命名反應(yīng)：詳細(xì)反應(yīng)機(jī)理大全（第三版）

定　價(jià)：￥98.00

作　者：	（美國(guó)）（Jie Jack Li）李
出版社：	科學(xué)出版社
叢編項(xiàng)：	國(guó)外化學(xué)名著系列
標(biāo)　簽：	有機(jī)化學(xué)

購(gòu)買(mǎi)這本書(shū)可以去

ISBN：	9787030211910	出版時(shí)間：	2008-03-01	包裝：	平裝
開(kāi)本：	16	頁(yè)數(shù)：	652 pages	字?jǐn)?shù)：

內(nèi)容簡(jiǎn)介

　　本書(shū)第三版相對(duì)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(shū)與其他的命名反應(yīng)類圖書(shū)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(shū)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(jí)本科生、研究生以及科研人員參考。

作者簡(jiǎn)介

暫缺《命名反應(yīng)：詳細(xì)反應(yīng)機(jī)理大全（第三版）》作者簡(jiǎn)介

圖書(shū)目錄

Abbreviations
Alder ene reaction
Aldol condensation
Algar-Flynn-Oyamada reaction
Allan-Robinson reaction
Appel reaction
Arndt-Eistert homologation
Baeyer-Villiger oxidation
Baker-Venkataraman rearrangement
Bamberger rearrangement
Bamford-Stevens reaction
Barbier coupling reaction
Bargellini reaction
Bartoli indole synthesis
Barton radical decarboxylation
Barton-McCombie deoxygenation
Barton nitrite photolysis
Barton-Zard reaction
Batcho-Leimgruber indole synthesis
Baylis-Hillman reaction
Beckmann rearrangement
Beirut reaction
Benzilic acid rearrangement
Benzoin condensation
Bergman cyclization.
Biginelli pyrimidone synthesis
Birch reduction
Bischler-Mthlau indole synthesis
Bischler-Napieralski reaction
Blaise reaction
Blanc chloromethylation
Blum aziridine synthesis
Boekelheide reaction
Boger pyridine synthesis
Borch reductive amination
Borsche-Drechsel cyclization
Boulton-Katritzky rearrangement
Bouveault aldehyde synthesis
Bouveault-Blanc reduction
Boyland-Sims oxidation
Bradsher reaction
Brook rearrangement
Brown hydroboration
Bucherer carbazole synthesis
Bucherer reaction
Bucherer-Bergs reaction
Buchner-Curtius-Schlotterbeck reaction
Buchner method of ring expansion
Buchwald-Hartwig C-N bond and C-O bond formation reactions
Burgess dehydrating reagent
Cadiot--Chodkiewicz coupling
Camps quinolinol synthesis
Cannizzaro dispropotionation
Carroll rearrangement
Castro-Stephens coupling
Chan alkyne reduction
Chan-Lam coupling reaction
Chapman rearrangement
Chichibabin pyridine synthesis
Chugaev reaction
Ciamician-Dennsted rearrangement
Claisen condensation
Claisen isoxazole synthesis
Claisen rearrangement
Abnormal Claisen rearrangement
Eschenmoser-Claisen amide acetal rearrangement
Ireland--Claisen (silyl ketene acetal) rearrangement
Johnson-Claisen (orthoester) rearrangement
Clemmensen reduction
Combes quinoline synthesis
Conrad-Limpach reaction
Cope elimination reaction
Cope rearrangement
Oxy-Cope rearrangement
Anionic oxy-Cope rearrangement
Corey-Bakshi-Shibata (CBS) reduction
Corey--Chaykovsky reaction
Corey-Fuchs reaction
Corey-Kim oxidation
Corey-Nicolaou macrolactonization
Corey-Seebach dithiane reaction
Corey-Winter olefin synthesis
Criegee glycol cleavage
Criegee mechanism of ozonolysis
Curtius rearrangement
Dakin oxidation
Dakin-West reaction
Danheiser annulation
Darzens glycidic ester condensation
Davis chiral oxaziridine reagent
Delepine amine synthesis
de Mayo reaction
Demjanov rearrangement
Tiffeneau-Demjanov rearrangement
Dess-Martin oxidation
Dieckmann condensation
Diels-Alder reaction
Dienone-phenol rearrangement
Di-π-methane rearrangement
Doebner quinoline synthesis
Dptz reaction
Dowd-Beckwith ring expansion
Edenmeyer-Plochl azlactone synthesis
Eschenmoser-Tanabe fragmentation
Eschweiler-Clarke reductive alkylation of amines
Evans aldol reaction
Favorskii rearrangement and quasi-Favorskii rearrangement
Feist-Benary furan synthesis
Ferrier carbocyclization
Ferrier glycal allylic rearrangement
Fiesselmann thiophene synthesis
Fischer indole synthesis
Fischer oxazole synthesis
Fleming-Tamao oxidation
Tamao-Kumada oxidation
Friedel-Crafts reaction
Friedlander quinoline synthesis
Fries rearrangement
Fukuyama amine synthesis
Fukuyama reduction
Gabriel synthesis
Ing-Manske procedure
Gabriel-Colman rearrangement
Gassman indole synthesis
Gattermann-Koch reaction
Gewald aminothiophene synthesis
Glaser coupling
Eglinton coupling
Gomberg-Bachmann reaction
Gould-Jacobs reaction
Grignard reaction
Grob fragmentation
Guareschi-Thorpe condensation
Hajos-Wiechert reaction
Hailer-Bauer reaction
Hantzsch dihydropyridine synthesis
Hantzsch pyrrole synthesis
Heck reaction
Heteroaryl Heck reaction
Hegedus indole synthesis
Hell-Volhard-Zelinsky reaction
Henry nitroaldol reaction
Hinsberg synthesis of thiophene derivatives
Hiyama cross-coupling reaction
Hiyama-Denmark cross-coupling reaction
Hofmann rearrangement
Hofmann-Loffler-Freytag reaction
Horner-Wadsworth-Emmons reaction
Houben-Hoesch synthesis
Hunsdiecker-Borodin reaction
Hurd-Mori 1,2,3-thiadiazole synthesis
Jacobsen-Katsuki epoxidation
Japp--Klingemann hydrazone synthesis
Jones oxidation
Julia-Kocienski olefination
Julia-Lythgoe olefination
Kahne--Crich glycosidation
Keck macrolactonization
Knoevenagel condensation
Knorr pyrazole synthesis
Paal-Knorr pyrrole synthesis
Koch-Haaf carbonylation
Koenig-Knorr glycosidation
Kolbe-Schmitt reaction
Kostanecki reaction
Krohnke pyridine synthesis
Kumada cross-coupling reaction
Lawesson's reagent
Leuckart-Wallach reaction
Lossen rearrangement
McFadyen-Stevens reduction
McMurry coupling
MacMillan catalyst
Mannich reaction
Marshall boronate fragmentation
Martin's sulfurane dehydrating reagent
Masamune-Roush conditions
Meerwein-Ponndorf-Verley reduction
Meisenheimer complex
[1,2]-Meisenheimer rearrangement
[2,3]-Meisenheimer rearrangement
Meth-Cohn quinoline synthesis
Meyers oxazoline method
Meyer-Schuster rearrangement
Michael addition
Michaelis-Arbuzov phosphonate syathesis
Midland reduction
Mislow-Evans rearrangement
Mitsunobu reaction
Miyaura borylation
Moffatt oxidation
Montgomery coupling
Morgan-Walls reaction
Pictet-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 reaction
Nenitzescu indole synthesis
Nicholas reaction
Nicolaou dehydrogenation
Nicolaou hydroxy-dithioketal cyelization
Nicolaou hydroxy-ketone reduction
Nicolaou oxyselenation
Noyori asymmetric hydrogenation
Nozaki-Hiyama-Kishi reaction
Oppenauer oxidation
Overman rearrangement
Paal thiophene synthesis
Paal-Knorr furan synthesis
Parham cyclization
Passerini reaction
Patemt-Buchi reaction
Pauson-Khand cyclopentenone synthesis
Payne rearrangement
Pechmann coumarin synthesis
Perkin reaction
Petasis reaction
Peterson olefination
Pictet--Gams isoquinoline synthesis
Pictet-Spengler tetrahydroisoquinoli
Pinacol rearrangement
Pinner reaction
Polonovski reaction
Polonovski-Potier rearrangement
Pomeranz-Fritsch reaction
Schlittler-M011er modification
Prevost trans-dihydroxylation
Woodward cis-dihydroxylation
Prins reaction
Pschorr cyclization
Pummerer rearrangement
Ramberg-Baicklund reaction
Reformatsky reaction
Regitz diazo synthesis
Reimer-Tiemann reaction
Reissert aldehyde synthesis
Reissert indole synthesis
Ring-closing metathesis
Ritter reaction
Robinson annulation
Robinson-Gabriel synthesis
Robinson-Schopf reaction
Rosenmund reduction
Rubottom oxidation
Rupe rearrangement
Saegusa oxidation
Sakurai allylation reaction
Sandmeyer reaction
Schiemann reaction
Schmidt reaction
Schmidt's trichloroacetimidate glycosidation reaction
Shapiro reaction
Sharpless asymmetric amino hydroxylation
Sharpless asymmetric epoxidation
Sharpless asymmetric dihydroxylation
Sharpless olefin synthesis
Simmons-Smith reaction
Skraup quinoline synthesis
Doebner-von Miller reaction
Smiles rearrangement
Newman-Kwart reaction
Truce-Smile rearrangement
Sommelet reaction
Sommelet-Hauser rearrangement
Sonogashira reaction
Staudinger ketene cycloaddition
Staudinger reduction
Stembach benzodiazepine synthesis
Stetter reaction
Still-Gennari phosphonate reaction
Stille coupling
Stille-Kelly reaction
Stobbe condensation
Stork enamine reaction
Strecker amino acid synthesis
Suzuki coupling.
Swem oxidation
Takai iodoalkene synthesis
Tebbe olefination
Petasis alkenylation
TEMPO-mediated oxidation
Thorpe-Ziegler reaction
Tsuji-Trost allylation
Ugi reaction
Ullmann reaction
van Leusen oxazole synthesis
Vilsmeier-Haack reaction
Vilsmeier mechanism for acid chloride formation
Vinylcyclopropane-cyclopentene rearrangement
von Braun reaction
Wacker oxidation
Wagner-Meerwein rearrangement
Weiss-Cook reaction
Wharton oxygen transposition reaction
Willgerodt-Kindler reaction
Wittig reaction
Schlosser modification of the Wittig reaction
[ 1,2]-Wittig rearrangement
[2,3]-Wittig rearrangement
Wohl-Ziegler reaction
Wolff rearrangement
Wolff-Kishner reduction
Yamaguchi esterification
Zincke reaction
Subject Index