SEARCH Articles Figures Tables 1, 2, 4, Thiadiazole diazonium salts 1, 2, 4, Thiadiazole diazonium salts coupling reactions 1, 2, 4, Thiadiazole diazonium salts from amino-1, 2, 4-thiadiazoles 1, 2, 4, Thiadiazole diazonium salts preparation 1, 2, 4, Thiadiazole diazonium salts with amines 1, 2, 4-Thiadiazole-5-sulfonic acids 1, 2, 4-Thiadiazole-carboxylates 1, 3, 4-Thiadiazoles, chemistry 1,2,3-Thiadiazole 4-carboxylic acid, ring synthesis 1,2,3-Thiadiazole Subject 1,2,3-Thiadiazole lithiation 1,2,3-Thiadiazole photolysis 1,2,3-Thiadiazole rearrangement 1,2,3-Thiadiazole thermolysis 1,2,3-Thiadiazoles Wolff rearrangement 1,2,3-Thiadiazoles flash-vacuum pyrolysis 1,2,3-Thiadiazoles synthesis of thioketenes 1,2,3-Thiadiazoles, elimination 1,2,3-Thiadiazoles, solution-phase 1,2,3-Thiadiazoles, synthesis using thionyl 1,2,3-Thiadiazoles, synthesis using thionyl chloride 1,2,3-thiadiazole 1,2,3-thiadiazole 1,2,3-thiadiazole, 4-carboxylic acid 1,2,4-Thiadiazole, 5-chloro-3-mercapto 1,2,5-Thiadiazole 1,1-dioxides structure 1,2,5-Thiadiazole 1,1-dioxides thermolysis 1,2,5-Thiadiazole 1-oxide 1,2,5-Thiadiazole ketones 1,2,5-Thiadiazole, 3-phenyl-, nitration 1,2,5-Thiadiazole-3,4-dicarbonyl 1,2,5-Thiadiazoles 1,2,5-Thiadiazoles 1,2,5-Thiadiazoles, aryl 1,3,4-Thiadiazole 2-dimethylamino 1,3,4-Thiadiazole 2-nitro-5-amino 1,3,4-Thiadiazole, 2-chloro-*, synthesis 1,3,4-Thiadiazole-2,5-dithiol 1,3,4-Thiadiazoles, 2-amino- from 1,3,4-Thiadiazoles, 2-amino-, EMME 1,3,4-thiadiazoles, microwave-assisted 1,3,4-thiadiazoles, microwave-assisted synthesis 1.2- Thiazolo -1,2,3-thiadiazole 1.2.3- Thiadiazole metallation 1.2.3- Thiadiazole, pyrolysis 1.2.3- Thiadiazole-4-carboxylic acid/ester 1.2.3- Thiadiazoles alkylation 1.2.3- Thiadiazoles deuteration 1.2.3- Thiadiazoles ring synthesis 1.2.3- Thiadiazoles, 5-azido 1.2.3- Thiadiazoles, alkyl-, side-chain 1.2.3- Thiadiazoles, base-catalyzed 1.2.3- Thiadiazoles, base-catalyzed exchange 1.2.3- Thiadiazoles, halo-, synthesis 1.2.3- Thiadiazoles, mesoionic 1.2.4- Oxadiazoles forming 1,2,4-thiadiazoles 1.2.4- Thiadiazol-5 -imines 1.2.4- Thiadiazole 1,1-dioxides, 4,5-dihydro 1.2.4- Thiadiazole 3-amino-, diazonium salts 1.2.4- Thiadiazole Dimroth rearrangements 1.2.4- Thiadiazole amino-, nitrosamines 1.2.4- Thiadiazole pyrimidine 1.2.4- Thiadiazole ring opening 1.2.4- Thiadiazole ring synthesis 1.2.4- Thiadiazole ring, functionalized 1.2.4- Thiadiazole, 5-amino-3-methyl 1.2.4- Thiadiazole, 5-amino-3-phenyl 1.2.4- Thiadiazole, ring expansion 1.2.4- Thiadiazole-3-thiones, tautomerism 1.2.4- Thiadiazoles 2 molecules) 1.2.4- Thiadiazoles biological properties 1.2.4- Thiadiazoles chemical properties 1.2.4- Thiadiazoles nitriles 1.2.4- Thiadiazoles physical properties 1.2.4- Thiadiazoles properties 1.2.4- Thiadiazoles ring interconversions 1.2.4- Thiadiazoles spectra 1.2.4- Thiadiazoles, 5-amino— from amidines 1.2.4- Thiadiazoles, amino-, halogenation 1.2.4- Thiadiazoles, formation rearrangements 1.2.4- Triazoles 1.3.4- thiadiazoles 1.2.4- Triazolo thiadiazoles 1.2.4- Triazolo thiadiazoles formation 1.2.5- Thiadiazol-3 -ones, synthesis 1.2.5- Thiadiazole .S’-oxide 1.2.5- Thiadiazole 1,1-dioxides 1.2.5- Thiadiazole 1,1-dioxides synthesis 1.2.5- Thiadiazole 3,4-dione 1.2.5- Thiadiazole anion radicals 1.2.5- Thiadiazole electrochemical reduction 1.2.5- Thiadiazole halogenation 1.2.5- Thiadiazole reduction 1.2.5- Thiadiazole reductive cleavage 1.2.5- Thiadiazole, 3-amino-, ring 1.2.5- Thiadiazole, 3-amino-, ring bromination 1.2.5- Thiadiazole, 3-methyl-, ring 1.2.5- Thiadiazole, chloromethylation 1.2.5- Thiadiazole-3,4-dicarbonitrile 1.2.5- Thiadiazoles 1.2- benzisothiazoles 1.2.5- Thiadiazoles 2,4-dihydro— from 1.2.5- Thiadiazoles hydrocarbons 1.2.5- Thiadiazoles stability 1.2.5- Thiadiazoles structural data 1.2.5- Thiadiazoles using 1.2.5- Thiadiazoles using thionyl chloride 1.2.5- Thiadiazoles, methyl-, side-chain 1.2.5- Thiadiazoles, reaction with 1.2.5- Thiadiazoles, synthesis 1.3.4- Thiadiazol-2-ones, mesoionic 1.3.4- Thiadiazole 2-amino-, bromination 1.3.4- Thiadiazole 2-chloro-, Dimroth rearrangement 1.3.4- Thiadiazole substituents, highly activated 1.3.4- Thiadiazole, 2-bromo 1.3.4- Thiadiazole, 2-bromo synthesis 1.3.4- Thiadiazole, 2-trichloromethyl 1.3.4- Thiadiazole, base-catalyzed 1.3.4- Thiadiazole, base-catalyzed exchange 1.3.4- Thiadiazoles basicity 1.3.4- Thiadiazoles review) 1.3.4- Thiadiazoles structure 1.3.4- Thiadiazoles tautomerism 1.3.4- Thiadiazoles, 2-chloro-, condensation 1.3.4- Thiadiazoles, amino-, diazotization 1.3.4- Thiadiazoles, recent advances 1.3.4- Thiadiazoles, recent advances in the 1.3.4- Thiadiazoles, recent advances in the chemistry 1.3.4- Thiadiazoles, substituted 1.3.4- thiadiazole-2-thiol 2, 5-Dimercapto-l, 3, 4-thiadiazole 2,5-Dimercapto-1,3,4-thiadiazole 2,5-Dimethyl-1,3,4-thiadiazole 2- Amino-1.3.4-thiadiazoles, acylation 2- Amino-l,3,4-thiadiazoles 2- Halo-1,3,4-thiadiazoles 2-Amino-1,3,4-thiadiazole 2-Amino-1,3,4-thiadiazoles, reaction with 2-Amino-5-aryl-1,3,4-thiadiazoles 2-Amino-5-ethyl-1,3,4-thiadiazole 2-Arylamino-l,3,4-thiadiazoles 2-Mercapto- 1,3,4-thiadiazoles, tautomerism 2-Mercapto-5-methyl-1,3,4-thiadiazole 2-Mercapto-5-methyl-l,3,4-thiadiazole 2-Mercapto-5-methyl-l,3,4-thiadiazole mercury complexes 2-Nitrosamino-13,4-thiadiazole 2.1.3- Thiadiazole ring 2.5- Diaryl-1,3,4-thiadiazoles 2.5- Dihydro-l ,3,4-thiadiazoles 2.5- dimercapto-l,3,4-thiadiazole DMcT) 3,4-Dicyano-l,2,5-thiadiazole 3- 1,2,5-thiadiazole 5,5-dioxide formation 3- Amino-1,2,5-thiadiazol, formation 3- Amino-1.2.5-thiadiazole, chlorination 3- Hydroxy-1,2,4-thiadiazoles 3- Hydroxy-1,2,4-thiadiazoles properties 3- Hydroxy-1,2,4-thiadiazoles synthesis 3- Hydroxy-1,2,4-thiadiazoles, tautomerism 3- Mercapto-l,2,4-thiadiazoles 3-Halo-l,2,4-thiadiazoles 3-Monoheteroarylamino thiadiazole 3-Phenyl triazolo thiadiazole 3.5- Disubstituted 1,2,4-thiadiazoles 4-Thiadiazole,2,5-bis 5- Amino-3-methyl-l,2,4-thiadiazole 5- Amino-l,2,3-thiadiazole 5- Chloro-1,2,4-thiadiazoles 5- Substituted 2-amino-l,3,4-thiadiazoles 5-Alkylamino-1,2,4-thiadiazole 5-Aryloxy-1,2,3-thiadiazoles 5-Chloro-l, 2, 3-thiadiazol 5-Dimethylamino-3-Phenyl 4-Thiadiazole 5-Ethoxy-3-trichloromethyl-1,2,4-thiadiazol 5-Methyl-l,3,4-thiadiazole-2-thiol 5-Unsubstituted 1,2,3-thiadiazoles 7- -3-(2-methyl-1,3,4-thiadiazol Alkoxy-1,3,4-thiadiazoles Alkylations 1,2,4-thiadiazole Amidines 1,2,4-thiadiazoles, 5-amino Amidinothioureas 1,2,4-thiadiazoles Amino-1,2,4-thiadiazoles chemistry Amino-1,2,4-thiadiazoles properties Amino-1,2,4-thiadiazoles synthesis Azoles Pyrazoles, Thiadiazoles, Thiazoles Benzimidazole thiadiazoles Benzo thiadiazole-1,1 -dioxide Benzo thiadiazoles Benzo-1,2,5-thiadiazole Benzo-2,l,3-thiadiazol Benzo-l,2,3-thiadiazole Benzo-l,2,3-thiadiazoles C2H2N2S 1,2,5-Thiadiazole Carboxy-1,3,4-thiadiazoles Chemistry (Cont of 1,3,4-thiadiazoles Chemistry of 1,3,4-thiadiazoles Chlorination 1.2.5- thiadiazole Condensed 1,2,4-Thiadiazoles Condensed Ring Systems incorporating 1,3,4-Thiadiazole Condensed Systems incorporating 4- Thiadiazoles Cycloaddition, 1,3-dipolar 1.2.3- thiadiazoles Diamino- 1,2,4-thiadiazoles Diamino- 1,2,4-thiadiazoles properties Diamino- 1,2,4-thiadiazoles synthesis Diazo-1,3,4-thiadiazoles Diazoamino-1,2,4-thiadiazoles Dimercapto-1,2,4-thiadiazole properties Dimethyl l,2,5-thiadiazole-3,4-dicarboxylate Dithiocarbazic 1,3,4-thiadiazoles Functionalizations 1,2,3-thiadiazole Fungicides 1,3,4-thiadiazoles Fused thiadiazoles Halogeno-1,3,4-thiadiazoles Halogeno-l,2,4-thiadiazoles Heterocycles 1,2,5-thiadiazole Heterocyclic compounds, aromatic thiadiazoles Heterocyclics thiadiazoles Hurd-Mori 1,2,3-thiadiazole synthesis Hurd-Mori synthesis of 1,2,3-thiadiazoles Hydrazino-1,3,4-thiadiazoles Hydrocarbons, hydrocarbon 1,2,5-thiadiazoles Hydroxy-l,2,5-thiadiazoles Imidazo -1,3,4-thiadiazoles Imidazo thiadiazole Imidazo thiadiazole bromination Imidazo thiadiazoles synthesis In the chemistry of 1,3,4-thiadiazoles Isothiocyanates 1.2.4- thiadiazoles, 5-amino Isoureas 1.2.4- thiadiazoles, 5-amino Isoxazoles forming 1,2,4-thiadiazoles Keto-1,3,4-thiadiazoles Kurzer 2 1,2,3-Thiadiazoles L,3,4-Thiadiazole-2,5-dione Mercapto-1,2,4-thiadiazoles Naphtho thiadiazoles Naphtho- -[ 1,2,5 thiadiazole Nitro-1,3,4-thiadiazoles Nitrosamino-1,2,4-thiadiazoles Of 1,3,4-thiadiazoles Oxadiazole, Oxazole, and Thiadiazole Polymers Oxadiazoles and Thiadiazoles Oxadiazoles or thiadiazoles Oxidative dimerization - 1,2,4-thiadiazole Phosgene 1.3.4- thiadiazol-2 -ones Photolysis of 1,2,3-thiadiazoles Polymeric 1,3,4-Thiadiazoles Polymers with pendant thiadiazole Properties of 1,2,3-Thiadiazoles Radicals from Oxadiazoles, Thiadiazoles, and Selenadiazoles Recent advances of 1,3,4-thiadiazoles Solid-Phase Synthesis of 1,2,4-Thiadiazoles Solid-Phase Synthesis of 1,3,4-Oxadiazoles and 1,3,4-Thiadiazoles via Selective Cyclization Spiro thiadiazoles Sulfonyl-1,3,4-thiadiazoles Synthesis of 1,2,4-Thiadiazoles Systems incorporating 1,2,5-Thiadiazole Thiadiazol-2-enes Thiadiazol-2-ones Thiadiazole C-Nucleosides Thiadiazole Derivatives for n-Type Semiconductors Thiadiazole aromaticity Thiadiazole chemical structures Thiadiazole crystal structures Thiadiazole derivatives Thiadiazole dioxides, decomposition Thiadiazole herbicides Thiadiazole polymers Thiadiazole structures Thiadiazole synthesis Thiadiazole, derivs Thiadiazole, electronic structure Thiadiazole-2-thiones Thiadiazole-fused heteroarenes Thiadiazoles 1,2,51 thiadiazolo pyrimidines Thiadiazoles 3-alkylthio— from Thiadiazoles Dimroth rearrangement Thiadiazoles and Selenathiadiazoles Thiadiazoles and Thiadiazolines Thiadiazoles and Triazoles Thiadiazoles and other 5-Membered Systems Thiadiazoles and selenadiazoles Thiadiazoles and selenodiazoles Thiadiazoles as Substrates Thiadiazoles decomposition Thiadiazoles electrochemical reduction Thiadiazoles formation Thiadiazoles quaternization Thiadiazoles radicals from Thiadiazoles reactions Thiadiazoles reactivity Thiadiazoles rearrangement Thiadiazoles thiol-thione tautomerism Thiadiazoles treatment Thiadiazoles, (continued Thiadiazoles, amino Thiadiazoles, amino-, tautomerism Thiadiazoles, computational studies Thiadiazoles, phosphorylated Thiadiazoles, photolysis Thiadiazoles, reduction Thiazole and thiadiazole 5-oxides Thiazole and thiadiazole S-oxides Thiazoles, and Thiadiazoles Thiazolo thiadiazoles Thiazolo-- and --thiadiazoles Thiazolo-l,3,4-thiadiazoles Thioketenes 1,2,3-thiadiazoles Thioketenes, from 1,2,3-thiadiazoles Thioketens from 1,2,3-Thiadiazoles Thiophene-1,3,4-thiadiazole Thiosemicarbazides 1.3.4- thiadiazoles Thiosemicarbazones 1.3.4- thiadiazoles Thiosemicarbazones 1.3.4- thiadiazoles, 2-amino Trichloromethylsulfenyl 1.2.4- thiadiazoles