SEARCH Articles Figures Tables 1,3,4-Oxadiazolium-thiolat 1.3- Dithiole-2-thione-4,5-thiolate 1.3.4- Oxadiazolium 2-thiolates 1.3.4- Thiadiazolium-2-thiolates 2-Iminothiolane thiolation 2-Iminothiolane toxin thiolation using 5-Allyl thiolates, synthesis 6- -pyridine-2-thiolate A-Thiolation A-Thiolation difunctionalization Adsorbed thiolates Alkali-metal thiolates Alkylation thiolate-bridged diruthenium Alkylmagnesium thiolates Aluminum thiolates, dialkylBeckmann rearrangement Amide, thiolate, and alkoxide ligands Amides, Alkoxides and Thiolates Amido/thiolate complexes Anions thiolates Antibodies thiolation Aqueous reactions thiolate-containing ligands Arene thiolates, reaction with halogen Arene thiolation Arenes thiolation Aryl thiolation Avidin thiolation Benzothiazole-2-thiolate Biocatalyst heme-thiolate haloperoxidases Bismuth thiolate complexes Bond lengths thiolate complexes Bond lengths thiolates CESIUM THIOLATES Cadmium thiolate Cadmium thiolates Cadmium, thiolate complexes 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Nickel thiolates Nickel thiolates electronic structure Nucleophilic substitution with thiolates Of coordinated thiolate Of coordinated thiolates Oligo thiolate Organoaluminum thiolates Organotin thiolates Organozinc thiolates Osmium complexes thiolates Osmium, thiolate complexes Oxatriazolium-5-thiolates Oxygen thiolate complexes Palladium complexes thiolates Palladium thiolate complexes Palladium thiolates, reactions with Phosphine thiolate complexes Phosphino-thiolate ligands Phosphonium thiolate Phosphonium thiolates, reactions Physical Properties of Cd(II) in Thiolate Proteins Platinum, thiolate complexes Polysaccharide thiolation using PDPH Protein S-thiolation signal or damage Protein oxidation thiolation Protein thiolated Pseudomonas toxin thiolation with 2iminothiolane Reactions of Co-ordinated Thiolate Reactivity of Thiolate Complexes Reduction potentials thiolate complexes Reduction thiolate substitution Rhenium, thiolate complexes Ruthenium complexes thiolates Ruthenium, 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Thiolate sterically hindered Thiolate structures Thiolate substitution reactions Thiolate substitutions Thiolate syntheses Thiolate transition metal complexes Thiolate-Containing Ligands Thiolate-Ligated Heme Systems Thiolate-alkylating enzyme Thiolate-bridged diruthenium Thiolate-bridged diruthenium complexes Thiolate-copper complexes Thiolate-gold® complexes luminescence Thiolate-ligated catalysts Thiolated chitosan, mucoadhesive potentials Thiolated cyclodextrins Thiolated dextran Thiolated heparin Thiolated monolayers Thiolated poly polymer Thiolated polycarbophil Thiolated polymers Thiolated ssDNA Thiolates Thiolates Thiolates 1,3-cycloaddition, anionic Thiolates Schiff base complexes Thiolates Subject Thiolates Thiols Thiolates This page has been reformatted by Knovel to provide easier navigation Thiolates a-alkylthiocarbonyl compounds Thiolates aggregate metal complexes Thiolates and thioethers Thiolates arylthiolates Thiolates bonding Thiolates bridging ligands Thiolates cluster chemistry Thiolates conversion Thiolates cross-coupling Thiolates dinuclear complexes Thiolates homoleptic, metal complexes Thiolates metal complexes Thiolates metallothioneins Thiolates mixed ligand complexes Thiolates molecular synthesis Thiolates monodentate Thiolates monodentate metal complexes Thiolates mononuclear complexes Thiolates organometallics Thiolates physical properties Thiolates polydentate Thiolates polynuclear complexes Thiolates reactions Thiolates reduction Thiolates sterically hindered Thiolates synthesis Thiolates terminal ligands Thiolates thermolysis Thiolates thiosulfates Thiolates triazine Thiolates triazole Thiolates tridentate Thiolates tris Thiolates uranium Thiolates ureas Thiolates with aluminum Thiolates xanthates Thiolates, group Thiolates, molybdenum enzymes Thiolates, oxidation Thiolates, patterning SAMs Thiolates, reactions, carbon disulfide Thiolates, replacement Thiolating reagents Thiolating review Thiolation Thiolation Thiolation N-acetyl 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