{"product_id":"carbocation-chemistry-9781498729086","title":"Carbocation Chemistry","description":"\u003cb\u003eBook Synopsis\u003c\/b\u003e\u003cbr\u003eCarbocation chemistry is not only fundamental to the advancement of organic chemistry, it also has found widespread applications in organic synthesis. It is not an exaggeration to say that carbocation chemistry is part of the foundation of organic chemistry. \u003ci\u003eCarbocation Chemistry: Applications in Organic Synthesis\u003c\/i\u003e provides a panoramic view of carbocation chemistry with an emphasis on synthetic applications. \u003cp\u003eThis book is an invaluable tool for organic, medicinal and analytical chemists, including those working in biochemistry as well as the petroleum, plastics and pharmaceutical industries. It is also suitable for upper level undergraduates and graduates in organic chemistry, biochemistry and medicinal chemistry.\u003c\/p\u003e\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTable of Contents\u003c\/b\u003e\u003cbr\u003e\u003cp\u003e\u003cstrong\u003eChapter 1. Introduction\u003c\/strong\u003e \u003c\/p\u003e\u003col\u003e\n\u003cli\u003eNomenclature, Structure, and Stability\u003c\/li\u003e\n\u003cli\u003eGeneration of Carbocations\u003c\/li\u003e\n\u003cli\u003eThe Non-Classical Ion Controversy\u003c\/li\u003e\n\u003cli\u003eElectrophilic Addition to Alkenes\u003c\/li\u003e\n\u003cli\u003eElectrophilic Aromatic Substitution\u003c\/li\u003e\n\u003cli\u003eElimination reactions\u003c\/li\u003e\n\u003cli\u003eRearrangement Reactions of Carbocations\u003c\/li\u003e\n\u003cli\u003eReferences\u003c\/li\u003e\n\u003c\/ol\u003e\u003cp\u003e\u003cstrong\u003eChapter 2. Nucleophilic Aliphatic Substitution – SN1\u003c\/strong\u003e \u003c\/p\u003e\u003col\u003e\n\u003cli\u003eIntroduction\u003c\/li\u003e\n\u003cli\u003e-Activated Alcohols—Brønsted Acids\u003c\/li\u003e\n\u003cli\u003e-Activated Alcohols—Lewis Acids\u003c\/li\u003e\n\u003cli\u003eAlkylation of Aldehydes and Ketones\u003c\/li\u003e\n\u003cli\u003eGlycosylation \u003c\/li\u003e\n\u003cli\u003eFriedel–Crafts Alkylation and Acylation \u003c\/li\u003e\n\u003cli\u003eElectrophilic Fluorination Using Fluoronium Ion\u003c\/li\u003e\n\u003cli\u003eMiscellaneous SN1-related Reactions\u003c\/li\u003e\n\u003cli\u003eReferences\u003c\/li\u003e\n\u003c\/ol\u003e\u003cp\u003e\u003cstrong\u003eChapter 3. Nucleophilic Aliphatic Substitution – SN2\u003c\/strong\u003e \u003c\/p\u003e\u003col\u003e\n\u003cli\u003eConstruction of Quaternary Stereogenic Centers\u003c\/li\u003e\n\u003cli\u003eSulfur Chemistry\u003c\/li\u003e\n\u003cli\u003eOrganometallic Chemistry\u003c\/li\u003e\n\u003cli\u003eMacrocyclization\u003c\/li\u003e\n\u003cli\u003eGlycosylation\u003c\/li\u003e\n\u003cli\u003eNucleoside Analogues\u003c\/li\u003e\n\u003cli\u003e \u003ci\u003eN\u003c\/i\u003e-Alkylation\u003c\/li\u003e\n\u003cli\u003eCyclotetraphosphazenes\u003c\/li\u003e\n\u003cli\u003eConformationally Locked Tetrahydropyran Ring\u003c\/li\u003e\n\u003cli\u003eThe Ionic Liquid Effect\u003c\/li\u003e\n\u003cli\u003eSilver Chemistry\u003c\/li\u003e\n\u003cli\u003eReferences\u003c\/li\u003e\n\u003c\/ol\u003e\u003cp\u003e\u003cstrong\u003eChapter 4. Electrophilic Addition to Alkenes\u003c\/strong\u003e \u003c\/p\u003e\u003col\u003e\n\u003cli\u003eIntroduction\u003c\/li\u003e\n\u003cli\u003eCyclopropanation\u003c\/li\u003e\n\u003cli\u003eHydroboration\/Oxidation\u003c\/li\u003e\n\u003cli\u003eThe Pauson–Khand Reaction\u003c\/li\u003e\n\u003cli\u003ePrins Reaction\u003c\/li\u003e\n\u003cli\u003eSchmidt Reaction\u003c\/li\u003e\n\u003cli\u003eHalogenation\u003c\/li\u003e\n\u003cli\u003eOxymercuration\/Reduction\u003c\/li\u003e\n\u003cli\u003eEpoxidation\u003c\/li\u003e\n\u003cli\u003eGold-Catalyzed Alkyne Hydration\u003c\/li\u003e\n\u003cli\u003eConclusion\u003c\/li\u003e\n\u003cli\u003eReferences\u003c\/li\u003e\n\u003c\/ol\u003e\u003cp\u003e\u003cstrong\u003eChapter 5. Electrophilic Aromatic Substitution\u003c\/strong\u003e \u003c\/p\u003e\u003col\u003e\n\u003cli\u003eIntroduction\u003c\/li\u003e\n\u003cli\u003eNitration\u003c\/li\u003e\n\u003cli\u003eHalogenation\u003c\/li\u003e\n\u003cli\u003eFriedel–Crafts Alkylation\u003c\/li\u003e\n\u003cli\u003eFriedel–Crafts Acylation\u003c\/li\u003e\n\u003cli\u003eApplications of Friedel–Crafts Reaction on Total Synthesis\u003c\/li\u003e\n\u003cli\u003eMiscellaneous Electrophilic Aromatic Substitution Reactions\u003c\/li\u003e\n\u003cli\u003eReferences\u003c\/li\u003e\n\u003c\/ol\u003e\u003cp\u003e\u003cstrong\u003eChapter 6. Fragmentation and Rearrangement Reactions\u003c\/strong\u003e \u003c\/p\u003e\u003col\u003e\n\u003cli\u003eClaisen Rearrangements\u003c\/li\u003e\n\u003cli\u003eCope Rearrangements\u003c\/li\u003e\n\u003cli\u003eCope Rearrangements\u003c\/li\u003e\n\u003cli\u003eAldehyde (or Ketone) Formation Rearrangements\u003c\/li\u003e\n\u003cli\u003eCarboxylic Acid Formation Rearrangements\u003c\/li\u003e\n\u003cli\u003eAlcohol Formation Rearrangements \u003c\/li\u003e\n\u003cli\u003eAmine Formation Rearrangement \u003c\/li\u003e\n\u003cli\u003eAmides\u003c\/li\u003e\n\u003cli\u003eHydrocarbon Rearrangements\u003c\/li\u003e\n\u003cli\u003eOxacyclic, Carbocyclic, Oxazoles, Tetrahydrapuran and Tetrahydropuran Formation Rearrangements\u003c\/li\u003e\n\u003cli\u003eRearrangements resulting in less common functional groups \u003c\/li\u003e\n\u003cli\u003eFragmentations\u003c\/li\u003e\n\u003cli\u003eReferences\u003c\/li\u003e\n\u003c\/ol\u003e","brand":"Taylor \u0026 Francis Inc","offers":[{"title":"Default Title","offer_id":49409284276567,"sku":"9781498729086","price":175.75,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0817\/1739\/5799\/files\/9781498729086.jpg?v=1730506282","url":"https:\/\/bookcurl.com\/products\/carbocation-chemistry-9781498729086","provider":"Book Curl","version":"1.0","type":"link"}