Abstract
Bin Xia Zhao, Jia-Yi Shang, Guo-Qin Hu, Jing‐Hui Liu
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Progress on the Transition Metal-catalyzed Cross-coupling Reaction of Thioesters
10.6023/a23010013 · 2023
Predicting the reaction mechanism of nucleophilic substitutions at carbonyl and thiocarbonyl centres of esters and thioesters
10.1002/poc.3048 · 2012
Understanding the Relative Acyl-Transfer Reactivity of Oxoesters and Thioesters: Computational Analysis of Transition State Delocalization Effects
10.1021/ja010726a · 2001
N-Thiohydroxy Succinimide Esters (NTSEs): Versatile Reagents for Selective Acyl and Acylthio Transfer
10.1021/acs.orglett.2c02160 · 2022
Thioester Ligation with AAHO Peptides
10.1021/acs.orglett.5c04144 · 2025
Palladium-Catalyzed Thiocarbonylation of Aryl, Vinyl, and Benzyl Bromides
10.1021/jo5009965 · 2014
Thioester-mediated biocatalytic amide bond synthesis with in situ thiol recycling
10.1038/s41929-022-00889-x · 2023
Nickel-Catalyzed Cross-Coupling of Aziridines with Thioesters toward Atom-Economic Synthesis of β-Sulfanyl Amides
10.1021/acs.orglett.4c02823 · 2024
Pd-Catalyzed Thiocarbonylation with Stoichiometric Carbon Monoxide: Scope and Applications
10.1021/ol400138m · 2013
Enamides Accessed from Aminothioesters via a Pd(0)-Catalyzed Decarbonylative/β-Hydride Elimination Sequence
10.1021/ol101620r · 2010
Copper(II)-Catalyzed Reactions of α-Keto Thioesters with Azides via C–C and C–S Bond Cleavages: Synthesis of N-Acylureas and Amides
10.1021/acs.joc.7b03054 · 2018
Decarbonylative thioetherification by nickel catalysis using air- and moisture-stable nickel precatalysts
10.1039/c8cc00271a · 2018
Palladium- and Nickel-Catalyzed Decarbonylative C–S Coupling to Convert Thioesters to Thioethers
10.1021/acs.orglett.7b03305 · 2018
Rh(I)-Catalyzed Intramolecular Decarbonylation of Thioesters
10.1021/acs.joc.1c01117 · 2021
Forging C–S Bonds Through Decarbonylation: New Perspectives for the Synthesis of Privileged Aryl Sulfides
10.1002/cctc.202101206 · 2021
Controlled Ni-catalyzed mono- and double-decarbonylations of α-ketothioesters
10.1039/c8cc09352k · 2019
Decarbonylation of thiol esters to give sulfides promoted by transition metal complexes
10.1016/s0040-4039(01)91363-2 · 1987
One-Pot Synthesis of Symmetrical and Unsymmetrical Aryl Sulfides by Pd-Catalyzed Couplings of Aryl Halides and Thioacetates
10.1021/jo2007253 · 2011
A Prototype of Transition-Metal-Catalyzed Carbothiolation of Alkynes
10.1021/ja010261o · 2001
Divergent Acyl and Decarbonylative Liebeskind–Srogl Cross-Coupling of Thioesters by Cu-Cofactor and Pd–NHC (NHC = N-Heterocyclic Carbene) Catalysis
10.1021/acscatal.2c05550 · 2023
Decarboxylative Acylation of Carboxylic Acids: Reaction Investigation and Mechanistic Study
10.31635/ccschem.021.202101197 · 2022
Decarbonylative Liebeskind–Srogl Reductive Pyridination of Aromatic Thioesters by Cobalt Catalysis
10.1021/acs.orglett.5c02692 · 2025
Nickel-catalyzed cross-electrophile-coupling of thioesters with alkyl bromides to form ketones under mechanochemical conditions
10.1039/d6cc00297h · 2026
Synthesis and Base-Pairing Properties of Oligonucleotides Containing 5′-(R)- and 5′-(S)-C-Aryl-thymidine
10.1021/acs.joc.5c00641 · 2025
Ketone Synthesis under Neutral Conditions. Cu(I) Diphenylphosphinate-Mediated, Palladium-Catalyzed Coupling of Thiol Esters and Organostannanes
10.1021/ol034962x · 2003
A New Paradigm for Carbon–Carbon Bond Formation: Aerobic, Copper-Templated Cross-Coupling
10.1021/ja074931n · 2007
Cleavage of the C(O)–S Bond of Thioesters by Palladium/Norbornene/Copper Cooperative Catalysis: An Efficient Synthesis of 2-(Arylthio)aryl Ketones
10.1021/jacs.6b02495 · 2016
Catalytic Hydrogenation of Thioesters, Thiocarbamates, and Thioamides
10.1021/jacs.0c10884 · 2020
The Lyngbyatoxin Biosynthetic Assembly Line: Chain Release by Four-Electron Reduction of a Dipeptidyl Thioester to the Corresponding Alcohol
10.1021/ja077374d · 2007
Recent advances in Norrish–Yang cyclization and dicarbonyl photoredox reactions for natural product synthesis
10.3762/bjoc.21.177 · 2025
Biocompatible metal-assisted C–C cross-coupling combined with biocatalytic chiral reductions in a concurrent tandem cascade
10.1039/c8cc05304a · 2018
Mechanistic Investigations of Ruthenium Catalyzed Dehydrogenative Thioester Synthesis and Thioester Hydrogenation
10.1021/acscatal.1c00418 · 2021
Formation of thioesters by dehydrogenative coupling of thiols and alcohols with H2 evolution
10.1038/s41929-020-00514-9 · 2020
Fukuyama Reduction and Integrated Thioesterification/Fukuyama Reduction of Thioesters and Acyl Chlorides Using Continuous Flow
10.1021/cs5004917 · 2014
Facile reduction of ethyl thiol esters to aldehydes: application to a total synthesis of (+)-neothramycin A methyl ether
10.1021/ja00175a043 · 1990
Synthesis of conjugated multiunsaturated thioesters via one-pot TiCl4-promoted aldol condensation
10.1016/j.tetlet.2020.152280 · 2020
Palladium-Catalyzed Coupling of Thiol Esters with Aryl and Primary and Secondary Alkyl Organoindium Reagents
10.1021/jo050110u · 2005
In/I2 mediated functional group transformation: a direct approach toward the selective conversion of dithioester to ester
10.1016/j.tetlet.2015.08.035 · 2015
Facile Conversion of Dithioesters into Carboxylic Acids or Esters Using Alkaline Hydrogen Peroxide
10.1055/s-0028-1083190 · 2008
Facile synthesis of sulfinate esters from aryl iodides via direct oxidation of thioesters
10.1039/d3ob01108a · 2023
Photocatalytic Defluoroalkylation of Trifluoroacetates with Alkenes using 4-(Acetamido)thiophenol
10.1055/a-2019-1532 · doi-reference
Catalyst-Free Decarboxylation and Decarboxylative Giese Additions of Alkyl Carboxylates through Photoactivation of Electron Donor-Acceptor Complex
10.1002/adsc.201900803 · doi-reference
Triphenylphosphine-Catalyzed Alkylative Iododecarboxylation with Lithium Iodide under Visible Light
10.1021/acs.orglett.0c03173 · doi-reference
Photocatalytic Decarboxylative Alkylations of C(sp3)–H and C(sp2)–H Bonds Enabled by Ammonium Iodide in Amide Solvent
10.1007/s11426-020-9905-1 · doi-reference
Photocatalytic Decarboxylative Alkylations Mediated by Triphenylphosphine and Sodium Iodide
10.1126/science.aav3200 · doi-reference
Thiol-free arene C–H thioesterification enabled by a photoactive electron donor–acceptor complex
10.1039/d5sc05002b · doi-reference
Divergent Synthesis of Thioethers and Thioesters from Arenes and Carboxylic Acids
10.1021/acs.orglett.6c01581 · doi-reference
Recent Advances in Organic Reactions Involving Elemental Sulfur
10.1002/adsc.201601329 · doi-reference
Thianthrenium-enabled sulfonylation via electron donor-acceptor complex photoactivation
10.1016/j.checat.2022.03.007 · doi-reference
A general arene C–H functionalization strategy via electron donor–acceptor complex photoactivation
10.1038/s41557-022-01092-y · doi-reference
Visible-Light-Driven Synthesis of Aryl Xanthates and Aryl Dithiocarbamates via an Electron Donor–Acceptor Complex
10.1021/acs.orglett.2c03736 · doi-reference
A general electron donor–acceptor complex for photoactivation of arenes via thianthrenation
10.1039/d2sc01241c · doi-reference
BINOLates as Potent Reducing Photocatalysts for Inert-Bond Activation and Reduction of Unsaturated Systems
10.1016/j.chempr.2024.10.026 · doi-reference
Nickel Phosphite/Phosphine-Catalyzed C–S Cross-Coupling of Aryl Chlorides and Thiols
10.1021/acs.orglett.7b03560 · doi-reference
Thiyl Radical Trapped by Cobalt Catalysis: An Approach to Markovnikov Thiol–Ene Reaction
10.1021/acs.orglett.3c03740 · doi-reference
Ni-Catalyzed Aryl Sulfide Synthesis through an Aryl Exchange Reaction
10.1021/jacs.1c04215 · doi-reference
Neutralizing the Detrimental Effect of Glutathione on Precious Metal Catalysts
10.1021/ja500613n · doi-reference
Oxalic Acid Monothioester for Palladium-Catalyzed Decarboxylative Thiocarbonylation and Hydrothiocarbonylation
10.1021/acs.orglett.9b03701 · doi-reference
Palladium-Catalyzed Linear Hydrothiocarbonylation of Unactivated Terminal Alkenes: Synthesis of Aliphatic Thioesters
10.1021/acs.orglett.1c00406 · doi-reference
Palladium-Catalyzed Thiocarbonylative Synthesis of α,β-Unsaturated Thioesters Using S-Aryl Thioformates as the Thioester Sources
10.1021/acs.orglett.3c01400 · doi-reference
Nickel-Catalyzed Reductive Aryl Thiocarbonylation of Alkene via Thioester Group Transfer Strategy
10.1021/acs.orglett.0c02091 · doi-reference
Highly Regioselective Thiocarbonylation of Conjugated Dienes via Palladium-Catalyzed Three-Component Coupling Reactions
10.1021/jo000231o · doi-reference
Highly Regioselective Palladium-Catalyzed Thiocarbonylation of Allenes with Thiols and Carbon Monoxide
10.1021/jo972121w · doi-reference
Palladium-Catalyzed Thiocarbonylation of Aryl Iodides with S-Aryl Thioformates via Thioester Transfer
10.1021/acs.orglett.2c02953 · doi-reference
Palladium-Catalyzed Thiocarbonylation of Alkenes toward Linear Thioesters
10.1021/acscatal.1c00414 · doi-reference
Photoredox mediated nickel catalyzed C(sp3)–H thiocarbonylation of ethers
10.1039/c7sc02516e · doi-reference
Pentafluorophenylammonium triflate (PFPAT): an efficient, practical, and cost-effective catalyst for esterification, thioesterification, transesterification, and macrolactone formation
10.1039/b609181b · doi-reference
Methanesulfonic anhydride-promoted sustainable synthesis of thioesters from feedstock acids and thiols
10.1007/s12039-020-01871-5 · doi-reference
Pummerer-type Cyclization of Arnstein Tripeptide Analogs Induced by O-Silylated Ketene Acetals: Studies of Penicillin Biosynthesis
10.1021/ja00091a013 · doi-reference
Biocatalytic cyclization of small macrolactams by a penicillin-binding protein-type thioesterase
10.1038/s41589-023-01495-z · doi-reference
Penicillin biosynthesis: intermediates of biosynthesis of δ-l-α-aminoadipyl-l-cysteinyl-d-valine formed by ACV synthetase from Acremonium chrysogenum
10.1016/s0014-5793(97)00977-0 · doi-reference
Highly Stereoselective Diels–Alder-Based Strategy for the Synthesis of 3-epi-Formicin A and 1-epi-Formicin B
10.1021/acs.orglett.4c01209 · doi-reference
Formicins, N-Acetylcysteamine-Bearing Indenone Thioesters from a Wood Ant-Associated Bacterium
10.1021/acs.orglett.0c01584 · doi-reference
Biodegradable and Stimuli-Responsive Nanomaterials for Targeted Drug Delivery in Autoimmune Diseases
10.3390/jfb16010024 · doi-reference
Recyclable Polythioesters and Poly(thioester-co-peptoid)s via Ring-Opening Cascade Polymerization of Amino Acid N-Carboxyanhydrides
10.1002/anie.202411630 · doi-reference
The structure of the monobactam-producing thioesterase domain of SulM forms a unique complex with the upstream carrier protein domain
10.1016/j.jbc.2024.107489 · doi-reference
The S-Thioester Enolate/Imine Condensation: A Shortcut to β-Lactams
10.1002/(sici)1099-0690(200002)2000:4<563::aid-ejoc563>3.0.co;2-m · doi-reference
The Asymmetric Addition of the Sn(II) Enolates of Thioesters to α-Iminoesters. A Convenient Synthesis of Optically Active cis-Substituted β-Lactams
10.1246/cl.1987.293 · doi-reference
Probing biosynthesis of plant polyketides with synthetic N-acetylcysteamine thioesters
10.1016/j.bbrc.2004.10.057 · doi-reference
Recent achievements on the agricultural applications of thioether derivatives: A 2010–2020 decade in review
10.1002/jhet.4234 · doi-reference