-Enabled and Thianthrenation-Promoted Access to Arene Sulfinamides En Route to Other S(VI) Compounds
|
1.00 |
|
Construction of the Dictamnine Framework via an Alkynylation/Cyclization Cascade Enabled by Quinolinone-Fused Cyclic Diaryliodonium Salts
|
0.13 |
|
Access to Alkylative/Hydrodefluorination of Trifluoromethyl Ketones Using Photoexcited Dihydropyridines
|
1.00 |
|
Conia-Ene Cyclization of Pyrazolones with o-Alkynyl Aldehydes: A Strategic Shift from Classical Condensation to Spiroannulation
|
1.00 |
|
Synthesis of Uracil Containing Oxazolidinone Derivatives by Using Uracil-BX and NaHCO3 as a Solid Surrogate of CO2
|
1.00 |
|
Nickel-Catalyzed Alkenylation of N-Heteroarenes with Fluorinated Alcohols: Direct Access to CF3-Embedded Olefins
|
1.00 |
|
Access to Biaryls via Anilide C–N Bond Activation through Photocatalytic Radical Truce–Smiles Rearrangement
|
1.00 |
|
Harnessing the Umpolung Reactivity of 3-Pyrrol-1-yloxindoles: Iodine-Catalyzed Cross-Dehydrogenative Coupling for the Direct Synthesis of 3,3-Disubstituted Oxindoles
|
1.00 |
|
UV Light-Mediated Generation of Ketyl Radicals with a Concurrent 1,2-Boron Shift and One-Pot Synthesis of Benzoxaboroles under Continuous-Flow Conditions
|
1.00 |
|
Dihydrogen Phosphate Anion-Templated Supramolecular Assembly with Bistable [3]Rotaxane: Application in Selective and Sensitive Picric Acid Detection
|
1.00 |
|
Cyclocarbonickelation–Arylation Cascade under Ligand-Free Conditions: Access to Dibenzoxepine, Oxathiepine, and Thiazepine Frameworks and Mechanistic Insights
|
0.60 |
|
Visible-Light-Induced [5 + 1] Annulation of Vinyl Cyclopropane with Nitrene
|
1.00 |
|
Silicon-Assisted Ferrier Rearrangement in Preparation of C3-Silyl Glycosides
|
1.00 |
|
A Modular Approach to Access 1,4-Benzoxazinones, Spirooxazolidinones, and 4,1-Benzoxazepinones via Oxidative Aryl C–N Bond Formation Using Catalytic Hypervalent Iodine
|
1.00 |
|
Dual N-Heterocyclic Carbene/Thiourea Catalysis Enabled Asymmetric Dearomative Michael Addition of C3-Fluorooxindoles to 2-Nitrobenzofurans
|
1.00 |
|
Merging Aldehydic C–H Activation with Strain Release C–C Bond Cleavage of Bicyclo[1.1.0]butanes under Rh(III) Catalysis
|
1.00 |
|
Co(III)-Catalyzed Three-Component Cascade for the Synthesis of α-Quaternary Acyclic Nitriles via C–H Bond Activation
|
1.00 |
|
Photochemical, Catalyst-Free [2+2] Cycloaddition of Coumarin-3-carboxylates with Alkenes
|
1.00 |
|
Copper-Catalyzed Diazo Controlled Annulation of Naphthylamines to Benzo[g]indoles
|
1.00 |
|
Copper–Iron-Catalyzed Cross-Coupling of ortho-Substituted Sulfonamides with Sterically Hindered (Hetero)aryl Chlorides and Alkyl Halides: Synthesis of Sulfonamide Drugs
|
1.00 |
|
Steric Effects of β-Annulated Pyrroles Trigger the Formation of Ethynylene-Bridged Hexaphyrinogen versus Ethynylene-Cumulene-Linked Aromatic [30] π Hexaphyrin
|
0.60 |
|
Mechanochemical Bis-Spirocyclopropanation Reaction and Ring Rearrangement to 1-Oxaspiro[4.5]decadienones
|
1.00 |
|
Pristine Facet of Alkynyl-Prins Vinyl Carbocations for the Functionalization of Inactivated C(sp3)–H Bonds: A Highly Selective [1,5]-Hydride Migration vs. Concerted C–H Insertion
|
1.00 |
|
Palladium(II)-Catalyzed [3 + 2] Annulation of Aromatic Triflamides via Maleimide-Relayed Dual C–H Activation Process
|
1.00 |
|
Microwave-Assisted Precise Synthesis of Alkyl/Aryl-Modified Triazolyl-Phenylalanine Hybrids and Peptide Modifications through Multicomponent Reaction
|
1.00 |
|
Stereoselective Synthesis of Diaza-Hexatrienes via [1,6]-O-to-N Group Transfer Strategy
|
1.00 |
|
Photochemical Carbene-Transfer Reaction of Vinyldiazo Compounds: Synthesis of 1-Pyrrolines via Methylenation/[2+3] Annulation
|
1.00 |
|
Noncovalent N-Heterocyclic Carbene Catalysis Enables Asymmetric Conjugate Addition of 2-Benzofuranones to Terminal C-Electrophiles
|
1.00 |
|
Four-Step Synthesis of (±)-Nanolobatolide via Site-Selective Functionalization
|
1.00 |
|
Reductant-Controlled Access to Sulfinamides from Aliphatic Primary Amines
|
1.00 |
|
Photo-Triggered Hydrophosphination of Azoarenes: An Additive-Free Methodology
|
1.00 |
|
A De Novo Approach for the Atroposelective Synthesis of C5 Aryl Pyrazoles via 5-endo-dig Cyclization
|
1.00 |
|
Syntheses of Millingtonine and Incargranine A Following a Unified Cross-Dimerization-Aromatization Strategy
|
1.00 |
|
Ruthenium(II)-Catalyzed Macrocyclization via Site-Selective Hydroarylation of Alkynes: Access to Indoline-Braced Metacyclophanes
|
1.00 |
|
Development of Cationic Enantioselective Domino Carbopalladation/C(sp3)–Pd Capture Using N-Tosylhydrazones as Diazo Precursors§
|
1.00 |
|
Stereoselective and Regioselective Synthesis of Chiral Dihydrofurocoumarins as Glycohybrids
|
1.00 |
|
Cobalt-Catalyzed Regio- and Enantioselective Reductive Coupling of 1,3-Enynes with Imines
|
1.00 |
|
Nonalternant Acenaphthylene-Fused Carbaporphyrins: Topological Modulation of π-Delocalization, (Anti)aromaticity, and BIII Coordination
|
0.80 |
|
Copper-Catalyzed Regioselective Hydroamination and Dual Annulation of 2-Alkynyl Indole-3-carbonitriles: An Assembly of Functionalized Amino-Benzo[h]indolo[3,2-c][1,6]naphthyridines
|
1.00 |
|
Organocatalytic Asymmetric Friedel–Crafts Reaction of Prochiral 3,4-Fused Pyrroles via a Desymmetrization/Kinetic Resolution Sequence
|
1.00 |
|
Enantioselective Synthesis of the Proposed Structure of (−)-Taiwaniadduct F
|
1.00 |
|
Skeletal Editing Via CH→N Atom Swapping in Fused Imidazoles: Access to Triazolo[5,1-a]isoquinoline, Triazolo[1,5-a]quinoline, and Triazolo-[1,5-a]pyridines Frameworks
|
1.00 |
|
Electrophotocatalytic Radical Cascade Reaction for the Synthesis of Trifluoromethylated Spirocyclobutyl Oxindoles
|
1.00 |
|
Nitrene Transfer Radical Relay: A Light-Enabled Strategy for Accessing Tetrahydropyridine
|
0.25 |
|
Copper-Catalyzed Domino Bis-[3 + 2]-Annulation of Ethynyl Cyclic Carbonates with Trifluoromethyl Azlactones
|
1.00 |
|
Remote meta-C–H Functionalization of Baylis–Hillman Adducts
|
1.00 |
|
N-Selective Difluoromethylation of 4-Hydroxyquinolines
|
0.25 |
|
Cross-Electrophile Sulfonylation Involving Morita–Baylis–Hillman Acetates and Alkyl Halides: Access to Allyl–Alkyl Sulfones
|
1.00 |
|
Divergent Synthesis of Eudesmane Sesquiterpenoids
|
1.00 |
|
One-Pot Synthesis of Sulfilimines from Sulfenamides Using Aldehydes as an Alkyl Source
|
1.00 |
|
Sulfinyl-Imine-Assisted Asymmetric [3,3]-Sigmatropic Rearrangement: Generation of Tertiary and Quaternary Stereocenters
|
1.00 |
|
Three-Component Reaction through Rh(III)-Catalyzed Strain Release of Bicyclo[1.1.0]butanes
|
1.00 |
|
Stereoselective Electrosynthesis of Imidazolines through Coupling and Ring Restructuring of Alkoxyoxazoles with α-Amino Carbonyls
|
1.00 |
|
Tropone-Enabled Pd-Catalyzed C(sp2)–H Functionalization of Phenylalanine: Switchable Access to Indoline and Olefinate
|
1.00 |
|
Palladium-Catalyzed Synthesis of Quinolinyl Lactones via Double C(sp3)–H Functionalization
|
1.00 |
|
Pd/C-Catalyzed Hydrocarboxylation and Carbonylative Esterification of Indoles to Indole-3-carboxylic Acids and Esters
|
1.00 |
|
Electrochemical Formal (3 + 2) Cycloaddition/Imidation Cascade: Easy Access to Triazabicyclo-[3.3.0] Scaffolds
|
1.00 |
|
Photoexcited Palladium-Catalyzed C–N Bond Formation: A Unified Approach for N-Arylation of NH-Sulfoximines
|
1.00 |
|
One-Pot Construction of Polycyclic Indoles through Temperature-Dependent 1,3-Dipolar Cycloaddition and Cascade Rearrangement
|
1.00 |
|
Lewis Acid-Assisted Formal C═S Insertion of Thioindolinones to Bicyclobutanes: Diastereoselective Access to Trisubstituted Cyclobutanethiols
|
1.00 |
|
Easy Access to Vinylene-Linked Conjugated Homopolymers from Phosphonates via an O2-Mediated Aldehyde-Free Strategy
|
1.00 |
|
Development of a Cationic Cascade Trailing into Piancatelli Rearrangement En Route to Skeletally Diverse Polycyclic Frameworks
|
1.00 |
|
One-Step Radical α–α Coupling Accesses Helical Near-Infrared 3-Pyrrolyl Boron Dipyrromethene Dimers
|
0.63 |
|
Ligand-Controlled Stereodivergent Hydroalkynylation of Purine Allenamines to Access Functionalized trans- and cis-1,3-Enynes
|
1.00 |
|
Diverse Ring Opening and Annulation Catalyses of Isoxazole To Construct Valuable Functionalized Pyrroles, Pyridines, and Nicotinamides
|
1.00 |
|
HFIP-Mediated Ring Opening of Bicyclo[1.1.0]butanes with Hydroperoxides for Diastereoselective Access to Peroxycyclobutanes
|
1.00 |
|
Total Synthesis of Passifetilactone D, Cryptorigidifoliol I, and Cryptorigidifoliol B Isomers Enabled by Ghosez Lactonization
|
1.00 |
|
Manganese-Catalyzed Synthesis of γ-Hydroxy Phosphine Oxides by Addition of Phosphine Oxides to Allylic Alcohols
|
1.00 |
|
Access to Branched 1,3-Dienes via Innate C(sp3)–H Functionalization of 8-Methylquinolines
|
1.00 |
|
Copper-Catalyzed Selective 1,2-Reduction of Quinolines
|
1.00 |
|
Regioselective Divergent Benzannulations of Vinyl Sulfoxonium Ylides with Electron-Deficient Alkynes
|
1.00 |
|
Arylthianthrenium Salts Enabled Palladium-Catalyzed Regioselective Arylation: Access to Value-Added 7-Azaindoles
|
1.00 |
|
Strain-Release Functionalization of iN/i-Aryl Bicyclo[1.1.0]butane Sulfonamides to Access Spirocyclic Sultams
|
1.00 |
|
Diastereoselective Synthesis of iN/i-Glycosides via Buchwald–Hartwig Coupling
|
1.00 |
|
A Visible-Light Organophotoredox-Catalyzed ianti/i-Markovnikov Hydrocarbamoylation of Unactivated Alkene and Cyclization Cascade via Radical Relay
|
1.00 |
|
Stereoselective Fluoro-Deuteration/Chalcogenation/Halogenation of gem-Difluoroallenes (DFAs)
|
1.00 |
|
Construction of Acyclic Vicinal All-Carbon Quaternary and Tertiary Carbon Stereocenters via a Stereoselective Claisen Rearrangement
|
1.00 |
|
Alectinib Synthesis through Formal α-Arylation of Enone
|
1.00 |
|
A Quadruple Relay Approach Toward Highly Functionalized Furans: Merging Carbene Insertion, Semi-Pinacol Rearrangement, Decarbonylation, and Paal–Knorr Cyclization
|
1.00 |
|
Catalytic Atroposelective Coumarin Alkenylation
|
1.00 |
|
Ligand-Enabled Room-Temperature Three-Component Strategy for Mono-α-arylation of Acetone with Cyclic Diaryliodonium Salts and Alkenes
|
1.00 |
|
Photocatalytic Smiles Rearrangement at Remote C(spsup3/sup)–H Bonds
|
1.00 |
|
A Thermal [2+2] Cycloaddition/Retro-4π-Electrocyclization Reaction of ip/i-Quinone Methides with Alkyne and a Mechanistic Investigation: Ingress of a Vinyl Fuchsone Pharmacophore
|
0.67 |
|
DAST Enabled Synthesis of Fluorinated Amides and Fatty Acid Amides Including Drugs under Ambient Conditions
|
0.50 |
|
Inherent Weakly Coordinating Oxo-Group-Directed Ruthenium(II)-Catalyzed C5 Functionalization of 2-Arylquinolin-4(1H)-ones
|
1.00 |
|
Photoinduced Ligated Boryl Radical-Mediated Alkynylation of Inert Iodoalkanes
|
1.00 |
|
Asymmetric Total Synthesis of (+)-Shearilicine
|
1.00 |
|
C–F Bond Functionalization: Controlled Didefluorination of o-Trifluoromethyl Benzylamines
|
1.00 |
|
Convergent Synthesis of Functionalized Indolines from Alkyl Aryl Tertiary Amines and Diazoesters via Visible Light-Driven [4 + 1]-Annulation Approach
|
1.00 |
|
Chiral Transient Directing Group Enabled Palladium-Catalyzed Atroposelective C–H Vinylation of Biaryl Aldehydes with Vinyl Silane
|
1.00 |
|
Copper-Catalyzed Enantioselective Acylcyanation of Alkenes
|
1.00 |
|
Diastereoselective Synthesis of Cyclic and Spirocyclic Quaternary Carbons via Iron-Catalyzed Ring Contraction of Cyclic Ketones: A Formal Synthesis of Perhydrohistrionicotoxin
|
1.00 |
|
Iridium-Catalyzed Enantioselective Allenylic Cyanomethylation
|
1.00 |
|
NBS-Enabled Rapid Cyclization of 5,6-Diaryl Dipyrroethenes to Access imeso/i-Tetraaryl Porphycenes
|
1.00 |
|
Silicon-Assisted Photocatalyzed C–O Bond Cleavage: Broader Applications and Mechanistic Investigations
|
1.00 |
|
Unified Photoredox-Catalyzed Aerobic Oxidative Dynamic Kinetic Asymmetric Transformation for C–N Atropoisomers Mediated by Chiral Organophosphites
|
1.00 |
|
Unveiling Palladium Catalysis to Access Oxepino-indole through Sequential Oxycyclization Utilizing η3-π-Allyl Reactivity
|
1.00 |
|
Ruthenium(II)-Catalyzed Annulation of Vinyl Sulfoxonium Ylides with Arynes for the Rapid Synthesis of Functionalized 1-Naphthols
|
1.00 |
|
HFIP-Mediated Spiro-annulation of Bicyclo[1.1.0]butanes with α-Halo Hydroxamates: Access to Functionalized Spirocyclobutenes
|
0.71 |
|
Uracil-BX: Bench-Stable Cyclic Hypervalent Iodine Reagents for Umpolung Functionalization
|
1.00 |
|
Photosensitized Energy-Transfer-Mediated Aminoformylation of Alkenes
|
1.00 |
|
Four-Component Selenoazaindolylation-Alkoxylation of Styrenes for the Synthesis of Azaindolyl β-Alkoxyalkyl Selenoethers
|
1.00 |
|
Visible-Light-Induced Flavin Catalysis: A Green Route to Naphtho[2,1-b]furans via an o-(Naphtho)quinone Intermediate
|
1.00 |
|
Ir(III)-Photocatalyzed Stereoselective Synthesis of 2-Azadienes
|
1.00 |
|
Total Syntheses of Avapyran and Dysiquinol D through a Stereoconvergent Fusion of Dihydrobenzopyran
|
1.00 |
|
NBS-Promoted Synthesis of Maleimides by Oxidative Dearomatization of Pyrroles: Mechanistic Investigations Using Online MS in Real-Time
|
0.75 |
|
All-Aza meso-Benzo-Fused Triphyrins(2.1.1): Large Bathochromic Shift and Intensified Absorption via π-Extended Conjugation
|
1.00 |
|
(Methyl)thianthrenium Salt Enabled Monoselective N-Methylation and N-(13C-Methyl) Labeling: Late-Stage Functionalization of Arylamides
|
1.00 |
|
Regioselective Spirocyclopropyl C–C Cleavage and Ketene–Imine-Triggered Skeletal Rearrangement for the Synthesis of α-Carboline
|
1.00 |
|
Direct Assembly of Functionalized 3-Hydroxypyridine N-Oxides via Cascade Nitration/Hydroxylative aza-Annulation Reactions
|
1.00 |
|
Diastereodivergent Synthesis of Vinylsilanes Using Solid Silylzinc Reagent
|
1.00 |
|
α-Amination at BODIPY and BOPHY Core via Metal-Free Regiospecific Cross Dehydrogenative Coupling Reaction Toward the Development of Lysotracker
|
1.00 |
|
One-Pot Regioselective Functionalization of Quinone Imine Ketals: Direct Access to iortho/i-Substituted Anilines from Arylamines
|
1.00 |
|
An Oxidative Palladium-Catalyzed Remote imeta/i-Selective Homo-Biaryl Coupling Assisted by Nitrile Directing Templates
|
1.00 |
|
Intramolecular Radical Oxidative Cyclization: Access to Fused-Bicyclo[3.1.0] Hexanes from igem/i-Dihalo Olefins
|
1.00 |
|
Efficient Synthesis of Pseudoindoxyls from 2-Nitrobenzylidenemalonates and Indoles
|
1.00 |
|
Catalytic Asymmetric Total Synthesis of Naturally Occurring iAmaryllidaceae/i Alkaloid, (+)-11-Hydroxyvittatine
|
1.00 |
|
Cobalt-Catalyzed Regio-, Diastereo-, and Enantioselective Reductive Coupling of Internal Alkynes with Cyclobutenes
|
1.00 |
|
Sterically Hindered and Electron-Deficient 2,4,6-Tri-itert/i-butylpyrimidinium as a π-Lewis Acid Toward Organocatalytic Silyl Protection of Carbohydrates Using Trialkyl/aryl Silanes
|
1.00 |
|
Peptide Functionalization with Dithioate and Trithioate Groups: A CSsub2/sub-Mediated Solid-Phase Approach
|
1.00 |
|
Manganese Complex-Catalyzed (De)hydrogenative Cyclization toward the Selective Synthesis of 2-Substituted and 2,3-Disubstituted 4-Quinolones
|
1.00 |
|
Scalable Photoinduced Cycloaddition for the Synthesis of Biorelevant Oxazoles
|
0.50 |
|
Total Synthesis of (±)-Streptoglyceride A and of Putative (±)-Streptoglyceride C
|
1.00 |
|
Triplet Excited Nitroarene Converts Aryl Alkynes to Ketones by Deleting a Carbon Atom
|
1.00 |
|
Leveraging Borylcupration for Enantioselective Cascade Spiroannulation: Access to Spirophthalide Boronates
|
1.00 |
|
NHC-Catalyzed Allylation of Aldehydes with MBH Carbonates and Their Michael Addition–Elimination-Cope Rearrangement Cascade: A Route to rac-Sacubitril
|
1.00 |
