Free download 100 Must-Know Mechanisms in Organic Chemistry authored by Roman A. Valiulin in pdf.
This book summarizes 100 essential mechanisms in organic chemistry ranging from classical such as the Reformatsky Reaction from 1887 to recently elucidated mechanism such as the copper(I)-catalyzed alkyne-azide cycloaddition. The reactions are easy to grasp, well-illustrated and underpinned with explanations and additional information.
Contents
- Electrophilic Addition Mechanism
- Nucleophilic Substitution Mechanism
- Aromatic Electrophilic Substitution Mechanism
- Aromatic Nucleophilic Substitution Mechanism
- Aromatic Radical Nucleophilic Substitution Mechanism
- Elimination Mechanism
- Acyloin Condensation
- Alkyne Zipper Reaction
- Arbuzov Reaction
- Arndt‒Eistert Synthesis
- Baeyer‒Villiger Oxidation
- Barton Decarboxylation
- Baylis‒Hillman Reaction
- Beckmann Rearrangement
- Benzoin Condensation
- Benzyne Mechanism
- Bergman Cyclization
- Birch Reduction
- Bischler‒Napieralski Cyclization
- Brown Hydroboration
- Buchwald‒Hartwig Cross Coupling
- Cannizzaro Reaction
- Chan‒Evans‒Lam Cross Coupling
- Chichibabin Amination
- Claisen Condensation
- Claisen Rearrangement
- Cope Elimination
- Cope Rearrangement
- Criegee & Malaprade Oxidation
- CuAAC
- Curtius Rearrangement
- Darzens Condensation
- Dess‒Martin Oxidation
- Diazotization (Diazonium Salt)
- Diels‒Alder Cycloaddition
- Di‒π‒Methane Rearrangement
- Favorskii Rearrangement
- Fischer Indole Synthesis
- Friedel‒Crafts Acylation & Alkylation
- Gabriel Synthesis
- Gewald Reaction
- Glaser–Eglinton–Hay Coupling
- Grignard Reaction
- Grob Fragmentation
- Haloform Reaction
- Heck Cross Coupling
- Hell–Volhard–Zelinsky Reaction
- Hiyama Cross Coupling
- Hofmann Elimination
- Horner–Wadsworth–Emmons Olefination
- Jones Oxidation
- Kucherov Reaction
- Kumada Cross Coupling
- Ley–Griffith Oxidation
- Liebeskind–Srogl Cross Coupling
- Mannich Reaction
- McMurry Coupling
- Meerwein–Ponndorf–Verley Reduction
- Michael Addition
- Minisci Reaction
- Mitsunobu Reaction
- Miyaura Borylation
- Mukaiyama RedOx Hydration
- Nazarov Cyclization
- Nef Reaction
- Negishi Cross Coupling
- Norrish Type I & II Reaction
- Olefin (Alkene) Metathesis
- Oppenauer Oxidation
- Ozonolysis
- Paal–Knorr Syntheses
- Paternò–Büchi Reaction
- Pauson–Khand Reaction
- Peptide (Amide) Coupling
- Pictet–Spengler Reaction
- Pinacol–Pinacolone Rearrangement
- Polonovski Reaction
- Prilezhaev Epoxidation
- Prins Reaction
- Pummerer Rearrangement
- Ramberg–Bäcklund Rearrangement
- Reformatsky Reaction
- Robinson Annulation
- Shapiro Reaction
- Sonogashira Cross Coupling
- Staudinger Reaction
- Steglich Esterification
- Stille Cross Coupling
- Suzuki Cross Coupling
- Swern Oxidation
- Ugi Reaction
- Ullmann Aryl–Aryl Coupling
- Upjohn Dihydroxylation
- Vilsmeier–Haack Reaction
- Wacker Oxidation
- Wagner–Meerwein Rearrangement
- Weinreb Ketone Synthesis
- Wittig Reaction
- Wohl–Ziegler Reaction
- Wolff–Kishner Reduction
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