命名反應(yīng)

內(nèi)容概要

本書第三版相對前兩版有了顯著改進，主題索引顯著擴大。為了更新參考文獻，每個反應(yīng)現(xiàn)在均補充了2—3個展現(xiàn)其合成能力的典型合成實例。本書與其他的命名反應(yīng)類圖書不同，重點介紹反應(yīng)的有機化學(xué)機理。它涵蓋300多個經(jīng)典以及當(dāng)代的命名反應(yīng)。每一個反應(yīng)都給出其詳細的步驟，電子轉(zhuǎn)移機理，輔以原有的和最新的參考資料。    本書可供有機化學(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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