{"product_id":"pyridine-and-its-derivatives-volume-14-part-2-9780470379509","title":"Pyridine and Its Derivatives Volume 14 Part 2","description":"\u003cb\u003eBook Synopsis\u003c\/b\u003e\u003cbr\u003eThe \u003ci\u003eChemistry of Heterocyclic Compounds\u003c\/i\u003e, since its inception, has been recognized as a cornerstone of heterocyclic chemistry. Each volume attempts to discuss all aspects  properties, synthesis, reactions, physiological and industrial significance  of a specific ring system. To keep the series up-to-date, supplementary volumes covering the recent literature on each individual ring system have been published. Many ring systems (such as pyridines and oxazoles) are treated in distinct books, each consisting of separate volumes or parts dealing with different individual topics. With all authors are recognized authorities, the \u003ci\u003eChemistry of Heterocyclic Chemistry\u003c\/i\u003e is considered worldwide as the indispensable resource for organic, bioorganic, and medicinal chemists.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTable of Contents\u003c\/b\u003e\u003cbr\u003e\u003cp\u003e\u003cb\u003eIII. Quaternary Pyridinium Compounds 1\u003cbr\u003e\u003c\/b\u003eBy \u003ci\u003eElliott \u003c\/i\u003e\u003ci\u003eN\u003c\/i\u003e. \u003ci\u003eShaw\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eB. Properties and Reactions 31\u003c\/p\u003e \u003cp\u003eC Pyridinium Compounds of Biological Interest 80\u003c\/p\u003e \u003cp\u003e\u003cb\u003eIV.\u003c\/b\u003e\u003cb\u003e Pyridine \u003ci\u003eN\u003c\/i\u003e-Oxides 97\u003cbr\u003e\u003c\/b\u003eBy \u003ci\u003eElliott N.\u003c\/i\u003e \u003ci\u003eShaw\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eA. Preparation 98\u003c\/p\u003e \u003cp\u003eB. Properties 117\u003c\/p\u003e \u003cp\u003eC. Reactions 120\u003c\/p\u003e \u003cp\u003eD. Aminopyridine I-Oxides 133\u003c\/p\u003e \u003cp\u003eE. Pyridinol I-Oxides (N-Hydroxypyridones) 134\u003c\/p\u003e \u003cp\u003eF. l-Aminopyridinium Salts and Pyridine Arylimines 143\u003c\/p\u003e \u003cp\u003e\u003cb\u003eV.\u003c\/b\u003e\u003cb\u003e Alkylpyridims and Arylpyridines 155\u003cbr\u003e\u003c\/b\u003eBy \u003ci\u003eLeon \u003c\/i\u003e\u003ci\u003eE\u003c\/i\u003e. \u003ci\u003eTenenbarrm\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eA. Alkyl and Aralkylpyridines 157\u003c\/p\u003e \u003cp\u003eB. Alkenyl and Aralkenylpyridines 199\u003c\/p\u003e \u003cp\u003eC. Alkynyl and Aralkynylpyridines 213\u003c\/p\u003e \u003cp\u003eD. Di- and Polypyridylalkanes and Alkenes 215\u003c\/p\u003e \u003cp\u003eE. Arylpyridines 216\u003c\/p\u003e \u003cp\u003eF. Bi- and Polypyridines 224\u003c\/p\u003e \u003cp\u003eG. Tables 231\u003c\/p\u003e \u003cp\u003e\u003cb\u003eVI.\u003c\/b\u003e\u003cb\u003e Halopyridines 299\u003cbr\u003e\u003c\/b\u003eBy \u003ci\u003eHolly\u003c\/i\u003e \u003ci\u003eE.\u003c\/i\u003e \u003ci\u003eMertei\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eA. Introduction 300\u003c\/p\u003e \u003cp\u003eB. Nuclear Halogen Derivatives 301\u003c\/p\u003e \u003cp\u003eC. Side-Chain Halogen Derivatives 360\u003c\/p\u003e \u003cp\u003eD. Tables 371\u003c\/p\u003e \u003cp\u003e\u003cb\u003eVII.\u003c\/b\u003e\u003cb\u003e Organometallic Compounds of Pyridine 421\u003cbr\u003e\u003c\/b\u003eBy \u003ci\u003eHurry\u003c\/i\u003e \u003ci\u003eL.\u003c\/i\u003e \u003ci\u003eYale\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eA. Lithium Compounds 422\u003c\/p\u003e \u003cp\u003eB. Sodium Compounds 432\u003c\/p\u003e \u003cp\u003eC. Potassium Compounds 435\u003c\/p\u003e \u003cp\u003eD. Grignard Cornpounds 437\u003c\/p\u003e \u003cp\u003eE. Mercury Compounds 440\u003c\/p\u003e \u003cp\u003eF. Thallium Compounds 443\u003c\/p\u003e \u003cp\u003eG. Tin Compounds 443\u003c\/p\u003e \u003cp\u003eH. Lead Compounds 444\u003c\/p\u003e \u003cp\u003eI. Silicon Compounds 444\u003c\/p\u003e \u003cp\u003eJ. Tables 445\u003c\/p\u003e \u003cp\u003e\u003cb\u003eVIII.\u003c\/b\u003e\u003cb\u003e Nitropvridines and Their Reduction Products (except Amines) 469\u003cbr\u003e\u003c\/b\u003eBy \u003ci\u003eRenat H.\u003c\/i\u003e \u003ci\u003eMiuoni\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eA. Nitropyridines 470\u003c\/p\u003e \u003cp\u003eB. Nitrosopyridines 481\u003c\/p\u003e \u003cp\u003eC\u003ci\u003e.\u003c\/i\u003e Hydroxylaminopyridines 482\u003c\/p\u003e \u003cp\u003eD. Azopyridines 483\u003c\/p\u003e \u003cp\u003eE. Azoxypyridines 488\u003c\/p\u003e \u003cp\u003eF. Hydrazinopyridines 488\u003c\/p\u003e \u003cp\u003eG\u003ci\u003e.\u003c\/i\u003e Hydrazopyridines 492\u003c\/p\u003e \u003cp\u003eH. Pyridyl Azides 493\u003c\/p\u003e \u003cp\u003eI. Side-Chain Derivatives 493\u003c\/p\u003e \u003cp\u003eJ. Tables 496\u003c\/p\u003e \u003cp\u003eSubject Index 547\u003c\/p\u003e","brand":"John Wiley \u0026 Sons Inc","offers":[{"title":"Default Title","offer_id":53515416338775,"sku":"9780470379509","price":460.76,"currency_code":"GBP","in_stock":true}],"url":"https:\/\/bookcurl.com\/products\/pyridine-and-its-derivatives-volume-14-part-2-9780470379509","provider":"Book Curl","version":"1.0","type":"link"}