LEADER 01312nam--2200397---450- 001 990000518670203316 005 20081203144246.0 010 $a88-464-2850-1 035 $a0051867 035 $aUSA010051867 035 $a(ALEPH)000051867USA01 035 $a0051867 100 $a20010620d2001----km-y0itay0103----ba 101 $aita 102 $aIT 105 $a||||||||001yy 200 1 $aInsegnare l'informatica in azienda$etecniche e metodologie per la formazione all'uso del compter nel mondo del lavoro$fMaurizio Duse 210 $aMilano$cF. Angeli$dcopyr. 2001 215 $a101 p.$d2 cm 225 2 $aFormazione permanente$v84 410 0$12001$aFormazione permanente 461 1$1001-------$12001 606 0 $aElaboratori elettronici$xImpiego nella formazione professionale 676 $a658.40380285 700 1$aDUSE,$bMaurizio$0382666 912 $a990000518670203316 951 $a658.403 DUS 1 (IRA 10 63)$b9338 E.C.$cIRA 10$d00073939 959 $aBK 969 $aECO 979 $aPAOLA$b40$c20010620$lUSA01$h1657 979 $aALESSANDRA$b40$c20010625$lUSA01$h1256 979 $c20020403$lUSA01$h1700 979 $aPATRY$b90$c20040406$lUSA01$h1636 979 $aRSIAV2$b90$c20081203$lUSA01$h1442 996 $aInsegnare l'informatica in azienda$9516637 997 $aUNISA LEADER 05174nam 2200649Ia 450 001 9910830429103321 005 20230721030834.0 010 $a1-281-37388-5 010 $a9786611373887 010 $a0-470-18116-8 010 $a0-470-18115-X 035 $a(CKB)1000000000403764 035 $a(EBL)343650 035 $a(SSID)ssj0000208012 035 $a(PQKBManifestationID)11175349 035 $a(PQKBTitleCode)TC0000208012 035 $a(PQKBWorkID)10240097 035 $a(PQKB)11379290 035 $a(MiAaPQ)EBC343650 035 $a(OCoLC)664606186 035 $a(EXLCZ)991000000000403764 100 $a20070813d2008 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 14$aThe naphthyridines$b[electronic resource] /$fD.J. Brown 210 $aHoboken, N.J. $cWiley$dc2008 215 $a1 online resource (448 p.) 225 1 $aThe chemistry of heterocyclic compounds ;$v63 300 $a"An Interscience publication." 311 $a0-471-75159-6 320 $aIncludes bibliographical references (p. 295-336) and index. 327 $aTHE NAPHTHYRIDINES; Contents; CHAPTER 1 PRIMARY SYNTHESES OF 1,5-NAPHTHYRIDINES; 1.1 From a Single Aliphatic Substrate; 1.2 From a Single Pyridine Substrate; 1.2.1 By Formation of the N1,C2-Bond; 1.2.2 By Formation of the C3,C4-Bond; 1.2.3 By Formation of the C4,C4a-Bond; 1.3 From a Pyridine Substrate with One Synthon; 1.3.1 Where the Synthon Supplies One Atom; 1.3.2 Where the Synthon Supplies Two Atoms; 1.3.3 Where the Synthon Supplies Three Atoms; 1.4 From a Pyridine Substrate and Two Synthons; 1.5 From Other Heterocyclic Substrates 327 $aCHAPTER 2 1,5-NAPHTHYRIDINE, ALKYL-1,5- NAPHTHYRIDINES, AND ARYL-1,5- NAPHTHYRIDINES2.1 1,5-Naphthyridine; 2.1.1 Preparation of 1,5-Naphthyridine; 2.1.2 Properties of 1,5-Naphthyridine; 2.1.3 Reactions of 1,5-Naphthyridine; 2.2 Alkyl- and Aryl-1,5-Naphthyridines; 2.2.1 Preparation of Alkyl- and Aryl-1,5-Naphthyridines; 2.2.2 Reactions of Alkyl- and Aryl-1,5-Naphthyridines; CHAPTER 3 HALOGENO-1,5-NAPHTHYRIDINES; 3.1 Preparation of Halogeno-1,5-Naphthyridines; 3.1.1 By Direct Halogenation; 3.1.2 By Halogenolysis of 1,5-Naphthyridinones or the Like 327 $a3.1.3 By the Meissenheimer Reaction on 1,5-Naphthyridine N-Oxides3.1.4 By Miscellaneous Procedures; 3.2 Reactions of Halogeno-1,5-Naphthyridines; 3.2.1 Alcoholysis or Phenolysis of Halogeno-1, 5-Naphthyridines; 3.2.2 Aminolysis of Halogeno-1,5-Naphthyridines; 3.2.3 Other Reactions of Halogeno-1,5-Naphthyridines; CHAPTER 4 OXY-1,5-NAPHTHYRIDINES; 4.1 Tautomeric 1,5-Naphthyridinones and Extranuclear Hydroxy-1,5-Naphthyridines; 4.1.1 Preparation of Tautomeric 1,5-Naphthyridinones and the Like; 4.1.2 Reactions of Tautomeric 1,5-Naphthyridinones and the Like 327 $a4.2 Alkoxy- and Aryloxy-1,5-Naphthyridines4.3 Nontautomeric 1,5-Naphthyridinones; 4.4 1,5-Naphthyridine N-Oxides; CHAPTER 5 THIO-1,5-NAPHTHYRIDINES; CHAPTER 6 NITRO-, AMINO-, AND RELATED 1,5-NAPHTHYRIDINES; 6.1 Nitro-1,5-Naphthyridines; 6.1.1 Preparation of Nitro-1,5-Naphthyridines; 6.1.2 Reactions of Nitro-1,5-Naphthyridines; 6.2 Amino- and (Substituted-Amino)-1,5-Naphthyridines; 6.2.1 Preparation of Amino-1,5-Naphthyridines; 6.2.2 Reactions of Amino-1,5-Naphthyridines; CHAPTER 7 1,5-NAPHTHYRIDINECARBOXYLIC ACIDS AND RELATED DERIVATIVES; 7.1 1,5-Naphthyridinecarboxylic Acids 327 $a7.2 1,5-Naphthyridinecarboxylic Esters7.3 1,5-Naphthyridinecarboxamides, Carbonitriles, Carbaldehydes, and Ketones; CHAPTER 8 PRIMARY SYNTHESES OF 1,6-NAPHTHYRIDINES; 8.1 By Condensation of Two or More Aliphatic Substrates/Synthons; 8.2 From a Single Pyridine Substrate; 8.3 From a Pyridine Substrate with One Synthon; 8.3.1 Where the Synthon Supplies One Ring Atom; 8.3.2 Where the Synthon Supplies Two Ring Atoms; 8.3.3 Where the Synthon Supplies Three or More Ring Atoms; 8.4 From a Pyridine Substrate with Two or More Synthons; 8.5 From Other Heterocyclic Systems 327 $aCHAPTER 9 1,6-NAPHTHYRIDINE, ALKYL-1,6- NAPHTHYRIDINES, AND ARYL-1,6- NAPHTHYRIDINES 330 $aA volume in the Chemistry of Heterocyclic Compounds series, this book provides a summary of the chemistry of each of the six naphthyridine systems along with tables of known simple derivatives with original references.Each of the six naphthyridine systems are described in valuable detail and coverage includes: Primary synthetic methods from non-naphthyridine substrates; Chemistry and properties of the parent heterocycle and its simple alkyl derivatives; Formation and reactions of halogeno derivatives; formation and reactions of hydroxy, oxo, alkoxy, and related derivatives. 410 0$aChemistry of heterocyclic compounds. 606 $aPyridine$xDerivatives 606 $aChemistry 615 0$aPyridine$xDerivatives. 615 0$aChemistry. 676 $a547.59 676 $a547/.59/05 676 $a547/.593 700 $aBrown$b D. J$0383088 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830429103321 996 $aThe naphthyridines$93995393 997 $aUNINA