References

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 · ExternalCitation · doi-reference

Recent Advances in Organic Reactions Involving Elemental Sulfur

10.1002/adsc.201601329 · ExternalCitation · doi-reference

Catalyst-Free Decarboxylation and Decarboxylative Giese Additions of Alkyl Carboxylates through Photoactivation of Electron Donor-Acceptor Complex

10.1002/adsc.201900803 · ExternalCitation · doi-reference

A Mild Method for Access to α-Substituted Dithiomalonates through C-Thiocarbonylation of Thioester: Synthesis of Mesoionic Insecticides

10.1002/adsc.202100369 · ExternalCitation · doi-reference

Recyclable Polythioesters and Poly(thioester-co-peptoid)s via Ring-Opening Cascade Polymerization of Amino Acid N-Carboxyanhydrides

10.1002/anie.202411630 · ExternalCitation · doi-reference

Forging C–S Bonds Through Decarbonylation: New Perspectives for the Synthesis of Privileged Aryl Sulfides

10.1002/cctc.202101206 · ExternalCitation · doi-reference

Recent achievements on the agricultural applications of thioether derivatives: A 2010–2020 decade in review

10.1002/jhet.4234 · ExternalCitation · doi-reference

Predicting the reaction mechanism of nucleophilic substitutions at carbonyl and thiocarbonyl centres of esters and thioesters

10.1002/poc.3048 · ExternalCitation · 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 · ExternalCitation · doi-reference

Methanesulfonic anhydride-promoted sustainable synthesis of thioesters from feedstock acids and thiols

10.1007/s12039-020-01871-5 · ExternalCitation · doi-reference

Probing biosynthesis of plant polyketides with synthetic N-acetylcysteamine thioesters

10.1016/j.bbrc.2004.10.057 · ExternalCitation · doi-reference

Thianthrenium-enabled sulfonylation via electron donor-acceptor complex photoactivation

10.1016/j.checat.2022.03.007 · ExternalCitation · doi-reference

BINOLates as Potent Reducing Photocatalysts for Inert-Bond Activation and Reduction of Unsaturated Systems

10.1016/j.chempr.2024.10.026 · ExternalCitation · 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 · ExternalCitation · doi-reference

Design, synthesis, and insecticidal activities of novel thioether derivatives

10.1016/j.molstruc.2025.144228 · ExternalCitation · doi-reference

In/I2 mediated functional group transformation: a direct approach toward the selective conversion of dithioester to ester

10.1016/j.tetlet.2015.08.035 · ExternalCitation · doi-reference

Synthesis of conjugated multiunsaturated thioesters via one-pot TiCl4-promoted aldol condensation

10.1016/j.tetlet.2020.152280 · ExternalCitation · 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 · ExternalCitation · doi-reference

The reaction of thioesters with nitriles. A new synthetic approach to the preparation of substituted 4-alkylthio- and 4-arylthiopyrimidine derivatives

10.1016/s0040-4020(03)01133-5 · ExternalCitation · doi-reference

Decarbonylation of thiol esters to give sulfides promoted by transition metal complexes

10.1016/s0040-4039(01)91363-2 · ExternalCitation · doi-reference

Rh(I)-Catalyzed Intramolecular Decarbonylation of Thioesters

10.1021/acs.joc.1c01117 · ExternalCitation · doi-reference

S-Arylation of Thioic S-Acid Using Thianthrenium Salts via Photoactivation of Electron Donor–Acceptor Complex

10.1021/acs.joc.4c01473 · ExternalCitation · doi-reference

Synthesis and Base-Pairing Properties of Oligonucleotides Containing 5′-(R)- and 5′-(S)-C-Aryl-thymidine

10.1021/acs.joc.5c00641 · ExternalCitation · doi-reference

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 · ExternalCitation · doi-reference

Poly(thioester) by Organocatalytic Ring-Opening Polymerization

10.1021/acs.macromol.5b01463 · ExternalCitation · doi-reference

Formicins, N-Acetylcysteamine-Bearing Indenone Thioesters from a Wood Ant-Associated Bacterium

10.1021/acs.orglett.0c01584 · ExternalCitation · doi-reference

Nickel-Catalyzed Reductive Aryl Thiocarbonylation of Alkene via Thioester Group Transfer Strategy

10.1021/acs.orglett.0c02091 · ExternalCitation · doi-reference

Triphenylphosphine-Catalyzed Alkylative Iododecarboxylation with Lithium Iodide under Visible Light

10.1021/acs.orglett.0c03173 · ExternalCitation · doi-reference

Palladium-Catalyzed Linear Hydrothiocarbonylation of Unactivated Terminal Alkenes: Synthesis of Aliphatic Thioesters

10.1021/acs.orglett.1c00406 · ExternalCitation · doi-reference

N-Thiohydroxy Succinimide Esters (NTSEs): Versatile Reagents for Selective Acyl and Acylthio Transfer

10.1021/acs.orglett.2c02160 · ExternalCitation · doi-reference

Palladium-Catalyzed Thiocarbonylation of Aryl Iodides with S-Aryl Thioformates via Thioester Transfer

10.1021/acs.orglett.2c02953 · ExternalCitation · doi-reference

Visible-Light-Driven Synthesis of Aryl Xanthates and Aryl Dithiocarbamates via an Electron Donor–Acceptor Complex

10.1021/acs.orglett.2c03736 · ExternalCitation · doi-reference

Palladium-Catalyzed Thiocarbonylative Synthesis of α,β-Unsaturated Thioesters Using S-Aryl Thioformates as the Thioester Sources

10.1021/acs.orglett.3c01400 · ExternalCitation · doi-reference

Thiyl Radical Trapped by Cobalt Catalysis: An Approach to Markovnikov Thiol–Ene Reaction

10.1021/acs.orglett.3c03740 · ExternalCitation · 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 · ExternalCitation · doi-reference

Nickel-Catalyzed Cross-Coupling of Aziridines with Thioesters toward Atom-Economic Synthesis of β-Sulfanyl Amides

10.1021/acs.orglett.4c02823 · ExternalCitation · doi-reference

Decarbonylative Liebeskind–Srogl Reductive Pyridination of Aromatic Thioesters by Cobalt Catalysis

10.1021/acs.orglett.5c02692 · ExternalCitation · doi-reference

Thioester Ligation with AAHO Peptides

10.1021/acs.orglett.5c04144 · ExternalCitation · doi-reference

Divergent Synthesis of Thioethers and Thioesters from Arenes and Carboxylic Acids

10.1021/acs.orglett.6c01581 · ExternalCitation · doi-reference

Palladium- and Nickel-Catalyzed Decarbonylative C–S Coupling to Convert Thioesters to Thioethers

10.1021/acs.orglett.7b03305 · ExternalCitation · doi-reference

Nickel Phosphite/Phosphine-Catalyzed C–S Cross-Coupling of Aryl Chlorides and Thiols

10.1021/acs.orglett.7b03560 · ExternalCitation · doi-reference

Oxalic Acid Monothioester for Palladium-Catalyzed Decarboxylative Thiocarbonylation and Hydrothiocarbonylation

10.1021/acs.orglett.9b03701 · ExternalCitation · doi-reference

Photo-Degradable Functional Polyesters from an o-Nitrobenzyl Dithiol: Synthesis and Applications in Herbicide Delivery

10.1021/acsapm.3c00719 · ExternalCitation · doi-reference

Palladium-Catalyzed Thiocarbonylation of Alkenes toward Linear Thioesters

10.1021/acscatal.1c00414 · ExternalCitation · doi-reference

Mechanistic Investigations of Ruthenium Catalyzed Dehydrogenative Thioester Synthesis and Thioester Hydrogenation

10.1021/acscatal.1c00418 · ExternalCitation · doi-reference

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 · ExternalCitation · doi-reference

Fukuyama Reduction and Integrated Thioesterification/Fukuyama Reduction of Thioesters and Acyl Chlorides Using Continuous Flow

10.1021/cs5004917 · ExternalCitation · doi-reference

Pummerer-type Cyclization of Arnstein Tripeptide Analogs Induced by O-Silylated Ketene Acetals: Studies of Penicillin Biosynthesis

10.1021/ja00091a013 · ExternalCitation · doi-reference

Facile reduction of ethyl thiol esters to aldehydes: application to a total synthesis of (+)-neothramycin A methyl ether

10.1021/ja00175a043 · ExternalCitation · doi-reference

A Prototype of Transition-Metal-Catalyzed Carbothiolation of Alkynes

10.1021/ja010261o · ExternalCitation · doi-reference

Understanding the Relative Acyl-Transfer Reactivity of Oxoesters and Thioesters: Computational Analysis of Transition State Delocalization Effects

10.1021/ja010726a · ExternalCitation · doi-reference

A New Paradigm for Carbon–Carbon Bond Formation: Aerobic, Copper-Templated Cross-Coupling

10.1021/ja074931n · ExternalCitation · doi-reference

The Lyngbyatoxin Biosynthetic Assembly Line: Chain Release by Four-Electron Reduction of a Dipeptidyl Thioester to the Corresponding Alcohol

10.1021/ja077374d · ExternalCitation · doi-reference

Neutralizing the Detrimental Effect of Glutathione on Precious Metal Catalysts

10.1021/ja500613n · ExternalCitation · doi-reference

Catalytic Hydrogenation of Thioesters, Thiocarbamates, and Thioamides

10.1021/jacs.0c10884 · ExternalCitation · doi-reference

Ni-Catalyzed Aryl Sulfide Synthesis through an Aryl Exchange Reaction

10.1021/jacs.1c04215 · ExternalCitation · doi-reference

Diaryl Ether Formation by a Versatile Thioesterase Domain

10.1021/jacs.2c02813 · ExternalCitation · doi-reference

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 · ExternalCitation · doi-reference

Highly Regioselective Thiocarbonylation of Conjugated Dienes via Palladium-Catalyzed Three-Component Coupling Reactions

10.1021/jo000231o · ExternalCitation · doi-reference

Palladium-Catalyzed Coupling of Thiol Esters with Aryl and Primary and Secondary Alkyl Organoindium Reagents

10.1021/jo050110u · ExternalCitation · doi-reference

One-Pot Synthesis of Symmetrical and Unsymmetrical Aryl Sulfides by Pd-Catalyzed Couplings of Aryl Halides and Thioacetates

10.1021/jo2007253 · ExternalCitation · doi-reference

Palladium-Catalyzed Thiocarbonylation of Aryl, Vinyl, and Benzyl Bromides

10.1021/jo5009965 · ExternalCitation · doi-reference

Highly Regioselective Palladium-Catalyzed Thiocarbonylation of Allenes with Thiols and Carbon Monoxide

10.1021/jo972121w · ExternalCitation · doi-reference

A Short Stereoselective Total Synthesis of the Fusarium Toxin Equisetin

10.1021/ol006493u · ExternalCitation · doi-reference

Ketone Synthesis under Neutral Conditions. Cu(I) Diphenylphosphinate-Mediated, Palladium-Catalyzed Coupling of Thiol Esters and Organostannanes

10.1021/ol034962x · ExternalCitation · doi-reference

Enamides Accessed from Aminothioesters via a Pd(0)-Catalyzed Decarbonylative/β-Hydride Elimination Sequence

10.1021/ol101620r · ExternalCitation · doi-reference

Pd-Catalyzed Thiocarbonylation with Stoichiometric Carbon Monoxide: Scope and Applications

10.1021/ol400138m · ExternalCitation · doi-reference

A general arene C–H functionalization strategy via electron donor–acceptor complex photoactivation

10.1038/s41557-022-01092-y · ExternalCitation · doi-reference

Biocatalytic cyclization of small macrolactams by a penicillin-binding protein-type thioesterase

10.1038/s41589-023-01495-z · ExternalCitation · doi-reference

Formation of thioesters by dehydrogenative coupling of thiols and alcohols with H2 evolution

10.1038/s41929-020-00514-9 · ExternalCitation · doi-reference

Thioester-mediated biocatalytic amide bond synthesis with in situ thiol recycling

10.1038/s41929-022-00889-x · ExternalCitation · doi-reference

Pentafluorophenylammonium triflate (PFPAT): an efficient, practical, and cost-effective catalyst for esterification, thioesterification, transesterification, and macrolactone formation

10.1039/b609181b · ExternalCitation · doi-reference

Photoredox mediated nickel catalyzed C(sp3)–H thiocarbonylation of ethers

10.1039/c7sc02516e · ExternalCitation · doi-reference

Decarbonylative thioetherification by nickel catalysis using air- and moisture-stable nickel precatalysts

10.1039/c8cc00271a · ExternalCitation · doi-reference

Biocompatible metal-assisted C–C cross-coupling combined with biocatalytic chiral reductions in a concurrent tandem cascade

10.1039/c8cc05304a · ExternalCitation · doi-reference

Controlled Ni-catalyzed mono- and double-decarbonylations of α-ketothioesters

10.1039/c8cc09352k · ExternalCitation · doi-reference

A general electron donor–acceptor complex for photoactivation of arenes via thianthrenation

10.1039/d2sc01241c · ExternalCitation · doi-reference

Facile synthesis of sulfinate esters from aryl iodides via direct oxidation of thioesters

10.1039/d3ob01108a · ExternalCitation · doi-reference

Visible light-induced sulfonylation reaction of copper-catalyzed thianthrenium salts

10.1039/d5cc06985h · ExternalCitation · doi-reference

Thiol-free arene C–H thioesterification enabled by a photoactive electron donor–acceptor complex

10.1039/d5sc05002b · ExternalCitation · doi-reference

Nickel-catalyzed cross-electrophile-coupling of thioesters with alkyl bromides to form ketones under mechanochemical conditions

10.1039/d6cc00297h · ExternalCitation · doi-reference

Photocatalytic Defluoroalkylation of Trifluoroacetates with Alkenes using 4-(Acetamido)thiophenol

10.1055/a-2019-1532 · ExternalCitation · doi-reference

Facile Conversion of Dithioesters into Carboxylic Acids or Esters Using Alkaline Hydrogen Peroxide

10.1055/s-0028-1083190 · ExternalCitation · doi-reference

Photocatalytic Decarboxylative Alkylations Mediated by Triphenylphosphine and Sodium Iodide

10.1126/science.aav3200 · ExternalCitation · doi-reference

Activation parameters of the reactions of 4-nitrophenyl benzoates and S-phenyl benzothioate with 4-chlorophenol in dimethylformamide in the presence of potassium carbonate

10.1134/s1070428009040095 · ExternalCitation · 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 · ExternalCitation · doi-reference

Synthesis of Acylsilanes by Palladium-catalyzed Cross-coupling Reaction of Thiol Esters and Silylzinc Chlorides

10.1246/cl.2011.959 · ExternalCitation · doi-reference

Design, Synthesis, and Insecticidal Activities of Novel Thioether and Oxide Sulfide-containing Diamide Compounds

10.2174/1570180820666221115143850 · ExternalCitation · doi-reference

Decarboxylative Acylation of Carboxylic Acids: Reaction Investigation and Mechanistic Study

10.31635/ccschem.021.202101197 · ExternalCitation · doi-reference

Biodegradable and Stimuli-Responsive Nanomaterials for Targeted Drug Delivery in Autoimmune Diseases

10.3390/jfb16010024 · ExternalCitation · doi-reference

Recent advances in Norrish–Yang cyclization and dicarbonyl photoredox reactions for natural product synthesis

10.3762/bjoc.21.177 · ExternalCitation · doi-reference

Progress on the Transition Metal-catalyzed Cross-coupling Reaction of Thioesters

10.6023/a23010013 · ExternalCitation · doi-reference