{"product_id":"fundamentals-of-heterocyclic-chemistry-9780470566695","title":"Fundamentals of Heterocyclic Chemistry","description":"\u003cb\u003eBook Synopsis\u003c\/b\u003e\u003cbr\u003e\u003cul\u003e \u003cli\u003eHeterocyclic chemistry is of prime importance as a sub-discipline of Organic Chemistry, as millions of heterocyclic compounds are known with more being synthesized regularly\u003c\/li\u003e \u003cli\u003eIntroduces students to heterocyclic chemistry and synthesis with practical examples of applied methodology\u003c\/li\u003e \u003cli\u003eEmphasizes natural product and pharmaceutical applications\u003c\/li\u003e \u003cli\u003eProvides graduate students and researchers in the pharmaceutical and related sciences with a background in the field\u003c\/li\u003e \u003cli\u003eIncludes problem sets with several chapters\u003c\/li\u003e \u003c\/ul\u003e\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTrade Review\u003c\/b\u003e\u003cbr\u003e\"Provides graduate students and researchers in the pharmaceutical and related sciences with a background in the field.\" (Trading Charts, 22 February 2011)\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTable of Contents\u003c\/b\u003e\u003cbr\u003e\u003cb\u003ePREFACE.\u003c\/b\u003e  \u003cp\u003e\u003cb\u003eACKNOWLEDGMENT.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 1 THE SCOPE OF THE FIELD OF HETEROCYCLIC CHEMISTRY.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003eAppendix.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 2 COMMON RING SYSTEMS AND THE NAMING OF HETEROCYCLIC COMPOUNDS.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e2.1. General.\u003c\/p\u003e \u003cp\u003e2.2. Naming Simple Monocyclic Compounds.\u003c\/p\u003e \u003cp\u003e2.3. Handling the \"Extra Hydrogen\".\u003c\/p\u003e \u003cp\u003e2.4. Substituted Monocyclic Compounds.\u003c\/p\u003e \u003cp\u003e2.5. Rings With More Than One Heteroatom.\u003c\/p\u003e \u003cp\u003e2.6. Bicyclic Compounds.\u003c\/p\u003e \u003cp\u003e2.7. Multicyclic Systems.\u003c\/p\u003e \u003cp\u003e2.8. The Replacement Nomenclature System.\u003c\/p\u003e \u003cp\u003e2.9. Saturated Bridged Ring Systems.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003eReview Exercises.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 3 NATURE AS A SOURCE OF HETEROCYCLIC COMPOUNDS.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e3.1. General.\u003c\/p\u003e \u003cp\u003e3.2. Naturally Occurring Nitrogen Heterocyclic Compounds.\u003c\/p\u003e \u003cp\u003e3.3. Oxygen Compounds.\u003c\/p\u003e \u003cp\u003e3.4. Sulfur and Phosphorus Heterocyclic Compounds in Nature.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 4 PRINCIPLES OF SYNTHESIS OF AROMATIC HETEROCYCLES BY INTRAMOLECULAR CYCLIZATION.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e4.1. General.\u003c\/p\u003e \u003cp\u003e4.2. Some of the Classic Synthetic Methods.\u003c\/p\u003e \u003cp\u003e4.3. Cyclizations Involving Metallic Complexes as Catalysts.\u003c\/p\u003e \u003cp\u003e4.4. Cyclizations with Radical Intermediates.\u003c\/p\u003e \u003cp\u003e4.5. Cyclizations by Intramolecular Wittig Reactions.\u003c\/p\u003e \u003cp\u003e4.6. Synthesis of Heterocycles by the Alkene Metathesis Reaction.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003eReview Exercises.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 5 SYNTHESIS OF HETEROCYCLIC SYSTEMS BY CYCLOADDITION REACTIONS.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e5.1. The Diels–Alder Reaction.\u003c\/p\u003e \u003cp\u003e5.2. Dipolar Cycloadditions.\u003c\/p\u003e \u003cp\u003e5.3. [2 + 2] Cycloadditions.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003eReview Exercises.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 6 AROMATICITY AND OTHER SPECIAL PROPERTIES OF HETEROCYCLES: PI-DEFICIENT RING SYSTEMS.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e6.1. General.\u003c\/p\u003e \u003cp\u003e6.2. Review of the Aromaticity of Benzene.\u003c\/p\u003e \u003cp\u003e6.3. Pi-Deficient Aromatic Heterocycles.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003eReview Exercises.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 7 AROMATICITY AND OTHER SPECIAL PROPERTIES OF HETEROCYCLES: PI-EXCESSIVE RING SYSTEMS AND MESOIONIC RING SYSTEMS.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e7.1. Pi-Excessive Aromatic Heterocycles.\u003c\/p\u003e \u003cp\u003e7.2. Mesoionic Heterocycles.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003eReview Exercises.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 8 THE IMPORTANCE OF HETEROCYCLES IN MEDICINE.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e8.1. General.\u003c\/p\u003e \u003cp\u003e8.2. Historical.\u003c\/p\u003e \u003cp\u003e8.3. Pyridines.\u003c\/p\u003e \u003cp\u003e8.4. Indoles.\u003c\/p\u003e \u003cp\u003e8.5. Quinolines.\u003c\/p\u003e \u003cp\u003e8.6. Azepines.\u003c\/p\u003e \u003cp\u003e8.7. Pyrimidines.\u003c\/p\u003e \u003cp\u003e8.8. Concluding Remarks.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 9 SYNTHETIC METHODS FOR SOME PROMINENT HETEROCYCLIC FAMILIES: EXAMPLES OF PHARMACEUTICALS SYNTHESIS.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e9.1. Scope of the Chapter.\u003c\/p\u003e \u003cp\u003e9.2. Pyrroles.\u003c\/p\u003e \u003cp\u003e9.3. Furans.\u003c\/p\u003e \u003cp\u003e9.4. Thiophenes.\u003c\/p\u003e \u003cp\u003e9.5. 1,3-Thiazoles.\u003c\/p\u003e \u003cp\u003e9.6. 1,3-Oxazoles.\u003c\/p\u003e \u003cp\u003e9.7. Imidazoles.\u003c\/p\u003e \u003cp\u003e9.8. Pyrazoles.\u003c\/p\u003e \u003cp\u003e9.9. 1,2,4-Triazoles.\u003c\/p\u003e \u003cp\u003e9.10. Tetrazoles.\u003c\/p\u003e \u003cp\u003e9.11. 1,3,4-Thiadiazoles and other 5-Membered Systems.\u003c\/p\u003e \u003cp\u003e9.12. Indole.\u003c\/p\u003e \u003cp\u003e9.13. Pyridines.\u003c\/p\u003e \u003cp\u003e9.14. Quinolines and Isoquinolines.\u003c\/p\u003e \u003cp\u003e9.15. Benzodiazepines.\u003c\/p\u003e \u003cp\u003e9.16. Pyrimidines.\u003c\/p\u003e \u003cp\u003e9.17. Fused Pyrimidines: Purines and Pteridines.\u003c\/p\u003e \u003cp\u003e9.18. 1,3,5-Triazines.\u003c\/p\u003e \u003cp\u003e9.19. Multicyclic Compounds.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003eReview Exercises.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 10 GEOMETRIC AND STEREOCHEMICAL ASPECTS OF NONAROMATIC HETEROCYCLES.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e10.1. General.\u003c\/p\u003e \u003cp\u003e10.2. Special Properties of Three-Membered Rings.\u003c\/p\u003e \u003cp\u003e10.3. Closing Heterocyclic Rings: Baldwin’s Rules.\u003c\/p\u003e \u003cp\u003e10.4. Conformations of Heterocyclic Rings.\u003c\/p\u003e \u003cp\u003e10.5. Chirality Effects on Biological Properties of Heterocycles.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003eReview Exercises.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 11 SYNTHETIC HETEROCYCLIC COMPOUNDS IN AGRICULTURAL AND OTHER APPLICATIONS.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e11.1. Heterocyclic Agrochemicals.\u003c\/p\u003e \u003cp\u003e11.2. Applications of Heterocyclic Compounds in Commercial Fields.\u003c\/p\u003e \u003cp\u003eReferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eAppendix UNIFIED AROMATICITY INDICES (IA) OF BIRD.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003eINDEX.\u003c\/b\u003e\u003c\/p\u003e","brand":"John Wiley \u0026 Sons Inc","offers":[{"title":"Default Title","offer_id":49402366558551,"sku":"9780470566695","price":77.36,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0817\/1739\/5799\/files\/9780470566695.jpg?v=1730480184","url":"https:\/\/bookcurl.com\/products\/fundamentals-of-heterocyclic-chemistry-9780470566695","provider":"Book Curl","version":"1.0","type":"link"}