命名反应
2008-3
科学出版社
Jie Jack Li
652
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本书第三版相对前两版有了显著改进，主题索引显著扩大。为了更新参考文献，每个反应现在均补充了2—3个展现其合成能力的典型合成实例。本书与其他的命名反应类图书不同，重点介绍反应的有机化学机理。它涵盖300多个经典以及当代的命名反应。每一个反应都给出其详细的步骤，电子转移机理，辅以原有的和最新的参考资料。 本书可供有机化学、药物化学和生物化学等专业高年级本科生、研究生以及科研人员参考。
作者：(美国)李(Jie Jack Li)
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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机理很详细，有助于有机化学反应的学习
这本书就是华中理工大学容国斌翻译的《有机人名反应与机理》的原版，不过容国斌翻译的是第二版，这是最新的第三版，比起第二版来多了不少例子！
反应机理写的很详细
国外经典著作
很经典，内容全，装帧好，价格适中，做为字典一样的参考书再好不过了。
书质量不错 但皮有点花
书本不错，比较全面的
书籍的角有破损。其他还好。
书不错，质量靠得住
封皮都磕碎了。书不错
速度快，书也不错，没有明显旧痕
除了送货慢了一点其他目前都好。
全英文版本，书的质量还好
适合科研和学习用 全面
内容不错，与人名反应配套使用很好！但是，书中有些错误，不知是印刷错误还是怎么的。印刷比较差，纸张很差，装订很差！
有机化学领域的最经典书之一
书看起来挺不错，印刷和纸张质量都挺好
怎么说那这本书是第三版了,之前荣国斌翻译的是第二版.有时侯听到一个不熟悉的人名反应,就会查阅这本书,此外比第二版多了示例.买了这本书,再买一本英文的命名反应在有机合成中的应用策略,可以说人名反应就没有不知道的了