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Outgoing claims: the papers this work cites, builds on, or argues with.
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Total synthesis of FK506 and an FKBP probe reagent, [C(8),C(9)-13C2]-FK506
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Total Synthesis of (−)-Reserpine Using the Chiron Approach
inferredcites →https://doi.org/10.1021/op970115wopenalex-snapshot
A Calorimetric Investigation To Safely Scale-Up a Curtius Rearrangement of Acryloyl Azide
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.12.131openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.02.082openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.05.101openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.11.012openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.10.079openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.11.124openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.08.065openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.08.083openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.09.034openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154226openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.yrtph.2007.06.008openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.0c02700openalex-snapshot
Palladium-Catalyzed C–C Bond Activation of Cyclopropenone: Modular Access to Trisubstituted α,β-Unsaturated Esters and Amides
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02846openalex-snapshot
Selectivity Effects of Hydrogen Acceptors and Catalyst Structures in Alcohol Oxidations Using (Cyclopentadienone)iron Tricarbonyl Compounds
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01240openalex-snapshot
Toward a Unified Mechanism for Oxoammonium Salt-Mediated Oxidation Reactions: A Theoretical and Experimental Study Using a Hydride Transfer Model
inferred← citeshttps://doi.org/10.1021/acs.oprd.2c00005openalex-snapshot
Large-Scale Amidations in Process Chemistry: Practical Considerations for Reagent Selection and Reaction Execution
inferred← citeshttps://doi.org/10.1021/acs.oprd.4c00177openalex-snapshot
Pinnick Oxidation on Scale: Process Development of a BDK Inhibitor
inferred← citeshttps://doi.org/10.1021/acs.oprd.5b00101openalex-snapshot
Investigating Scale-Up and Further Applications of DABAL-Me 3 Promoted Amide Synthesis
inferred← citeshttps://doi.org/10.1021/acs.oprd.6c00001openalex-snapshot
Decoding Reactions in Process Chemistry: A Quarter-Century Analysis of Trends and Transformations in OPR&D
inferred← citeshttps://doi.org/10.1021/acs.oprd.8b00199openalex-snapshot
Using Data Analysis To Evaluate and Compare Chemical Syntheses
inferred← citeshttps://doi.org/10.1021/acs.oprd.8b00237openalex-snapshot
Evaluating the Impact of a Decade of Funding from the Green Chemistry Institute Pharmaceutical Roundtable
inferred← citeshttps://doi.org/10.1021/acs.oprd.8b00456openalex-snapshot
Safe and Scalable Aerobic Oxidation by 2-Azaadamantan-2-ol (AZADOL)/NOx Catalysis: Large-Scale Preparation of Shi’s Catalyst
inferred← citeshttps://doi.org/10.1021/acs.oprd.9b00376openalex-snapshot
Mutagenic Impurities in 1-Hydroxybenzotriazole (HOBt)
inferred← citeshttps://doi.org/10.1021/acs.organomet.5b00988openalex-snapshot
Palladium-Catalyzed Regioselective Arylation of Pyrazolo[1,5-a]pyridines via C–H Activation and Synthetic Applications on P38 Kinase Inhibitors
inferred← citeshttps://doi.org/10.1021/acs.organomet.8b00617openalex-snapshot
Reductive Elimination to Form C(sp3)–N Bonds from Palladium(II) Primary Alkyl Complexes
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01543openalex-snapshot
Electroreductive Access to 1,2-Aminoalcohols via Cross Aza-Pinacol Coupling of N-Acyl Diarylketimines and Aldehydes
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02537openalex-snapshot
Titanium-Promoted Cross-Coupling for the Selective Synthesis of Polysubstituted, Conjugated Amides
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c03107openalex-snapshot
Skeletal Editing of α-Oxoketene- N , S -Acetals into Amides via Cooperative Base-Promoted/Copper-Catalyzed Amidation
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02793openalex-snapshot
Iron-Catalyzed Coupling of Methyl N -Heteroarenes with Primary Alcohols: Direct Access to E -Selective Olefins
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04305openalex-snapshot
Cobalt-Catalyzed Migrational Isomerization of Styrenes
inferred← citeshttps://doi.org/10.1021/acscatal.1c00242openalex-snapshot
Photoinduced Metal-Free α-C(sp3)–H Carbamoylation of Saturated Aza-Heterocycles via Rationally Designed Organic Photocatalyst
inferred← citeshttps://doi.org/10.1021/acscatal.5b00237openalex-snapshot
Palladium Nanoparticles Supported in the Nanospaces of Imidazolium-Based Bifunctional PMOs: The Role of Plugs in Selectivity Changeover in Aerobic Oxidation of Alcohols
inferred← citeshttps://doi.org/10.1021/acscatal.5c01646openalex-snapshot
The Evolving Landscape of Industrial Biocatalysis in Perspective from the ACS Green Chemistry Institute Pharmaceutical Roundtable
inferred← citeshttps://doi.org/10.1021/acscatal.7b01317openalex-snapshot
Acceleration of Pd-Catalyzed Amide N-Arylations Using Cocatalytic Metal Triflates: Substrate Scope and Mechanistic Study
inferred← citeshttps://doi.org/10.1021/acscatal.7b01543openalex-snapshot
Hybrid Organo- and Biocatalytic Process for the Asymmetric Transformation of Alcohols into Amines in Aqueous Medium
inferred← citeshttps://doi.org/10.1021/acscentsci.6b00187openalex-snapshot
Palladium-Catalyzed Cross Coupling of Secondary and Tertiary Alkyl Bromides with a Nitrogen Nucleophile
inferred← citeshttps://doi.org/10.1021/acsmedchemlett.5c00206openalex-snapshot
Suzuki–Miyaura Coupling of Pinacolboronic Esters Catalyzed by a Well-Defined Palladium N-Heterocyclic Carbene (NHC) Catalyst
inferred← citeshttps://doi.org/10.1021/acsomega.4c11109openalex-snapshot
Silver-Catalyzed Cascade Approach to Access Fused Pyrazolo-naphthyridine and -isoquinoline Backbones and Investigation of Their Photophysical Properties
inferred← citeshttps://doi.org/10.1021/acsomega.9b02430openalex-snapshot
Synthetic Strategy for Pyrazolo[1,5- a ]pyridine and Pyrido[1,2- b ]indazole Derivatives through AcOH and O2-Promoted Cross-dehydrogenative Coupling Reactions between 1,3-Dicarbonyl Compounds and N -Amino-2-iminopyridines
inferred← citeshttps://doi.org/10.1021/acssuschemeng.3c02455openalex-snapshot
Bayesian Optimization as a Sustainable Strategy for Early-Stage Process Development? A Case Study of Cu-Catalyzed C–N Coupling of Sterically Hindered Pyrazines
inferred← citeshttps://doi.org/10.1021/acssuschemeng.5c00914openalex-snapshot
Flow-to-Flow Technology: Amide Formation in the Absence of Traditional Coupling Reagents Using DPDTC
inferred← citeshttps://doi.org/10.1021/acssuschemeng.7b03820openalex-snapshot
Base-Free Aerobic Oxidation of Alcohols over Copper-Based Complex under Ambient Condition
inferred← citeshttps://doi.org/10.1021/acssuschemeng.9b04347openalex-snapshot
In Situ Sulfidation of Pd/C: A Straightforward Method for Chemoselective Conjugate Reduction by Continuous Hydrogenation
inferred← citeshttps://doi.org/10.1021/cr040679fopenalex-snapshot
Large-Scale Oxidations in the Pharmaceutical Industry
inferred← citeshttps://doi.org/10.1021/cr0505268openalex-snapshot
Selected Patented Cross-Coupling Reaction Technologies
inferred← citeshttps://doi.org/10.1021/cr200251dopenalex-snapshot
Synthesis of Pyridine and Dihydropyridine Derivatives by Regio- and Stereoselective Addition to N -Activated Pyridines
inferred← citeshttps://doi.org/10.1021/cs300821uopenalex-snapshot
Baeyer–Villiger Oxidation Using Hydrogen Peroxide
inferred← citeshttps://doi.org/10.1021/ie301821kopenalex-snapshot
Hydrodynamics of Liquid–Liquid Dispersion in an Advanced-Flow Reactor
inferred← citeshttps://doi.org/10.1021/ja0764052openalex-snapshot
Nucleophilic Carbene and HOAt Relay Catalysis in an Amide Bond Coupling: An Orthogonal Peptide Bond Forming Reaction
inferred← citeshttps://doi.org/10.1021/ja105194sopenalex-snapshot
Controlled and Chemoselective Reduction of Secondary Amides
inferred← citeshttps://doi.org/10.1021/ja110940copenalex-snapshot
Highly Efficient, Organocatalytic Aerobic Alcohol Oxidation
inferred← citeshttps://doi.org/10.1021/ja301769ropenalex-snapshot
Replacing Conventional Carbon Nucleophiles with Electrophiles: Nickel-Catalyzed Reductive Alkylation of Aryl Bromides and Chlorides
inferred← citeshttps://doi.org/10.1021/ja303181mopenalex-snapshot
Scope of the Palladium-Catalyzed Aryl Borylation Utilizing Bis-Boronic Acid
inferred← citeshttps://doi.org/10.1021/ja3047816openalex-snapshot
Palladium-Catalyzed C(sp3)–H Arylation of Diarylmethanes at Room Temperature: Synthesis of Triarylmethanes via Deprotonative-Cross-Coupling Processes
inferred← citeshttps://doi.org/10.1021/ja400345copenalex-snapshot
Azaaldol Condensation of a Lithium Enolate Solvated by N,N,N′,N′-Tetramethylethylenediamine: Dimer-Based 1,2-Addition to Imines
inferred← citeshttps://doi.org/10.1021/ja4009776openalex-snapshot
Palladium-Catalyzed Direct Arylation of Methyl Sulfoxides with Aryl Halides
inferred← citeshttps://doi.org/10.1021/ja403076uopenalex-snapshot
Enediolate–Dilithium Amide Mixed Aggregates in the Enantioselective Alkylation of Arylacetic Acids: Structural Studies and a Stereochemical Model
inferred← citeshttps://doi.org/10.1021/ja4126609openalex-snapshot
Photoinduced, Copper-Catalyzed Alkylation of Amides with Unactivated Secondary Alkyl Halides at Room Temperature
inferred← citeshttps://doi.org/10.1021/ja504365zopenalex-snapshot
Method of Continuous Variation: Characterization of Alkali Metal Enolates Using 1H and 19F NMR Spectroscopies
inferred← citeshttps://doi.org/10.1021/ja512903gopenalex-snapshot
Rational Ligand Design for the Arylation of Hindered Primary Amines Guided by Reaction Progress Kinetic Analysis
inferred← citeshttps://doi.org/10.1021/ja7100642openalex-snapshot
Lithium Enolates of Simple Ketones: Structure Determination Using the Method of Continuous Variation
inferred← citeshttps://doi.org/10.1021/ja800250qopenalex-snapshot
Lithium Hexamethyldisilazide-Mediated Enolizations: Influence of Triethylamine on E/Z Selectivities and Enolate Reactivities
inferred← citeshttps://doi.org/10.1021/ja807110nopenalex-snapshot
2-Iodoxybenzenesulfonic Acid as an Extremely Active Catalyst for the Selective Oxidation of Alcohols to Aldehydes, Ketones, Carboxylic Acids, and Enones with Oxone
inferred← citeshttps://doi.org/10.1021/ja8091449openalex-snapshot
Cross-Coupling Reactions of Aromatic and Heteroaromatic Silanolates with Aromatic and Heteroaromatic Halides
inferred← citeshttps://doi.org/10.1021/ja902558jopenalex-snapshot
Hydrazides as Tunable Reagents for Alkene Hydroamination and Aminocarbonylation
inferred← citeshttps://doi.org/10.1021/ja904380qopenalex-snapshot
Isoquinoline Synthesis via Rhodium-Catalyzed Oxidative Cross-Coupling/Cyclization of Aryl Aldimines and Alkynes
inferred← citeshttps://doi.org/10.1021/ja9047784openalex-snapshot
Lithium Phenolates Solvated by Tetrahydrofuran and 1,2-Dimethoxyethane: Structure Determination Using the Method of Continuous Variation
inferred← citeshttps://doi.org/10.1021/jacs.2c06154openalex-snapshot
Catalytic Enantioselective α-Alkylation of Amides by Unactivated Alkyl Electrophiles
inferred← citeshttps://doi.org/10.1021/jacs.2c07207openalex-snapshot
Preparation of Highly Reactive Lithium Metal Dendrites for the Synthesis of Organolithium Reagents
inferred← citeshttps://doi.org/10.1021/jacs.2c09341openalex-snapshot
Lithiated Oppolzer Enolates: Solution Structures, Mechanism of Alkylation, and Origin of Stereoselectivity
inferred← citeshttps://doi.org/10.1021/jacs.4c05881openalex-snapshot
Cooperative Phosphine-Photoredox Catalysis Enables N–H Activation of Azoles for Intermolecular Olefin Hydroamination
inferred← citeshttps://doi.org/10.1021/jacs.5b08707openalex-snapshot
Evolution of C–H Bond Functionalization from Methane to Methodology
inferred← citeshttps://doi.org/10.1021/jacs.5b09524openalex-snapshot
Solid-State and Solution Structures of Glycinimine-Derived Lithium Enolates
inferred← citeshttps://doi.org/10.1021/jacs.6b04917openalex-snapshot
Total Synthesis of (+)-SCH 351448: Efficiency via Chemoselectivity and Redox-Economy Powered by Metal Catalysis
inferred← citeshttps://doi.org/10.1021/jacs.6b05481openalex-snapshot
Lithium Enolates Derived from Pyroglutaminol: Mechanism and Stereoselectivity of an Azaaldol Addition
inferred← citeshttps://doi.org/10.1021/jacs.6b11673openalex-snapshot
Lithium Enolates in the Enantioselective Construction of Tetrasubstituted Carbon Centers with Chiral Lithium Amides as Noncovalent Stereodirecting Auxiliaries
inferred← citeshttps://doi.org/10.1021/jacs.6c07181openalex-snapshot
Nickel-Catalyzed Remote Substitution of Alcohols
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