SEARCH Articles Figures Tables 1,1-DithioIs 1.3- dithioles 1,1-Dithiolate ligands 1,2-Dicyanoethylene-1,2-dithiolate ligand 1,2-Dithiole-3-thione, methylation 1,2-Maleonitrile 1,2-dithiolate ligands 1,2-Maleonitrile 1,2-dithiolate ligands ligand structures 1,3,4-Thiadiazole-2,5-dithiol 1,3-Dithioles, mesoionic 1,3-Dithioles, oxidative coupling 1.1- Dithiolate derivatives, sulfur 1.1- Dithiolate derivatives, sulfur addition 1.1- Dithiolates, reaction chemistry 1.1- dicyanoethylene-2,2-dithiolate 1.2- Dithiol-3-imines, reaction with 1.2- Dithiol-3-ones 1.2- Dithiol-3-ones reaction with Grignard reagents 1.2- Dithiol-3-ones spectra 1.2- Dithiol-3-thiones 1.2- Dithiolanes 1.3- dithiols 1.2- Dithiole-3-oncs 1.2- Dithiole-3-ones, ring opening 1.2- Dithiole-3-thione, calculated vibrational 1.2- Dithiole-3-thiones 1.2- Dithiole-3-thiones 1.2- dithiolium salts 1.2- Dithiole-3-thiones and 1,2-dithiol 1.2- Dithiole-3-thiones and 1,2-dithiol-3-ones 1.2- Dithiole-3-thiones and 1,2-dithiol3-ones 1.2- Dithiole-3-thiones and l,2-dithiol-3-ones 1.2- Dithiole-3-thiones conductivity 1.2- Dithiole-3-thiones ketones 1.2- Dithiole-3-thiones metal complexes 1.2- Dithiole-3-thiones oxidation 1.2- Dithiole-3-thiones reactions 1.2- Dithiole-3-thiones reduction 1.2- Dithiole-3-thiones ring transformations 1.2- Dithiole-3-thiones spectra 1.2- Dithiole-3-thiones structure 1.2- Dithiole-3-thiones synthesis 1.2- Dithiole-3-thiones with benzyne 1.2- Dithiole-3-thiones with carbene precursors 1.2- Dithiole-3-thiones, reaction with 1.2- Dithioles 1.2- Dithioles dihydro 1.2- Dithioles hydrocarbons 1.2- Dithioles intermediates 1.2- Dithioles radicals from 1.2- Dithioles reaction with acetylenic esters 1.2- Dithioles special 1.2- Dithioles tautomerism 1.2- Dithioles, 3- photochemistry 1.2- Dithioles, intramolecular charge transfer 1.2- Dithiols cyclic 1.2- dithiol 1.3- Dithiol, 2,2-dibenzyl-4-phenyl 1.3- Dithiol-2-ylidene 1.3- Dithiol-4-olates 1.3- Dithiole-2-azide 1.3- Dithiole-2-iminium salts 1.3- Dithiole-2-phosphonates 1.3- Dithiole-2-thione 1.3- Dithiole-2-thione, chlorination 1.3- Dithiole-2-thione-4,5-dithiolato 1.3- Dithiole-2-thione-4,5-thiolate 1.3- Dithiole-2-thiones acetylene derivatives 1.3- Dithioles 1,1-dithiols 1.3- Dithioles 1.3- dithiolium salts 1.3- Dithioles 1.4- dithiafulvenes 1.3- Dithioles 2-alkoxy- from 1.3- Dithioles, 2- preparation, structure 1.3- Dithiols thietanes 1.3- Dithiols, oxidative cyclization 1.3- Dithole-2-thione-4,5-dithiolate anion vibration frequencies 1.3- dithiol-2-ylidene compounds 1.4- Dithiols dithiothreitol 1.4- Dithiols specials 13-Dipolar cycloaddition 1.2- Dithioles 13-Dithiolium - from 1.3- dithioles, 2-amino 2- -l,3-dithiols 2-thioxo-1,3-dithioles (also 1,3-dithiole 3,6-Dichlorobenzene-1,2-dithiolate 3-Alkylidene-l,2-dithioles 3-Imino-l,2-dithioles 3H -1,2-Dithiol-3-ones 3H-1,2-Dithiole 3H-l,2-Dithiole-3-thiones 3H-l,2-dithiol-3-thione 4,5-Dimercapto-1,3-dithiole-2-thione (dmit 4,5-Ethylenedithio-1,3-dithiole-2-thione 4,5-Ethylenedithio-l,3-dithiole-2-thione 4.5- Disulfanyl-l,3-dithiole-2-thionate 4.5- dicyano-l,3-dithiol-2-one Acetonides to protect dithiols Aldehydes dithiol acetals Aldehydes reaction with dithiols Alkene dithiolates Arsen-1,1-dithiolates Benzene Dithiol An Exemplary Case Benzene dithiol Benzene dithiol conductance Benzo dithiol-3-thione Benzo-1,3-dithiole-2-thiones Benzo-1,3-dithiole-2-thiones reduction Benzo-l,2-dithiole-3-thione Benzo-l,3-dithiol-2-thione Binaphthalene-2,2-dithiol Bridge, dithiolate Cadmium dithiol complexes Cadmium dithiolate Carborane-dithiolate ligand Cobalt complexes 1.2- dithiolates Cobalt complexes dithiolate Copper complexes 1,1-dithiolates Cyclic lead dithiolates, polymeric Cyclopentadienyl dithiolate complexes Dicyanoethene-1,2-dithiol Dicyanoethylene dithiolate, isothiazoles Diimines mixed-ligand diimine dithiolates Diisocyanate Dithiol Dimeric 1,1-dithiolate Diorganotin dithiolates Dithianes from dithiols Dithiol catalysts Dithiol complexes Dithiol molecules Dithiol-4-imines Dithiolate Dithiolate Dithiolate complexes Dithiolate complexes reactions Dithiolate complexes structure Dithiolate complexes substitution reactions Dithiolate complexes sulfur-addition reaction Dithiolate complexes with Lewis acids Dithiolate diiron Dithiolate ions Dithiolate salt Dithiolate-based Z-selective catalysts Dithiolates Dithiolates 1,2-dithiolate-type, structure Dithiolates 4,5-dithiolato-1,3-dithiol-2-thione Dithiolates flotation Dithiolates formation Dithiolates integral oxidation state Dithiolates interactions Dithiolates metal complexes Dithiolates nomenclature Dithiolates non-integral oxidation state Dithiolates, geminal Dithiolates, lithium complexes Dithiolates, structure Dithiole Dithiole Dithiole Carbene Reactions and Bi-l,3-dithioles Dithiole Derivatives Dithiole Series Dithiole oxidative dimerization Dithiole-2-ones Dithiole-2-selenones Dithiole-2-thionate ligands, “redox Dithiole-2-thiones and Selenium-containing Analogues Dithiole-2-thiones rearrangement Dithioles and Related Compounds Dithioles and Related Systems Dithioles and dithiolanes Dithioles reduction Dithioles, synthesis Dithiols Dithiols Dithiols aldehydes Dithiols disulfides, cyclic Dithiols ethanedithiol Dithiols from alkenes Dithiols from carbonyl compounds Dithiols from disulfides Dithiols from imines Dithiols geminal Dithiols ketones Dithiols reaction with, phosgene Dithiols, formation Dithiols, from carbonyls Dithiols, polydisulfides Dithiols, protection Dithiols, radical addition Dithiols, reaction with lewisite Electron 1,2-dithiolates Ene-1,1-dithiols Ene-l,2-dithiolates Ethan-1,2-dithiol Ethane-1,2-dithiol Ethane-1,2-dithiolates Ethers, reaction with dithiols Ethylene-2,2-dithiolates Gem-Dithiols Gold complexes dithiolates Heterocyclic and Heteroatomic Dithiolates Hexane dithiol I, 2-Dithiole-3-thione Imino-l,2-dithiole Iron dithiolate complexes L,2-Dithiol-3 Ones L,2-Dithiol-3-one, calculated vibrational spectra L,2-Dithiole-3-thiones L,2-dithiole-3-one L,3-DITHIOLE-2-THIONE-4,5-DITHIOLATE L,3-DITHIOLE-2-THIONE-4,5-DITHIOLATE SALTS L,3-Dithiole-2-thione-4,5-dithiolate dmit) Lead dithiolates Lead dithiolates, cyclic— Maleonitrile dithiolate Manganese complexes dithiolates Mercaptans dithiols Mercury dithiol complexes Metal dithiolates Molybdenum complexes 1,1-dithiolate Naphthalene-1,5-dithiol Nickel dithiolate O-Dithiols Of dithiols Oxidation of l,2-dithiole-3-thiones Pedersen, C. Th., 1,2-Dithiole-3-thiones and Platinum complexes alkene-1,2-dithiolates Platinum diimine dithiolate Preparation of a-(l,2-Dithiol-3-ylidene)carbonyl Compounds Propane dithiol Propane-1,3-dithiol, reaction with aldehydes Pyridine-2,3-dithiol, reaction with 1-chloro2-nitrobenzene Quinoxaline-2,3-dithiol Quinoxaline-2,3-dithiol metal complexes Quinoxaline-2,3-dithiolate dianion Radical ring-opening with dithiols Radicals Containing a 1,2-Dithiole Ring S dithiolates Selenium dithiolates Silane-1,1-dithiolates Silane-1,1-dithiolates and Tin Analogs Silylated dithiols, with Spiro[ 1,3-dithiol-2,9’-fluorene TTF-dithiolate complexes TTF-dithiolate ligands Technetium complexes dithiol Tellurium Dithiolates Thieno -1,3-dithiole-2-thione Thiol-groups Dithiols Toluene dithiol complex Toluene-3,4-dithiol Toluene-3,4-dithiol metal complexes Toluene-3,4-dithiolate Triazine dithiol Vanadium complexes dithiolates Vicinal dithiols Zinc dithiol