LEADER 01936oam 2200493zu 450 001 996201368803316 005 20210807003446.0 035 $a(CKB)111055184226314 035 $a(SSID)ssj0000396134 035 $a(PQKBManifestationID)12128387 035 $a(PQKBTitleCode)TC0000396134 035 $a(PQKBWorkID)10461284 035 $a(PQKB)10964225 035 $a(EXLCZ)99111055184226314 100 $a20160829d2001 uy 101 0 $aeng 181 $ctxt 182 $cc 183 $acr 200 10$aAPSEC 2001 : Eighth Asia-Pacific Software Engineering Conference : proceedings : 4-7 December, 2001, Macao, China 210 31$a[Place of publication not identified]$cIEEE Computer Society Press$d2001 300 $aBibliographic Level Mode of Issuance: Monograph 311 $a0-7695-1408-1 606 $aSoftware engineering$xDevelopment$vCongresses 606 $aObject-oriented programming (Computer science)$vCongresses 606 $aComputer software$vCongresses 606 $aEngineering & Applied Sciences$2HILCC 606 $aComputer Science$2HILCC 615 0$aSoftware engineering$xDevelopment 615 0$aObject-oriented programming (Computer science) 615 0$aComputer software 615 7$aEngineering & Applied Sciences 615 7$aComputer Science 676 $a005.1/17 712 02$aAomen da xue 712 02$aInternational Institute for Software Technology 712 02$aMacau (China : Special Administrative Region) Gabinete para o Desenvolvimento das Telecomunicações e Tecnologias da Informação. 712 02$aGuo jia zi ran ke xue ji jin wei yuan hui (China) 712 12$aAsia-Pacific Software Engineering Conference 801 0$bPQKB 906 $aPROCEEDING 912 $a996201368803316 996 $aAPSEC 2001 : Eighth Asia-Pacific Software Engineering Conference : proceedings : 4-7 December, 2001, Macao, China$92379489 997 $aUNISA LEADER 05041nam 2200697 a 450 001 9911020229203321 005 20200520144314.0 010 $a9786610542000 010 $a9781280542008 010 $a1280542004 010 $a9780471656999 010 $a0471656992 010 $a9780471656913 010 $a0471656917 035 $a(CKB)111090529064314 035 $a(EBL)183816 035 $a(SSID)ssj0000120566 035 $a(PQKBManifestationID)11146493 035 $a(PQKBTitleCode)TC0000120566 035 $a(PQKBWorkID)10081055 035 $a(PQKB)10996486 035 $a(MiAaPQ)EBC183816 035 $a(OCoLC)85820589 035 $a(Perlego)2783781 035 $a(EXLCZ)99111090529064314 100 $a20040610d2004 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 14$aThe chemistry of 1,2,3-Thiadiazoles /$fVasiliy A. Bakulev, Wim Dehaen 210 $aHoboken, N.J. $cJohn Wiley & Sons$dc2004 215 $a1 online resource (261 p.) 225 1 $aThe chemistry of heterocyclic compounds ;$vv. 62 300 $aDescription based upon print version of record. 311 08$a9780471326625 311 08$a0471326623 320 $aIncludes bibliographical references and index. 327 $aTHE CHEMISTRY OF 1,2,3-THIADIAZOLES; The Chemistry of Heterocyclic Compounds Introduction to the Series; Preface; Acknowledgments; Contents; 1 Synthesis of 1,2,3-thiadiazoles; 1.1 Cyclization of Hydrazones with Thionyl Chloride (Hurd-Mori Synthesis); 1.1.1 Scope and Limitations; 1.1.2 Mechanism of the Hurd-Mori Reaction; 1.1.3 Application of the Hurd-Mori Reaction in Organic Synthesis; 1.2 Cycloaddition of Diazoalkanes onto a C=S bond (Pechmann Synthesis); 1.3 Heterocyclization of ?-diazo Thiocarbonyl Compounds (Wolff Synthesis) 327 $a1.3.1 Introduction of a Diazo Function into Compounds Containing a C=S Bond1.3.2 Introduction of a C=S Bond in the ?-position to a Diazo Group; 1.3.3 Simultaneous Introduction of Diazo and Thiocarbonyl Functions; 1.4 Transformations of other Sulfur-containing Heterocyclic Compounds; 1.5 Elaboration of Preformed 1,2,3-Thiadiazoles; 1.5.1 Carboxylic Acids; 1.5.2 Functional Derivatives of Carboxylic Acids; 1.5.3 Aldehydes; 1.5.4 Amino-1,2,3-Thiadiazoles; 1.5.5 Halo Derivatives; 1.5.6 5-Hydrazino-, 5-Mercapto-1,2,3-Thiadiazoles and 5-Sulfide Derivatives 327 $a1.5.7 2-(1,2,3-Thiadiazol-5-yl)acetic Acid Derivatives1.5.8 Alkenyl-1,2,3-Thiadiazoles; 1.5.9 5-Hydroxyiminomethyl- and 5-Diazomethyl-1,2,3-Thiadiazoles; 1.5.10 4-Hydroxymethyl-1,2,3-Thiadiazoles; 1.6 Tables; 1.7 Selected Procedures; 1.7.1 1,2,3-Thiadiazole-4-Carbaldehyde; 1.7.2 4-Phenyl-1,2,3-Thiadiazole; 1.7.3 4-Phenyl-1,2,3-Thiadiazole-5-Carbaldehyde; 1.7.4 4-Phenyl-5-Oxyiminomethyl-1,2,3-Thiadiazole; 1.7.5 5-Phenyl-1,2,3-Thiadiazole-4-Carbaldehyde; 1.7.6 5-Chloro-1,2,3-Thiadiazole-4-Carbaldehyde; 1.7.7 Ethyl 5-amino-1,2,3-Thiadiazole-4-Carboxylate; 1.7.7.1 Pechmann Method 327 $a1.7.7.2 Wolff Method1.7.8 Ethyl 5-chloro-1,2,3-Thiadiazole-4-Carboxylate; 1.7.9 4-Phenyl-2-(2,4,6-Trichlorophenyl)-1,2,3-Thiadiazolium Chloride; 1.7.10 5-Amino-4-ethoxycarbonyl-2-phenyl-1,2,3-thiadiazolium bromide; References; 2 Structure of 1,2,3-Thiadiazoles; 2.1 Theoretical Methods; 2.2 Experimental Structural Methods; 2.2.1 X-ray Analysis; 2.2.2 Nuclear Magnetic Resonance Spectroscopy; 2.2.2.1 Proton NMR Spectroscopy; 2.2.2.2 Carbon-13 NMR Spectroscopy; 2.2.2.3 Nitrogen-14 NMR Spectroscopy; 2.2.2.4 Nitrogen-15 NMR Spectroscopy; 2.2.3 Mass Spectrometry; 2.2.4 Other Spectroscopic Data 327 $aReferences3 Chemical Properties of 1,2,3-Thiadiazoles; 3.1 Reactions due to the Reactivity of Ring Atoms; 3.1.1 Reactions with Electrophiles; 3.1.1.1 Protonation; 3.1.1.2 Complexation; 3.1.1.3 Alkylation; 3.1.1.4 Acylation; 3.1.1.5 Oxidation; 3.1.1.6 Electrophilic Substitution of Hydrogen; 3.1.2 Reactions with Nucleophiles; 3.1.2.1 Attack at the Sulfur Atom; 3.1.2.2 Attack at the C(5) Atom; 3.1.2.3 Attacks at H(4) and H(5); 3.1.2.4 Cycloaddition Reactions; 3.2 Reactions of Substituents; 3.2.1 5-Alkyl-1,2,3-thiadiazoles; 3.2.2 1,2,3-Thiadiazole-4-carbaldehyde 327 $a3.2.3 5-Amino-1,2,3-thiadiazole-4-carbothioamide 330 $a1,2,3-Thiadiazoles are a group of heterocycles whose derivatives are important in industry, medicine, and agriculture. This volume provides a complete treatment of this group of heterocycles with an emphasis on syntheses, structural data, properties, reactions, and applications. 410 0$aChemistry of heterocyclic compounds ;$vv. 62. 606 $aThiadiazoles 615 0$aThiadiazoles. 676 $a547.59 676 $a547.594 676 $a547/.59/05 700 $aBakulev$b Vasiliy A$01838928 701 $aDehaen$b W$g(Wim)$01838929 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9911020229203321 996 $aThe chemistry of 1,2,3-Thiadiazoles$94418022 997 $aUNINA