{"product_id":"s-triazines-and-derivatives-volume-13-hardback-9780470378847","title":"s-Triazines and Derivatives, Volume 13 (Hardback) 9780470378847","description":"\u003cfont face=\"Georgia\"\u003e\r\n\u003cp\u003e\u003cfont size=\"6\"\u003es-Triazines and Derivatives, Volume 13\u003c\/font\u003e\u003cbr\u003e\r\n\r\n\r\n\r\n\r\n\r\n\u003c\/p\u003e\n\u003cp\u003e\u003cfont size=\"4\"\u003eEdwin M. Smolin (Edited by), Smolin (Author), Lorence Rapoport (Edited by)\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e9780470378847, Wiley\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eHardback, published 1 January 1959\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e672 pages\u003cbr\u003e23.6 x 16.7 x 4.5 cm, 1.106 kg\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\r\n\r\n\r\n\u003cp align=\"justify\"\u003e\u003cstrong\u003e\u003cfont size=\"3\"\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.\u003c\/font\u003e\u003c\/strong\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e\u003cp\u003eIntroduction 1\u003c\/p\u003e \u003cp\u003e\u003cb\u003eI. Cyanuric Acid and Derivatives 17\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eI. Introduction 17\u003c\/p\u003e \u003cp\u003eII. Cyanunc Acid 20\u003c\/p\u003e \u003cp\u003eIII. Cyanuric Halides 48\u003c\/p\u003e \u003cp\u003eIV. Cyanuric Acid Esters 67\u003c\/p\u003e \u003cp\u003eV. Acyloxy-\u003ci\u003es\u003c\/i\u003e-triazines 90\u003c\/p\u003e \u003cp\u003eVI. Cyanuric Azides 100\u003c\/p\u003e \u003cp\u003eVII. Thiocyanuric Acids 105\u003c\/p\u003e \u003cp\u003eVIII. Triazinylthioglycolic Acids and Their Derivatives 114\u003c\/p\u003e \u003cp\u003eIX. 2.4.6-Tri(acetonylthio).s.triazine 115\u003c\/p\u003e \u003cp\u003eX. Triselenocyanuric Acid 116\u003c\/p\u003e \u003cp\u003eXI. Esters of s-Triazine-2,4.6-triphosphonite 117\u003c\/p\u003e \u003cp\u003eXII. Uses and Industrial Applications of Cyanuric Chloride and Derivatives 117\u003c\/p\u003e \u003cp\u003e\u003cb\u003eII\u003c\/b\u003e. \u003cb\u003eAlkyl(Ary1)-\u003ci\u003es\u003c\/i\u003e-triazines 147\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eI. Introduction 147\u003c\/p\u003e \u003cp\u003eII. General Synthetic Methods 149\u003c\/p\u003e \u003cp\u003eIII. Reactions 162\u003c\/p\u003e \u003cp\u003eIV. Trialkyl-s-Triazines 165\u003c\/p\u003e \u003cp\u003eV. Triaryl-s-triazines 171\u003c\/p\u003e \u003cp\u003eVI. Alkyl-aryl-s-Triazines 179\u003c\/p\u003e \u003cp\u003eVII. Alkyl-aryl-dihydro-\u003ci\u003es\u003c\/i\u003e-triazines 179\u003c\/p\u003e \u003cp\u003eVIII. Applications 182\u003c\/p\u003e \u003cp\u003e\u003cb\u003eIII.\u003c\/b\u003e \u003cb\u003eMonohydroxy-, Hydroxyamino-, Dihydroxy-\u003ci\u003es\u003c\/i\u003e-triazines and Related Compounds 185\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eI. Monohydroxy-s-triazines 185\u003c\/p\u003e \u003cp\u003eII. Monochloro-s-triazines 185\u003c\/p\u003e \u003cp\u003eIII. Hydroxyamino-s-triazines 187\u003c\/p\u003e \u003cp\u003eIV. Dihydroxy-s-triazines 202\u003c\/p\u003e \u003cp\u003eV. Hydrogenated Derivatives 209\u003c\/p\u003e \u003cp\u003eVI. Dihalo-s-triazines 214\u003c\/p\u003e \u003cp\u003e\u003cb\u003elV.\u003c\/b\u003e \u003cb\u003eMonoamino- and Diamino-\u003ci\u003es\u003c\/i\u003e-triazines 217\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eI. Monoamino-s-triazines 217\u003c\/p\u003e \u003cp\u003eII. Diamino-s-triazines 222\u003c\/p\u003e \u003cp\u003eIII. Diamino dihydro-s-triazines 258\u003c\/p\u003e \u003cp\u003e\u003cb\u003eV. Ammelide. Ammeline. and Related Compounds 269\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eI. Ammelide 269\u003c\/p\u003e \u003cp\u003eII. Ammelide Ethers 274\u003c\/p\u003e \u003cp\u003eIII. Aminodichloro-\u003ci\u003es\u003c\/i\u003e-triazines 279\u003c\/p\u003e \u003cp\u003eIV.Ammeline 281\u003c\/p\u003e \u003cp\u003eV. Ammeline Ethers 285\u003c\/p\u003e \u003cp\u003eVI. Diaminochloro-s-triazines 292\u003c\/p\u003e \u003cp\u003eVII. Dithioammelide 297\u003c\/p\u003e \u003cp\u003eVIII. Thioammeline 298\u003c\/p\u003e \u003cp\u003eIX. Thioammeline Ethers 301\u003c\/p\u003e \u003cp\u003eX. Related Compounds 305\u003c\/p\u003e \u003cp\u003e\u003cb\u003eVI. Melamine and Substituted Melamines 309\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eI. Introduction 309\u003c\/p\u003e \u003cp\u003eII. Physical Properties 309\u003c\/p\u003e \u003cp\u003eIII. Synthesis of Melamine 309\u003c\/p\u003e \u003cp\u003eIV. Reactions of Melamine 321\u003c\/p\u003e \u003cp\u003eV. Structure 348\u003c\/p\u003e \u003cp\u003eVI. Substituted \"Normal\" Melamines 349\u003c\/p\u003e \u003cp\u003eVII. Applications of Melamine and Derivatives 373\u003c\/p\u003e \u003cp\u003eVIII. IsomelaminES 379\u003c\/p\u003e \u003cp\u003e\u003cb\u003eVII\u003c\/b\u003e. \u003cb\u003eIsocyanuric Acid and Derivatives 389\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eI. Isocyanuric Acid 389\u003c\/p\u003e \u003cp\u003eII. 1.3.5.Trihalo.2.4.6.trioxohexahydro-\u003ci\u003es\u003c\/i\u003e-triazines 390\u003c\/p\u003e \u003cp\u003eIII. Esters ofIsocyanuric Acid 393\u003c\/p\u003e \u003cp\u003eIV. Isothiocyanuric Acid 416\u003c\/p\u003e \u003cp\u003eV. Other Isocyanuric Compounds 420\u003c\/p\u003e \u003cp\u003e\u003cb\u003eVIII.\u003c\/b\u003e \u003cb\u003eCondensed Ring \u003ci\u003es\u003c\/i\u003e-Triazine Systems 423\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eI.Endo Compounds 423\u003c\/p\u003e \u003cp\u003eII. Condensed Five-Membered Ring Compounds 426\u003c\/p\u003e \u003cp\u003eIII. Condensed-Six-Membered Ring Compounds 445\u003c\/p\u003e \u003cp\u003e\u003cb\u003eIX.\u003c\/b\u003e \u003cb\u003eHexahydro-\u003ci\u003es\u003c\/i\u003e-triazines 473\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eI. Introduction 473\u003c\/p\u003e \u003cp\u003eII. Hexahydro-s-triazine and Nitrate 473\u003c\/p\u003e \u003cp\u003eIII. 1.3.5.Trialkylhexahydro-\u003ci\u003es-\u003c\/i\u003etriazine 476\u003c\/p\u003e \u003cp\u003eIV. Aryl and Arylalkylhexahydro-\u003ci\u003es\u003c\/i\u003e-triazines 490\u003c\/p\u003e \u003cp\u003eV. 2.4,6-Trialkyl- and Triarylhexahydro-\u003ci\u003es\u003c\/i\u003e-triazines 505\u003c\/p\u003e \u003cp\u003eVI. Halogen Derivatives of Hexahydro-s-triazine and Alkylhexahydro-\u003ci\u003es\u003c\/i\u003e-triazines 506\u003c\/p\u003e \u003cp\u003eVII. Nitro- and Nitrosohexahydro-\u003ci\u003es\u003c\/i\u003e-triazines 509\u003c\/p\u003e \u003cp\u003eVIII. Amino Derivatives of Hexahydro-s-triazines 526\u003c\/p\u003e \u003cp\u003eIX. Sulfonyl Derivatives 528\u003c\/p\u003e \u003cp\u003eX. Hydroxy Derivatives: 1.3.5-Trihydroxyhexahydro-\u003ci\u003es\u003c\/i\u003e-triazines 1,3,5-Trinitrosohexahydros-\u003ci\u003es\u003c\/i\u003e-triazines 531\u003c\/p\u003e \u003cp\u003eXI. Carbonyl (Acyl) Derivatives 533\u003c\/p\u003e \u003cp\u003eXII. Oxo and Thion Derivatives 536\u003c\/p\u003e \u003cp\u003eXIII. Carboxylic Acid Derivatives 539\u003c\/p\u003e \u003cp\u003eXIV. 1-Sulfo-4-alkylhexahydro.2,4,6-triazines 540\u003c\/p\u003e \u003cp\u003e\u003cb\u003eX. Hexamethylenetetramine 545\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eI. Introduction 545\u003c\/p\u003e \u003cp\u003eII. Structure 545\u003c\/p\u003e \u003cp\u003eIII. Formation 546\u003c\/p\u003e \u003cp\u003eIV. Physical Properties 550\u003c\/p\u003e \u003cp\u003eV. Preparation 551\u003c\/p\u003e \u003cp\u003eVI. Reactions 552\u003c\/p\u003e \u003cp\u003eVII. Detection and Analysis of Hexamethylenetetramie 588\u003c\/p\u003e \u003cp\u003eVIII. Uses of Hexamethylenetetramine 588\u003c\/p\u003e \u003cp\u003e\u003cb\u003eXI.\u003c\/b\u003e \u003cb\u003e\u003ci\u003es\u003c\/i\u003e-Triazaborane and Its Derivatives 597\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eI. Introduction 597\u003c\/p\u003e \u003cp\u003eII. \u003ci\u003es\u003c\/i\u003e-Triazaborane 597\u003c\/p\u003e \u003cp\u003eIII. Alkyl Derivatives of \u003ci\u003es\u003c\/i\u003e-Triazaborane 607\u003c\/p\u003e \u003cp\u003eIV. Halogen Derivatives of \u003ci\u003es\u003c\/i\u003e-Triazaborane 619\u003c\/p\u003e \u003cp\u003eV. Hydroxy-s-triazaboranes 624\u003c\/p\u003e \u003cp\u003eVI. Methoxy-s-triazaboranes 624\u003c\/p\u003e \u003cp\u003eVII. Other s-Triazaborane Derivatives 625\u003c\/p\u003e\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eSubject Areas: Chemistry [\u003ca title=\"See our other books on Chemistry\" href=\"https:\/\/freshlyprintedbooks.co.uk\/search?q=%22Chemistry%20%5BPN%5D%22\"\u003ePN\u003c\/a\u003e]\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\u003c\/font\u003e","brand":"Wiley-Interscience","offers":[{"title":"Brand New","offer_id":52276212990232,"sku":"9780470378847","price":421.76,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0730\/2037\/5320\/files\/9780470378847.jpg?v=1781365231","url":"https:\/\/freshlyprintedbooks.co.uk\/products\/s-triazines-and-derivatives-volume-13-hardback-9780470378847","provider":"Freshly Printed Books","version":"1.0","type":"link"}