LEADER 00931nam a22002651i 4500 001 991003816079707536 005 20030922114422.0 008 031111s1989 uika||||||||||||||||eng 020 $a0713631341 035 $ab12477655-39ule_inst 035 $aARCHE-051093$9ExL 040 $aDip.to Lingue$bita$cA.t.i. Arché s.c.r.l. Pandora Sicilia s.r.l. 082 04$a822.808 245 00$aVictorian theatre /$cedited by Russel Jackson 260 $aLondon :$bA & Black,$c1989 300 $a370 p. :$bill. ;$c20 cm 440 4$aThe new mermaids 650 4$aTeatro inglese$ySec. 19.$xCritica 700 1 $aJackson, Russell 907 $a.b12477655$b02-04-14$c13-11-03 912 $a991003816079707536 945 $aLE012 822.808 JAC$g1$i2012000153257$lle012$o-$pE0.00$q-$rl$s- $t0$u1$v0$w1$x0$y.i12909634$z13-11-03 996 $aVictorian theatre$9180894 997 $aUNISALENTO 998 $ale012$b13-11-03$cm$da $e-$feng$guik$h0$i1 LEADER 05250nam 2200709Ia 450 001 9911019215403321 005 20200520144314.0 010 $a9786612301377 010 $a9781282301375 010 $a1282301373 010 $a9780470186527 010 $a0470186526 010 $a9780470188026 010 $a0470188022 035 $a(CKB)1000000000376511 035 $a(EBL)469493 035 $a(OCoLC)814414783 035 $a(SSID)ssj0000366732 035 $a(PQKBManifestationID)11283102 035 $a(PQKBTitleCode)TC0000366732 035 $a(PQKBWorkID)10418680 035 $a(PQKB)10532332 035 $a(MiAaPQ)EBC469493 035 $a(PPN)221766618 035 $a(Perlego)2786674 035 $a(EXLCZ)991000000000376511 100 $a19840717d1952 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aThiophene and its derivatives /$fHoward D. Hartough 205 $a99th ed. 210 $aNew York $cWiley$d1952 215 $a1 online resource (554 p.) 225 1 $aThe chemistry of heterocyclic compounds ;$v3 300 $aDescription based upon print version of record. 311 08$a9780470375549 311 08$a047037554X 320 $aIncludes bibliographies and indexes. 327 $aThiophene and Its Derivatives; Preface; Contents; I. General Discussion; I. History of Thiophene; II. Nomenclature of Thiophene Compounds; III. Occurrence of Thiophene Compounds in Nature; IV. Color Reactions of Thiophene Compounds; V. Estimation of Thiophene; VI. Removal of Thiophene and Its Homologs from Coal Tar Aromatics and Petroleum Stocks; VII. Isomorphism and Physical Properties of Thiophene Compounds; VIII. Odor of Thiophene and Its Derivatives; II. Biological and Pharmacological Activity of Thiophene and Its Derivatives; Introduction; I. General Biological Effects 327 $aII. Antihistamine CompoundsIII. Pressor Compounds; IV. Local Anesthetics; V. Hypnotics; VI. Antifebrides and Analgesics; VII. Antispasmodics; VIII. Anticonvulsants; IX. Germicides; X. Analogs of DDT; XI. Miscellaneous Compounds and Their Properties; III. Synthesis and Physical Properties of Thiophene and Its Homologs; I. Synthesis of Thiophene and Its Homologs; A. Synthesis of Thiophene and Its Homologs by Ring Closure of Hydrocarbons; 1. Socony-Vacuum Thiophene Process; (a) The Process; (b) Flow of Materials; (c) Equipment; 2. Miscellaneous Methods 327 $aB. Ring Closure of ?-Diketones, ?-Diacides, or ?-Keto AcidsII. Physical Properties of Thiophene and Its Homologs; III. Synthesis and Properties of the Hydrothiophenes; A. Thioplenes (Dihydrothiophenes); B. Dihydrothianaphthenes; C. Thiolanes; D. Preparation of 3-Thiolene- and Thiolanecarboxylic Acids; IV. Moloecular Structure and Spectroscopy of the Thiophene and Its Derivatives; Introduction; I. Molecular Structure and Related Properties; A . Bond Distances and Angles of Thiophene; B. Dipole Moments and Resonance in Thiophene Nucleus; C. Miscellanceous Related Properties 327 $aII. Theoretical Considerations from the Viewpoint of Spectroscopy and Summary of Published Spectral DataA. Electronic Absorption Spectra; B. Electronic Emission Spectra; C. Vibration Spectra; D. Thermodynamic Functions from Spectroscopic and Molecular Structure Data; III. Applied Spectroscopy; Introduction; A. Ultraviolet Absorption Spectra; B. Infrared Absorption Spectra; C. Mass Spectral Data; V. Factors Affecting Substitution Reactions in the Thiophene Nucleus; Introduction; I . Resonance in the Thiophene Nucleus; II. Directive Influcncc of the Sulfur Atom in Monosubstitution Reactions 327 $aIII. Directive Influences of Typical Ortho-para-Directing Groups on the Thiophene NucleusIV. Directive Influences of Typical Meta-Directing Groups; V. Methods of Synthesis in the Thiophene Series Based on Directive Influences in the Thiophene Nucleus; A. Preparation of 3-Substituted Thiophenes; 3-Alkylthiophenes; 3-Nitrothiophene; 3-Chlorothiophene; 3-Bromothiophene; 3-Iodothiophene; 3,4-Diaminothiophene; 3-Thenyl Bromide and Some of Its Reactions; B. Syntheses Involving the 3-Methylthiophene Nucleus; C. Synthesis of the Six Isomeric Methylthiophenecarboxylic Acids 327 $a5-Methyl-2-thiophenecarboxylic Acid (I) 330 $aChemistry of Heterocyclic Compounds publishes articles, letters to the Editor, reviews, and minireviews on the synthesis, structure, reactivity, and biological activity of heterocyclic compounds including natural products. The journal covers investigations in heterocyclic chemistry taking place in scientific centers of all over the world, including extensively the scientific institutions in Russia, Ukraine, Latvia, Lithuania and Belarus. 410 0$aChemistry of heterocyclic compounds ;$v3. 606 $aThiophenes 606 $aHeterocyclic compounds 615 0$aThiophenes. 615 0$aHeterocyclic compounds. 676 $a547.594 700 $aHartough$b H. D$g(Howard Dale),$f1913-1992.$0947072 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9911019215403321 996 $aThiophene and its derivatives$94417870 997 $aUNINA