MARC Record from marc_columbia

LEADER: 06256mam a2200349 a 4500
001 3301816
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008 020628t20022002flua b 001 0 eng d
020 $a0849310059
035 $a(OCoLC)ocm50082617
035 $9AUU0043CU
035 $a(NNC)3301816
035 $a3301816
040 $aCUS$cCUS$dNNC$dOrLoB-B
090 $aQD502.5$b.A45 2002
100 1 $aAhluwalia, V. K.$0http://id.loc.gov/authorities/names/nb99141252
245 10 $aOrganic reaction mechanisms /$cV.K. Ahluwalia, R.K. Parashar.
260 $aBoca Raton :$bCRC Press ;$aNew Delhi :$bNarosa Publishing House,$c[2002], ©2002.
300 $axx, 609 pages :$billustrations ;$c25 cm
336 $atext$btxt$2rdacontent
337 $aunmediated$bn$2rdamedia
504 $aIncludes bibliographical references and index.
505 00 $g1.$tChemical Kinetics and Reaction Pathways.$tChemical Kinetics, equilibria and energetics of reactions.$tNucleophilic substitution at saturated carbon atom.$tAddition reactions.$tElimination reactions.$tElectrophilic substitution in aromatic systems --$g2.$tReaction Intermediates, Ylides and Enamines.$tCarbocations.$tCarbanions.$tFree radicals.$tCarbenes.$tNitrenes.$tBenzynes.$tYlides.$tEnamines --$g3.$tOxidation.$tManganese (VII) oxidants.$tChromium (VI) oxidants.$tOxidation with peracids.$tMiscellaneous oxidants.$tEnzymatic or microbial oxidations (Bio-oxidations).$tCorrelation tables --$g4.$tReduction.$tHeterogeneous hydrogenation.$tHomogeneous hydrogenation.$tReduction with metal hydrides.$tReduction by dissolving metals.$tReduction by miscellaneous reducing agents.$tPhotoreduction.$tEnzymatic or microbial reductions (Bio-reductions).$tCorrelation tables --$g5.$tSome Reactions, Mechanisms and Applications.$tAcetoacetic ester synthesis.$tAldol condensation.$tAlgar-Flynn-Oyamada reaction.
505 80 $tArndt-Eistert synthesis.$tAuwers flavone synthesis.$tBaeyer-Villeger oxidation.$tBaker-Venktaraman rearrangement.$tBamford-Stevens reaction.$tBarbier-Wieland degradation.$tBarton reaction.$tBeckmann rearrangement.$tBenzidine rearrangement.$tBenzilic acid rearrangement.$tBenzoin condensation.$tBirch reduction.$tBouveault-Blanc reduction.$tCannizzaro reaction.$tChichibabin reaction.$tClaisen condensation.$tClaisen reaction.$tClaisen rearrangement.$tClaisen-Schmidt condensation.$tClemmensen reduction.$tCope elimination.$tCope rearrangement.$tDakin reaction.$tDarzens glycidic ester condensation.$tDieckmann condensation.$tDiels-Alder reaction.$tDebner-Miller synthesis.$tDuff reaction.$tEnamine reaction.$tEne reaction.$tElbs persulfate oxidation.$tEtard reaction.$tHaloform Reaction.$tHantzsch pyridine synthesis.$tHantzsch pyrrole synthesis.$tHell-Volhard-Zelinsky reaction.$tHenery reaction.$tHinsberg oxyindole synthesis.$tHinsberg thiophene synthesis.$tHofmann elimination.
505 80 $tHofmann isonitrile synthesis (Carbylamine reaction).$tHofmann-Martius rearrangement.$tHofmann rearrangement.$tHouben-Hoesh reaction.$tHunsdiecker reaction.$tJacobsen rearrangement.$tJones oxidation.$tKiliani-Fischer synthesis.$tKnoevenagel condensation.$tKnorr pyrazole synthesis.$tKnorr pyrrole synthesis.$tKnorr quinoline synthesis.$tKolbe electrolytic reaction.$tKolbe-Schmitt reaction.$tKostanecki-Robinson acylation.$tMadelung indole synthesis.$tMalonic ester synthesis.$tMannich reaction.$tMeerwein-Ponndorf-Verley reduction.$tMichael addition.$tMukaiyama reaction.$tNef reaction.$tNencki reaction.$tNorrish type cleavage.$tOppenauer oxidation.$tPaal-Knorr synthesis.$tPaterno-Buchi reaction.$tPechmann condensation.$tPerkin reaction.$tPinacol-pinacolone rearrangement.$tReformatsky reaction.$tReimer-Tiemann reaction.$tRitter reaction.$tRosenmund reduction.$tRosenmund-Von Braun synthesis.$tRuff-Fenton degradation.$tSabatier and Senderens reduction.$tSarett oxidation.
505 80 $tSchiemann reaction (Balz-Schimann reaction).$tSchotten-Baumann reaction.$tSimmons-Smith reaction.$tSkraup synthesis.$tStephen reaction.$tStobbe condensation.$tStrecker amino acid synthesis.$tSwern oxidation.$tThiele acetylation.$tThorpe (Ziegler) reaction.$tTischenko reaction.$tUllmann reaction.$tVilsmeier reaction (Vilsmeier-Haack reaction).$tWilliamson's ether synthesis.$tWohl-Ziegler reaction.$tWolff-Kishner reduction.$tWurtz reaction --$g6.$tMolecular Rearrangements.$tRearrangements involving migration to electron-deficient carbon.$tRearrangements involving migration to electron-deficient nitrogen.$tRearrangements involving migration to electron-deficient oxygen.$tRearrangements involving migration to electron-rich carbon.$tAromatic rearrangements --$g7.$tOrganometallic Compounds.$tGrignard reagents.$tOrganolithium compounds.$tOrganosilicon compounds.$tOrganocopper compounds.$tOrganozinc compounds.$tOrganoboranes.$tOrganocadmium compounds.$tOrganomercury compounds.$tOrganolead compounds.
505 80 $tOrganoaluminium compounds.$tOrganochromium compounds.$tOrganoiron compounds.$tOrganopalladium compounds.$tOrganorhodium and ruthenium compounds.$tOrganotellurium compounds --$g8.$tReagents.$tAluminium isopropoxide.$tN-Bromosuccinimide (NBS).$tDiazomethane.$t2, 3-Dichloro- 5, 6-dicyano-1, 4-benzoquinone (DDQ).$tN, N-Dicyclohexylcarbodiimide (DCC).$tLead tetra-acetate.$tLithium aluminium hydride.$tManganese dioxide.$tOrganoboranes.$tOrganosilicon compounds.$tOsmium tetroxide.$tSelenium dioxide.$tSodium borohydride.$tWittig reagent.
520 1 $a"This book, written explicitly for graduate and postgraduate students of chemistry, provides an extensive coverage of various organic reactions and rearrangements with emphasis on their application in synthesis. A summary of oxidation and reduction of organic compounds is given in tabular form (correlation tables) for the convenience of students. The most commonly encountered reaction intermediates are dealt with.
520 8 $aApplications of organic reagents illustrated with examples and problems at the end of each chapter will enable students to evaluate their understanding of the topic."--BOOK JACKET.
650 0 $aOrganic reaction mechanisms.$0http://id.loc.gov/authorities/subjects/sh98002135
700 1 $aParashar, R. K.$q(Rakesh Kumar)$0http://id.loc.gov/authorities/names/nb2001039419
852 00 $boff,che$hQD502.5$i.A45 2002g