دانلود کتاب Organic Chemistry: 100 Must-Know Mechanisms

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Second Edition\nPreface and Overview\nContents\nList of Acronyms and Abbreviations\n1 Electrophilic Addition Mechanism\n2 Nucleophilic Substitution Mechanism\n3 Aromatic Electrophilic Substitution Mechanism \n4 Aromatic Nucleophilic Substitution Mechanism\n5 Aromatic Radical Nucleophilic Substitution Mechanism\n6 Elimination Mechanism\n7 Acyloin Condensation\n8 Alkyne Zipper Reaction\n9 Arbuzov Reaction\n10 Arndt–Eistert Synthesis\n11 Baeyer–Villiger Oxidation\n12 Barton Decarboxylation\n13 Baylis–Hillman Reaction\n14 Beckmann Rearrangement\n15 Benzoin Condensation\n16 Benzyne Mechanism\n17 Bergman Cyclization\n18 Birch Reduction\n19 Bischler‒Napieralski Cyclization\n20 Brown Hydroboration\n21 Buchwald–Hartwig Cross-Coupling\n22 Cannizzaro Reaction\n23 Chan–Evans–Lam Cross-Coupling\n24 Chichibabin Amination\n25 Claisen Condensation\n26 Claisen Rearrangement\n27 Cope Elimination\n28 Cope Rearrangement\n29 Criegee and Malaprade Oxidation\n30 CuAAC\n31 Curtius Rearrangement\n32 Darzens Condensation\n33 Dess–Martin Oxidation\n34 Diazotization (Diazonium Salt)\n35 Diels–Alder Cycloaddition\n36 Di-π-Methane Rearrangement\n37 Favorskii Rearrangement\n38 Fischer Indole Synthesis\n39 Friedel–Crafts Acylation and Alkylation\n40 Gabriel Synthesis\n41 Gewald Reaction\n42 Glaser–Eglinton–Hay Coupling\n43 Grignard Reaction\n44 Grob Fragmentation\n45 Haloform Reaction\n46 Heck Cross-Coupling\n47 Hell–Volhard–Zelinsky Reaction\n48 Hiyama Cross-Coupling\n49 Hofmann Elimination\n50 Horner–Wadsworth–Emmons Olefination\n51 Jones Oxidation\n52 Kucherov Reaction\n53 Kumada Cross-Coupling\n54 Ley–Griffith Oxidation\n55 Liebeskind–Srogl Cross-Coupling\n56 Mannich Reaction\n57 McMurry Coupling Fig.\n58 Meerwein–Ponndorf–Verley Reduction\n59 Michael Addition\n60 Minisci Reaction\n61 Mitsunobu Reaction\n62 Miyaura Borylation\n63 Mukaiyama RedOx Hydration\n64 Nazarov Cyclization\n65 Nef Reaction\n66 Negishi Cross-Coupling\n67 Norrish Type I and II Reactions\n68 Olefin (Alkene) Metathesis\n69 Oppenauer Oxidation\n70 Ozonolysis\n71 Paal–Knorr Syntheses\n72 Paternò–Büchi Reaction\n73 Pauson–Khand Reaction\n74 Peptide (Amide) Coupling\n75 Pictet–Spengler Reaction\n76 Pinacol–Pinacolone Rearrangement\n77 Polonovski Reaction\n78 Prilezhaev Epoxidation\n79 Prins Reaction\n80 Pummerer Rearrangement\n81 Ramberg–Bäcklund Rearrangement\n82 Reformatsky Reaction\n83 Robinson Annulation\n84 Shapiro Reaction\n85 Sonogashira Cross-Coupling\n86 Staudinger Reaction\n87 Steglich Esterification\n88 Stille Cross-Coupling\n89 Suzuki Cross-Coupling\n90 Swern Oxidation\n91 Ugi Reaction\n92 Ullmann Aryl–Aryl Coupling\n93 Upjohn Dihydroxylation\n94 Vilsmeier–Haack Reaction\n95 Wacker Oxidation\n96 Wagner–Meerwein Rearrangement Fi\n97 Weinreb Ketone Synthesis\n98 Wittig Reaction\n99 Wohl–Ziegler Reaction\n100 Wolff–Kishner Reduction\nAcknowledgments\nBibliography and References