出版時(shí)間:2008-3 出版社:科學(xué)出版社 作者:Jie Jack Li 頁數(shù):652
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內(nèi)容概要
本書第三版相對前兩版有了顯著改進(jìn),主題索引顯著擴(kuò)大。為了更新參考文獻(xiàn),每個(gè)反應(yīng)現(xiàn)在均補(bǔ)充了2—3個(gè)展現(xiàn)其合成能力的典型合成實(shí)例。本書與其他的命名反應(yīng)類圖書不同,重點(diǎn)介紹反應(yīng)的有機(jī)化學(xué)機(jī)理。它涵蓋300多個(gè)經(jīng)典以及當(dāng)代的命名反應(yīng)。每一個(gè)反應(yīng)都給出其詳細(xì)的步驟,電子轉(zhuǎn)移機(jī)理,輔以原有的和最新的參考資料。 本書可供有機(jī)化學(xué)、藥物化學(xué)和生物化學(xué)等專業(yè)高年級本科生、研究生以及科研人員參考。
作者簡介
作者:(美國)李(Jie Jack Li)
書籍目錄
AbbreviationsAlder ene reactionAldol condensationAlgar-Flynn-Oyamada reactionAllan-Robinson reactionAppel reactionArndt-Eistert homologationBaeyer-Villiger oxidationBaker-Venkataraman rearrangementBamberger rearrangementBamford-Stevens reactionBarbier coupling reactionBargellini reactionBartoli indole synthesisBarton radical decarboxylationBarton-McCombie deoxygenationBarton nitrite photolysisBarton-Zard reactionBatcho-Leimgruber indole synthesisBaylis-Hillman reactionBeckmann rearrangementBeirut reactionBenzilic acid rearrangementBenzoin condensationBergman cyclization.Biginelli pyrimidone synthesisBirch reductionBischler-Mthlau indole synthesisBischler-Napieralski reactionBlaise reactionBlanc chloromethylationBlum aziridine synthesisBoekelheide reactionBoger pyridine synthesisBorch reductive aminationBorsche-Drechsel cyclizationBoulton-Katritzky rearrangementBouveault aldehyde synthesisBouveault-Blanc reductionBoyland-Sims oxidationBradsher reactionBrook rearrangementBrown hydroborationBucherer carbazole synthesisBucherer reactionBucherer-Bergs reactionBuchner-Curtius-Schlotterbeck reactionBuchner method of ring expansionBuchwald-Hartwig C-N bond and C-O bond formation reactionsBurgess dehydrating reagentCadiot--Chodkiewicz couplingCamps quinolinol synthesisCannizzaro dispropotionationCarroll rearrangementCastro-Stephens couplingChan alkyne reductionChan-Lam coupling reactionChapman rearrangementChichibabin pyridine synthesisChugaev reactionCiamician-Dennsted rearrangementClaisen condensationClaisen isoxazole synthesisClaisen rearrangementAbnormal Claisen rearrangementEschenmoser-Claisen amide acetal rearrangementIreland--Claisen (silyl ketene acetal) rearrangementJohnson-Claisen (orthoester) rearrangementClemmensen reductionCombes quinoline synthesisConrad-Limpach reactionCope elimination reactionCope rearrangementOxy-Cope rearrangementAnionic oxy-Cope rearrangementCorey-Bakshi-Shibata (CBS) reductionCorey--Chaykovsky reactionCorey-Fuchs reactionCorey-Kim oxidationCorey-Nicolaou macrolactonizationCorey-Seebach dithiane reactionCorey-Winter olefin synthesisCriegee glycol cleavageCriegee mechanism of ozonolysisCurtius rearrangementDakin oxidationDakin-West reactionDanheiser annulation Darzens glycidic ester condensationDavis chiral oxaziridine reagentDelepine amine synthesisde Mayo reactionDemjanov rearrangementTiffeneau-Demjanov rearrangement Dess-Martin oxidation Dieckmann condensationDiels-Alder reaction Dienone-phenol rearrangementDi-π-methane rearrangement Doebner quinoline synthesis Dptz reactionDowd-Beckwith ring expansionEdenmeyer-Plochl azlactone synthesisEschenmoser-Tanabe fragmentationEschweiler-Clarke reductive alkylation of aminesEvans aldol reactionFavorskii rearrangement and quasi-Favorskii rearrangementFeist-Benary furan synthesisFerrier carbocyclizationFerrier glycal allylic rearrangementFiesselmann thiophene synthesisFischer indole synthesisFischer oxazole synthesisFleming-Tamao oxidationTamao-Kumada oxidationFriedel-Crafts reactionFriedlander quinoline synthesis Fries rearrangementFukuyama amine synthesisFukuyama reduction Gabriel synthesisIng-Manske procedureGabriel-Colman rearrangementGassman indole synthesisGattermann-Koch reactionGewald aminothiophene synthesisGlaser coupling Eglinton couplingGomberg-Bachmann reactionGould-Jacobs reactionGrignard reactionGrob fragmentationGuareschi-Thorpe condensationHajos-Wiechert reactionHailer-Bauer reactionHantzsch dihydropyridine synthesisHantzsch pyrrole synthesisHeck reactionHeteroaryl Heck reactionHegedus indole synthesisHell-Volhard-Zelinsky reactionHenry nitroaldol reactionHinsberg synthesis of thiophene derivativesHiyama cross-coupling reactionHiyama-Denmark cross-coupling reactionHofmann rearrangementHofmann-Loffler-Freytag reactionHorner-Wadsworth-Emmons reactionHouben-Hoesch synthesisHunsdiecker-Borodin reactionHurd-Mori 1,2,3-thiadiazole synthesisJacobsen-Katsuki epoxidationJapp--Klingemann hydrazone synthesisJones oxidationJulia-Kocienski olefinationJulia-Lythgoe olefinationKahne--Crich glycosidationKeck macrolactonizationKnoevenagel condensationKnorr pyrazole synthesisPaal-Knorr pyrrole synthesisKoch-Haaf carbonylationKoenig-Knorr glycosidationKolbe-Schmitt reactionKostanecki reactionKrohnke pyridine synthesisKumada cross-coupling reactionLawesson's reagentLeuckart-Wallach reaction Lossen rearrangementMcFadyen-Stevens reductionMcMurry couplingMacMillan catalystMannich reactionMarshall boronate fragmentationMartin's sulfurane dehydrating reagentMasamune-Roush conditionsMeerwein-Ponndorf-Verley reductionMeisenheimer complex[1,2]-Meisenheimer rearrangement[2,3]-Meisenheimer rearrangementMeth-Cohn quinoline synthesis Meyers oxazoline methodMeyer-Schuster rearrangementMichael additionMichaelis-Arbuzov phosphonate syathesisMidland reductionMislow-Evans rearrangementMitsunobu reactionMiyaura borylation Moffatt oxidation Montgomery coupling Morgan-Walls reactionPictet-Hubert reaction Moil-Ban indole synthesis Mukaiyama aldol reaction Mukaiyama Michael addition Mukaiyama reagent Myers-Saito cyclization Nazarov cyclization Neber rearrangement Nef reaction Negishi cross-coupling reactionNenitzescu indole synthesis Nicholas reaction Nicolaou dehydrogenation Nicolaou hydroxy-dithioketal cyelizationNicolaou hydroxy-ketone reductionNicolaou oxyselenation Noyori asymmetric hydrogenationNozaki-Hiyama-Kishi reactionOppenauer oxidation Overman rearrangement Paal thiophene synthesis Paal-Knorr furan synthesis Parham cyclization Passerini reaction Patemt-Buchi reaction Pauson-Khand cyclopentenone synthesisPayne rearrangement Pechmann coumarin synthesisPerkin reactionPetasis reactionPeterson olefination Pictet--Gams isoquinoline synthesisPictet-Spengler tetrahydroisoquinoliPinacol rearrangement Pinner reactionPolonovski reactionPolonovski-Potier rearrangementPomeranz-Fritsch reactionSchlittler-M011er modificationPrevost trans-dihydroxylationWoodward cis-dihydroxylationPrins reactionPschorr cyclizationPummerer rearrangementRamberg-Baicklund reactionReformatsky reactionRegitz diazo synthesisReimer-Tiemann reactionReissert aldehyde synthesisReissert indole synthesisRing-closing metathesisRitter reactionRobinson annulationRobinson-Gabriel synthesisRobinson-Schopf reactionRosenmund reductionRubottom oxidationRupe rearrangementSaegusa oxidationSakurai allylation reactionSandmeyer reactionSchiemann reactionSchmidt reactionSchmidt's trichloroacetimidate glycosidation reactionShapiro reactionSharpless asymmetric amino hydroxylationSharpless asymmetric epoxidationSharpless asymmetric dihydroxylationSharpless olefin synthesisSimmons-Smith reaction Skraup quinoline synthesisDoebner-von Miller reactionSmiles rearrangementNewman-Kwart reactionTruce-Smile rearrangementSommelet reactionSommelet-Hauser rearrangementSonogashira reactionStaudinger ketene cycloadditionStaudinger reductionStembach benzodiazepine synthesisStetter reactionStill-Gennari phosphonate reactionStille couplingStille-Kelly reactionStobbe condensationStork enamine reactionStrecker amino acid synthesis Suzuki coupling.Swem oxidation Takai iodoalkene synthesisTebbe olefinationPetasis alkenylationTEMPO-mediated oxidationThorpe-Ziegler reactionTsuji-Trost allylationUgi reactionUllmann reactionvan Leusen oxazole synthesisVilsmeier-Haack reactionVilsmeier mechanism for acid chloride formationVinylcyclopropane-cyclopentene rearrangementvon Braun reactionWacker oxidationWagner-Meerwein rearrangementWeiss-Cook reactionWharton oxygen transposition reactionWillgerodt-Kindler reactionWittig reactionSchlosser modification of the Wittig reaction[ 1,2]-Wittig rearrangement[2,3]-Wittig rearrangementWohl-Ziegler reactionWolff rearrangementWolff-Kishner reductionYamaguchi esterificationZincke reactionSubject Index
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