Research graph
References from Reductive C–O Bond Cleavage and Borylation of Carboxylic Esters. Local targets link to admitted publications; unresolved targets remain external evidence.
Metallaphotoredox-Enabled Deoxygenative Arylation of Alcohols
10.1038/s41586-021-03920-6 · 2021 · External reference
Hydroxyl Groups in Synthetic and Natural-Product-Derived Therapeutics: A Perspective on a Common Functional Group
10.1021/acs.jmedchem.9b00179 · 2019 · External reference
A Systematic Cheminformatics Analysis of Functional Groups Occurring in Natural Products
10.1021/acs.jnatprod.8b01022 · 2019 · External reference
Key Green Chemistry Research Areas from a Pharmaceutical Manufacturers’ Perspective Revisited
10.1039/c8gc01276h · 2018 · External reference
Zirconium-Catalysed Direct Substitution of Alcohols: Enhancing the Selectivity by Kinetic Analysis
10.1039/d1cy01219c · 2021 · External reference
Safe-and-Sustainable-by-Design Approach to Polyesters from Non-Oestrogenic Bisphenols
10.1038/s41893-025-01672-z · 2025 · External reference
Nickel-Catalyzed Alkylation of Oxindoles with Secondary Alcohols
10.1021/acs.joc.3c00402 · 2023 · External reference
Borrowing Hydrogen for Organic Synthesis
10.1021/acscentsci.1c00125 · 2021 · External reference
From Racemic Alcohols to Enantiopure Amines: Ru-Catalyzed Diastereoselective Amination
10.1021/ja5058482 · 2014 · External reference
Transition Metal-Catalyzed Allylic Substitution Reactions with Unactivated Allylic Substrates
10.1039/c5cs00144g · 2015 · External reference
Titanium: A Unique Metal for Radical Dehydroxylative Functionalization of Alcohols
10.1055/a-1406-0484 · 2021 · External reference
Recent Progress on Transition-Metal-Mediated Reductive C(Sp3)–O Bond Radical Addition and Coupling Reactions
10.1055/a-1848-3005 · 2022 · External reference
Ti-Catalyzed Dehydroxylation of Tertiary Alcohols
10.1021/acs.orglett.2c03119 · 2022 · External reference
C–OH Bond Activation for Stereoselective Radical C-Glycosylation of Native Saccharides
10.1021/jacs.4c11857 · 2024 · External reference
Direct Deoxygenative Formylation of Ketones with Titanium
10.1021/acs.orglett.5c01624 · 2025 · External reference
Unlocking C–OH Bond Activation for Radical C-Glycosylation of Native Saccharides
10.1055/a-2572-0983 · 2025 · External reference
Electroreductive Deoxygenative C–H and C–C Bond Formation from Non-Derivatized Alcohols Fueled by Anodic Borohydride Oxidation
10.1002/celc.202300420 · 2023 · External reference
Electrochemically Driven Deoxygenative Borylation of Alcohols and Carbonyl Compounds
10.1021/jacs.3c03418 · 2023 · External reference
Electrochemical Deoxygenative Silylation of Alcohols
10.1002/anie.202508697 · 2025 · External reference
Harnessing Electrochemistry for Direct Deoxygenative Silylation of Alcohols and Ketones
10.1002/anie.202509411 · 2025 · External reference
Deoxygenative Functionalization of Alcohols and Carbonyl Compounds via Electrochemical Reduction
10.1002/anie.202510069 · 2025 · External reference
Development of a Novel Electrochemical Carboxylation System Using a Microreactor
10.1039/c5ra19289g · 2015 · External reference
Synthesis of N-Boc-α-Amino Acids from Carbon Dioxide by Electrochemical Carboxylation of N-Boc-α-Aminosulfones
10.1021/acs.joc.1c01516 · 2021 · External reference
Preparation of Esters of Phosphoric Acid by the Reaction of Trivalent Phosphorus Compounds with Diethyl Azodicarboxylate in the Presence of Alcohols
10.1246/bcsj.40.935 · 1967 · External reference
Tertiary Phosphane/Tetrachloromethane, a Versatile Reagent for Chlorination, Dehydration, and P-N Linkage
10.1002/anie.197508011 · 1975 · External reference
The Catalytic Mitsunobu Reaction: A Critical Analysis of the Current State-of-the-Art
10.1039/c8ob01929k · 2018 · External reference
Redox-Neutral Organocatalytic Mitsunobu Reactions
10.1126/science.aax3353 · 2019 · External reference
Electrochemical Azo-Free Mitsunobu-Type Reaction
10.1002/anie.202402878 · 2024 · External reference
Electrochemical Synthesis of Aziridines, Pyrrolidines and Oxazolines Enabled by Azo-Free Alcohol Amination
10.1039/d5sc03101j · 2025 · External reference
Electro-Mediated PhotoRedox Catalysis for Selective C(Sp3)–O Cleavages of Phosphinated Alcohols to Carbanions
10.1002/anie.202105895 · 2021 · External reference
Photoredox-Driven Deoxygenative Cross-Coupling of Alcohols with Carbonyl Compounds
10.1021/acscatal.5c06461 · 2025 · External reference
Generation of Phosphoranyl Radicals via Photoredox Catalysis Enables Voltage-Independent Activation of Strong C-O Bonds
10.1021/acscatal.8b03592 · 2018 · External reference
Alcohols as Alkylating Agents: Photoredox-Catalyzed Conjugate Alkylation via In Situ Deoxygenation
10.1002/anie.202207150 · 2022 · External reference
Cross-Double Deoxygenative Carbon–Carbon Bond Formation between Benzyl Benzoates and Allylic Alcohols
10.1021/acscatal.4c01857 · 2024 · External reference
Nontraditional Fragment Couplings of Alcohols and Carboxylic Acids: C(Sp3)–C(Sp3) Cross-Coupling via Radical Sorting
10.1021/jacs.2c02062 · 2022 · External reference
Photoredox and NHC Enabled Deoxygenative Alcohol Homologation via Formal 1,2-Addition
10.1021/acs.orglett.3c03857 · 2024 · External reference
Photoredox Catalytic Deoxygenative Divergent Functionalizations of Alcohols Assisted by N,O-Heterocyclic Carbenes
10.1039/d4qo00115j · 2024 · External reference
Alcohols as Alkyl Synthons Enabled by Photoredox-Catalyzed Deoxygenative Activation
10.1021/acscatal.4c03560 · 2024 · External reference
Direct Construction of Quaternary Carbons from Tertiary Alcohols via Photoredox-Catalyzed Fragmentation of Tert-Alkyl N-Phthalimidoyl Oxalates
10.1021/ja408971t · 2013 · External reference
Catalyst-Free Decarboxylation of Carboxylic Acids and Deoxygenation of Alcohols by Electro-Induced Radical Formation
10.1002/chem.201905224 · 2020 · External reference
Development of an Easy-To-Handle Redox Active Group for Alcohols: Catalytic Transformation of Tertiary Alcohols to Nitriles
10.1021/acs.orglett.4c01580 · 2024 · External reference
Electrosynthetic C–O Bond Activation in Alcohols and Alcohol Derivatives
10.1002/anie.202211952 · 2023 · External reference
Tin-Free Alternatives to the Barton-McCombie Deoxygenation of Alcohols to Alkanes Involving Reductive Electron Transfer
10.2533/chimia.2016.67 · 2016 · External reference
A New Method for the Deoxygenation of Secondary Alcohols
10.1039/p19750001574 · 1975 · External reference
Progress of the Barton-McComble Methodology: From Tin Hydrides to Silanes
10.1163/156856793x00361 · 1993 · External reference
Redox-Active Thiocarbonyl Auxiliaries in Ni-Catalyzed Cross-Couplings of Aliphatic Alcohols
10.1021/acs.accounts.3c00541 · 2023 · External reference
Organic Electrosynthesis Using Toluates as Simple and Versatile Radical Precursors
10.1039/b813545b · 2008 · External reference
Toluates: Unexpectedly Versatile Reagents
10.1016/j.tet.2009.09.111 · 2009 · External reference
Chemoselective Chemical and Electrochemical Deprotections of Aromatic Esters
10.1021/ol900828x · 2009 · External reference
Electrochemical Deoxygenation of Primary Alcohols
10.1055/s-0031-1290778 · 2012 · External reference
Boryl Radical-Promoted Deoxygenative Alkylation of Benzyl Acetates
10.1055/s-0042-1751463 · 2024 · External reference
Electro-Organic Reactions. Part 1. The Cathodic Cleavage in Methanol Solution of Benzylic Carbon-Oxygen and Carbon-Fluorine Bonds
10.1039/p29730001903 · 1973 · External reference
The Electrochemical Reductive Cleavage of Carbon–Oxygen and Carbon–Fluorine Bonds in Benzyl Systems
10.1039/c29700000738 · 1970 · External reference
Practical and General Alcohol Deoxygenation Protocol
10.1002/anie.202300178 · 2023 · External reference
Stabilities and Spin Distributions of Benzannulated Benzyl Radicals
10.1021/ct700051j · 2007 · External reference
Benzylic Stabilization as a Mechanistic Tool for Studying Radical Rearrangements
10.1021/jo00109a043 · 1995 · External reference
Radical Stability—A Theoretical Perspective
10.1007/128_028 · 2006 · External reference
The Stability of Alkyl Radicals
10.1021/ja00296a007 · 1985 · External reference
Stabilization Effects in Alkanes and in Primary Secondary and Tertiary Alkyl Radicals
10.1016/s0040-4020(01)82329-2 · 1991 · External reference
Using Toluates as Simple and Versatile Radical Precursors
10.1021/ol800944p · 2008 · External reference
Some Applications of the Transition State Method to the Calculation of Reaction Velocities, Especially in Solution
10.1039/tf9353100875 · 1935 · External reference
The Synchronous-Transit Method for Determining Reaction Pathways and Locating Molecular Transition States
10.1016/0009-2614(77)80574-5 · 1977 · External reference
A Correlation of Reaction Rates
10.1021/ja01607a027 · 1955 · External reference
Electrochemical Desulfurative Borylation of Thiols, Disulfides, Thioethers and Thioacetals
10.1038/s41467-025-67363-7 · 2026 · External reference
Regioselective Electrochemical Borylation of Oxygenated Allylic Electrophiles: Method Development and Synthetic Applications
10.1021/acscentsci.5c01074 · 2025 · External reference
Tertiary Phosphane/Tetrachloromethane, a Versatile Reagent for Chlorination, Dehydration, and P-N Linkage
10.1002/anie.197508011 · ExternalCitation · doi-reference
Electro-Mediated PhotoRedox Catalysis for Selective C(Sp3)–O Cleavages of Phosphinated Alcohols to Carbanions
10.1002/anie.202105895 · ExternalCitation · doi-reference
Alcohols as Alkylating Agents: Photoredox-Catalyzed Conjugate Alkylation via In Situ Deoxygenation
10.1002/anie.202207150 · ExternalCitation · doi-reference
Electrosynthetic C–O Bond Activation in Alcohols and Alcohol Derivatives
10.1002/anie.202211952 · ExternalCitation · doi-reference
Practical and General Alcohol Deoxygenation Protocol
10.1002/anie.202300178 · ExternalCitation · doi-reference
Electrochemical Azo-Free Mitsunobu-Type Reaction
10.1002/anie.202402878 · ExternalCitation · doi-reference
Electrochemical Deoxygenative Silylation of Alcohols
10.1002/anie.202508697 · ExternalCitation · doi-reference
Harnessing Electrochemistry for Direct Deoxygenative Silylation of Alcohols and Ketones
10.1002/anie.202509411 · ExternalCitation · doi-reference
Deoxygenative Functionalization of Alcohols and Carbonyl Compounds via Electrochemical Reduction
10.1002/anie.202510069 · ExternalCitation · doi-reference
Electroreductive Deoxygenative C–H and C–C Bond Formation from Non-Derivatized Alcohols Fueled by Anodic Borohydride Oxidation
10.1002/celc.202300420 · ExternalCitation · doi-reference
Catalyst-Free Decarboxylation of Carboxylic Acids and Deoxygenation of Alcohols by Electro-Induced Radical Formation
10.1002/chem.201905224 · ExternalCitation · doi-reference
Radical Stability—A Theoretical Perspective
10.1007/128_028 · ExternalCitation · doi-reference
The Synchronous-Transit Method for Determining Reaction Pathways and Locating Molecular Transition States
10.1016/0009-2614(77)80574-5 · ExternalCitation · doi-reference
Toluates: Unexpectedly Versatile Reagents
10.1016/j.tet.2009.09.111 · ExternalCitation · doi-reference
Stabilization Effects in Alkanes and in Primary Secondary and Tertiary Alkyl Radicals
10.1016/s0040-4020(01)82329-2 · ExternalCitation · doi-reference
Redox-Active Thiocarbonyl Auxiliaries in Ni-Catalyzed Cross-Couplings of Aliphatic Alcohols
10.1021/acs.accounts.3c00541 · ExternalCitation · doi-reference
Hydroxyl Groups in Synthetic and Natural-Product-Derived Therapeutics: A Perspective on a Common Functional Group
10.1021/acs.jmedchem.9b00179 · ExternalCitation · doi-reference
A Systematic Cheminformatics Analysis of Functional Groups Occurring in Natural Products
10.1021/acs.jnatprod.8b01022 · ExternalCitation · doi-reference
Synthesis of N-Boc-α-Amino Acids from Carbon Dioxide by Electrochemical Carboxylation of N-Boc-α-Aminosulfones
10.1021/acs.joc.1c01516 · ExternalCitation · doi-reference
Nickel-Catalyzed Alkylation of Oxindoles with Secondary Alcohols
10.1021/acs.joc.3c00402 · ExternalCitation · doi-reference
Ti-Catalyzed Dehydroxylation of Tertiary Alcohols
10.1021/acs.orglett.2c03119 · ExternalCitation · doi-reference
Photoredox and NHC Enabled Deoxygenative Alcohol Homologation via Formal 1,2-Addition
10.1021/acs.orglett.3c03857 · ExternalCitation · doi-reference
Development of an Easy-To-Handle Redox Active Group for Alcohols: Catalytic Transformation of Tertiary Alcohols to Nitriles
10.1021/acs.orglett.4c01580 · ExternalCitation · doi-reference
Direct Deoxygenative Formylation of Ketones with Titanium
10.1021/acs.orglett.5c01624 · ExternalCitation · doi-reference
Cross-Double Deoxygenative Carbon–Carbon Bond Formation between Benzyl Benzoates and Allylic Alcohols
10.1021/acscatal.4c01857 · ExternalCitation · doi-reference
Alcohols as Alkyl Synthons Enabled by Photoredox-Catalyzed Deoxygenative Activation
10.1021/acscatal.4c03560 · ExternalCitation · doi-reference
Photoredox-Driven Deoxygenative Cross-Coupling of Alcohols with Carbonyl Compounds
10.1021/acscatal.5c06461 · ExternalCitation · doi-reference
Generation of Phosphoranyl Radicals via Photoredox Catalysis Enables Voltage-Independent Activation of Strong C-O Bonds
10.1021/acscatal.8b03592 · ExternalCitation · doi-reference
Borrowing Hydrogen for Organic Synthesis
10.1021/acscentsci.1c00125 · ExternalCitation · doi-reference
Regioselective Electrochemical Borylation of Oxygenated Allylic Electrophiles: Method Development and Synthetic Applications
10.1021/acscentsci.5c01074 · ExternalCitation · doi-reference
Stabilities and Spin Distributions of Benzannulated Benzyl Radicals
10.1021/ct700051j · ExternalCitation · doi-reference
The Stability of Alkyl Radicals
10.1021/ja00296a007 · ExternalCitation · doi-reference
A Correlation of Reaction Rates
10.1021/ja01607a027 · ExternalCitation · doi-reference
Direct Construction of Quaternary Carbons from Tertiary Alcohols via Photoredox-Catalyzed Fragmentation of Tert-Alkyl N-Phthalimidoyl Oxalates
10.1021/ja408971t · ExternalCitation · doi-reference
From Racemic Alcohols to Enantiopure Amines: Ru-Catalyzed Diastereoselective Amination
10.1021/ja5058482 · ExternalCitation · doi-reference
Nontraditional Fragment Couplings of Alcohols and Carboxylic Acids: C(Sp3)–C(Sp3) Cross-Coupling via Radical Sorting
10.1021/jacs.2c02062 · ExternalCitation · doi-reference
Electrochemically Driven Deoxygenative Borylation of Alcohols and Carbonyl Compounds
10.1021/jacs.3c03418 · ExternalCitation · doi-reference
C–OH Bond Activation for Stereoselective Radical C-Glycosylation of Native Saccharides
10.1021/jacs.4c11857 · ExternalCitation · doi-reference
Benzylic Stabilization as a Mechanistic Tool for Studying Radical Rearrangements
10.1021/jo00109a043 · ExternalCitation · doi-reference
Using Toluates as Simple and Versatile Radical Precursors
10.1021/ol800944p · ExternalCitation · doi-reference
Chemoselective Chemical and Electrochemical Deprotections of Aromatic Esters
10.1021/ol900828x · ExternalCitation · doi-reference
Electrochemical Desulfurative Borylation of Thiols, Disulfides, Thioethers and Thioacetals
10.1038/s41467-025-67363-7 · ExternalCitation · doi-reference
Metallaphotoredox-Enabled Deoxygenative Arylation of Alcohols
10.1038/s41586-021-03920-6 · ExternalCitation · doi-reference
Safe-and-Sustainable-by-Design Approach to Polyesters from Non-Oestrogenic Bisphenols
10.1038/s41893-025-01672-z · ExternalCitation · doi-reference
Organic Electrosynthesis Using Toluates as Simple and Versatile Radical Precursors
10.1039/b813545b · ExternalCitation · doi-reference
The Electrochemical Reductive Cleavage of Carbon–Oxygen and Carbon–Fluorine Bonds in Benzyl Systems
10.1039/c29700000738 · ExternalCitation · doi-reference
Transition Metal-Catalyzed Allylic Substitution Reactions with Unactivated Allylic Substrates
10.1039/c5cs00144g · ExternalCitation · doi-reference
Development of a Novel Electrochemical Carboxylation System Using a Microreactor
10.1039/c5ra19289g · ExternalCitation · doi-reference
Key Green Chemistry Research Areas from a Pharmaceutical Manufacturers’ Perspective Revisited
10.1039/c8gc01276h · ExternalCitation · doi-reference
The Catalytic Mitsunobu Reaction: A Critical Analysis of the Current State-of-the-Art
10.1039/c8ob01929k · ExternalCitation · doi-reference
Zirconium-Catalysed Direct Substitution of Alcohols: Enhancing the Selectivity by Kinetic Analysis
10.1039/d1cy01219c · ExternalCitation · doi-reference
Photoredox Catalytic Deoxygenative Divergent Functionalizations of Alcohols Assisted by N,O-Heterocyclic Carbenes
10.1039/d4qo00115j · ExternalCitation · doi-reference
Electrochemical Synthesis of Aziridines, Pyrrolidines and Oxazolines Enabled by Azo-Free Alcohol Amination
10.1039/d5sc03101j · ExternalCitation · doi-reference
A New Method for the Deoxygenation of Secondary Alcohols
10.1039/p19750001574 · ExternalCitation · doi-reference
Electro-Organic Reactions. Part 1. The Cathodic Cleavage in Methanol Solution of Benzylic Carbon-Oxygen and Carbon-Fluorine Bonds
10.1039/p29730001903 · ExternalCitation · doi-reference
Some Applications of the Transition State Method to the Calculation of Reaction Velocities, Especially in Solution
10.1039/tf9353100875 · ExternalCitation · doi-reference
Titanium: A Unique Metal for Radical Dehydroxylative Functionalization of Alcohols
10.1055/a-1406-0484 · ExternalCitation · doi-reference
Recent Progress on Transition-Metal-Mediated Reductive C(Sp3)–O Bond Radical Addition and Coupling Reactions
10.1055/a-1848-3005 · ExternalCitation · doi-reference
Unlocking C–OH Bond Activation for Radical C-Glycosylation of Native Saccharides
10.1055/a-2572-0983 · ExternalCitation · doi-reference
Electrochemical Deoxygenation of Primary Alcohols
10.1055/s-0031-1290778 · ExternalCitation · doi-reference
Boryl Radical-Promoted Deoxygenative Alkylation of Benzyl Acetates
10.1055/s-0042-1751463 · ExternalCitation · doi-reference
Redox-Neutral Organocatalytic Mitsunobu Reactions
10.1126/science.aax3353 · ExternalCitation · doi-reference
Progress of the Barton-McComble Methodology: From Tin Hydrides to Silanes
10.1163/156856793x00361 · ExternalCitation · doi-reference
Preparation of Esters of Phosphoric Acid by the Reaction of Trivalent Phosphorus Compounds with Diethyl Azodicarboxylate in the Presence of Alcohols
10.1246/bcsj.40.935 · ExternalCitation · doi-reference
Tin-Free Alternatives to the Barton-McCombie Deoxygenation of Alcohols to Alkanes Involving Reductive Electron Transfer
10.2533/chimia.2016.67 · ExternalCitation · doi-reference