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Heterocyclic Chemistry in Drug Discovery

Detalles Bibliográficos
Autor principal: Li, Jie Jack
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Newark : John Wiley & Sons, Incorporated, 2013.
Colección:New York Academy of Sciences Ser.
Temas:
Acceso en línea:Texto completo

MARC

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035 |a (OCoLC)1347028178 
082 0 4 |a 615.1/9  |q OCoLC  |2 23/eng/20230216 
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100 1 |a Li, Jie Jack. 
245 1 0 |a Heterocyclic Chemistry in Drug Discovery  |h [electronic resource]. 
260 |a Newark :  |b John Wiley & Sons, Incorporated,  |c 2013. 
300 |a 1 online resource (722 p.). 
490 1 |a New York Academy of Sciences Ser. 
500 |a Description based upon print version of record. 
505 0 |a Cover -- Title Page -- Copyright Page -- Contents -- Preface -- Contributing Authors -- Chapter 1 Introduction -- 1.1 Nomenclature of Heterocycles -- 1.2 Aromaticity of Heterocycles -- 1.3 Importance of Heterocycles in Life -- 1.4 Importance of Heterocycles in Drug Discovery -- 1.4.1 Five-Membered Heterocycles with One Heteroatom -- 1.4.2 Five-Membered Heterocycles with Two Heteroatoms -- 1.4.3 Six-Membered Heterocycles with One Heteroatom -- 1.4.4 Six-Membered Heterocycles with Two Heteroatoms -- PART I FIVE-MEMBERED HETEROCYCLES WITH ONE HETEROATOM -- Chapter 2 Pyrroles -- 2.1 Introduction 
505 8 |a 2.2 Reactivity of the Pyrrole Ring -- 2.2.1 Protonation -- 2.2.2 C2 Electrophilic Substitution -- 2.2.3 C3 Electrophilic Substitution -- 2.2.4 Metalation -- 2.3 Construction of the Pyrrole Rings -- 2.3.1 Knorr Pyrrole Synthesis -- 2.3.2 Paal-Knorr Pyrrole Synthesis -- 2.3.3 Hantsch Pyrrole Synthesis -- 2.3.4 Barton-Zard Reaction -- 2.4 Palladium Chemistry of Pyrroles -- 2.5 Possible Liabilities of Pyrrole-Containing Drugs -- 2.6 Problems -- 2.7 References -- Chapter 3 Indoles -- 3.1 Introduction -- 3.2 Reactivity of the Indole Ring -- 3.2.1 Protonation -- 3.2.2 C3 Electrophilic Substitution 
505 8 |a 3.2.3 C2 Electrophilic Substitution -- 3.2.4 Metallation -- 3.3 Construction of the Indole Rings -- 3.3.1 Fischer Indole Synthesis -- 3.3.2 Mori-Ban Indole Synthesis -- 3.3.3 Larock Indole Synthesis -- 3.3.4 Bischler-Möhlau Indole Synthesis -- 3.3.5 Nenitzescu Indole Synthesis -- 3.3.6 Bartoli Indole Synthesis -- 3.3.7 Batcho-Leimgruber Indole Synthesis -- 3.3.8 Gassman Indole Synthesis -- 3.3.9 Cadogan-Sundberg Indole Synthesis -- 3.4 Oxindole-containing Drug Synthesis -- 3.5 Cross-coupling Reactions for Indoles -- 3.5.1 Palladium-Catalyzed Oxidative Coupling -- 3.5.2 Negishi Coupling 
505 8 |a 3.5.3 Suzuki Coupling -- 3.5.4 Sonogashira Coupling -- 3.5.5 Heck Reaction -- 3.6 Azaindoles -- 3.6.1 Larock Reaction -- 3.6.2 Bartoli Reaction -- 3.6.3 Batcho-Leimgruber Reaction -- 3.6.4 Cadogan-Sundberg Indole Synthesis -- 3.7 Possible Liabilities of Drugs Containing 3-Methylindole -- 3.8 Problems -- 3.9 References -- Chapter 4 Furans, Benzofurans, Thiophenes, and Benzothiophenes -- 4.1 Introduction -- 4.2 Furans and Benzofurans -- 4.2.1 Reactions of Furans and Benzofurans -- 4.2.2 Furan and Benzofuran Synthesis -- 4.2.3 Synthesis of Furan- and Benzofuran-Containing Drugs 
505 8 |a 4.3 Thiophenes and Benzothiophenes -- 4.3.1 Reactions of Thiophene and Benzothiophene -- 4.3.2 Synthesis of Thiophene and Benzothiophene -- 4.3.3 Synthesis of Thiophene- and Benzothiophene-Containing Drugs -- 4.4 Possible Liabilities of Furan- and Thiophene-Containing Drugs -- 4.5 Problems -- 4.6 References -- PART II FIVE-MEMBERED HETEROCYCLES WITH TWO OR MORE HETEROATOMS -- Chapter 5 Pyrazoles, Pyrazolones, and Indazoles -- 5.1 Introduction -- 5.1.1 Basicity and Acidity -- 5.1.2 Tautomerization -- 5.2 Reactivities of the Pyrazole Ring -- 5.2.1 Alkylation of the Pyrazole Ring 
500 |a 5.2.2 C4 Electrophilic Substitution 
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776 0 8 |i Print version:  |a Li, Jie Jack  |t Heterocyclic Chemistry in Drug Discovery  |d Newark : John Wiley & Sons, Incorporated,c2013  |z 9781118148907 
830 0 |a New York Academy of Sciences Ser. 
856 4 0 |u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=7103576  |z Texto completo 
938 |a ProQuest Ebook Central  |b EBLB  |n EBL7103576 
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