Progress in heterocyclic chemistry
Gribble, Gordon W.

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  • Progress in heterocyclic chemistry
  • 紀錄類型: 書目-電子資源 : Monograph/item
    正題名/作者: Progress in heterocyclic chemistry/ edited by Gordon W. Gribble, John A. Joule.
    其他作者: Gribble, Gordon W.
    出版者: Amsterdam :Elsevier, : c2015.,
    面頁冊數: 1 online resource (xv, 627 p.)
    附註: Includes index.
    內容註: Front Cover; PROGRESS IN HETEROCYCLIC CHEMISTRY; Copyright; CONTENTS; CONTRIBUTORS; FOREWORD; EDITORIAL ADVISORY BOARD MEMBERS PROGRESS IN HETEROCYCLIC CHEMISTRY; 1 -- Propargyl Vinyl Ethers as Powerful Starting Points for Heterocycle Synthesis; 1.1 INTRODUCTION; 1.2 SYNTHESIS OF FURANS AND PYRROLES VIA PROPARGYL CLAISEN REARRANGEMENT; 1.3 SYNTHESIS OF 1,3-OXAZOLIDINES VIA MICROWAVE SYNTHESIS; 1.4 SYNTHESIS OF 2H-PYRANS AND 1,2-DIHYDROPYRIDINES; 1.5 SUMMARY; REFERENCES; 2 -- Recent Progress of Phosphonium Coupling in Heterocyclic and Medicinal Chemistry; 2.1 INTRODUCTION
    內容註: 2.2 DISCOVERY OF PHOSPHONIUM COUPLING2.2.1 Phosphonium Salts; 2.2.2 Tautomerizable Heterocycles; 2.2.3 Reaction Discovery; 2.2.4 Solvent Effect and Base Effect; 2.2.5 Reaction Mechanism; 2.3 PHOSPHONIUM COUPLING FOR DIRECT AMINATION; 2.3.1 Direct Amination; 2.3.2 Recent Progress and Application; 2.4 PHOSPHONIUM COUPLING FOR DIRECT ETHERIFICATION; 2.4.1 Direct Etherification; 2.4.2 Recent Progress and Application; 2.5 PHOSPHONIUM COUPLING FOR DIRECT THIOETHERIFICATION; 2.5.1 Direct Thioetherification; 2.5.2 Recent Progress and Application
    內容註: 2.6 PHOSPHONIUM COUPLING FOR DIRECT ALKYLATION2.6.1 Direct Alkylation; 2.6.2 Recent Progress and Application; 2.7 PHOSPHONIUM COUPLING FOR DIRECT ARYLATION; 2.7.1 Direct Arylation; 2.7.2 Reaction Mechanism; 2.7.3 Recent Progress and Application; 2.8 PHOSPHONIUM COUPLING FOR DIRECT ALKYNYLATION; 2.8.1 Direct Alkynylation; 2.8.2 Reaction Mechanism; 2.8.3 Recent Progress and Application; 2.9 PHOSPHONIUM COUPLING FOR NUCLEOSIDE CHEMISTRY; 2.9.1 Multistep Transformation; 2.9.2 Single Step Transformation; 2.10 SUMMARY; REFERENCES; 3 -- Three-Membered Ring Systems; 3.1 INTRODUCTION
    內容註: 3.2 EPOXIDES3.2.1 Preparation of Epoxides; 3.2.2 Reactions of Epoxides; 3.3 AZIRIDINES; 3.3.1 Preparation of Aziridines; 3.3.2 Reactions of Aziridines; REFERENCES; 4 -- Four-Membered Ring Systems; 4.1 INTRODUCTION; 4.2 AZETIDINES, AZETINES, AND RELATED SYSTEMS; 4.3 MONOCYCLIC 2-AZETIDINONES (Β-LACTAMS); 4.4 FUSED AND SPIROCYCLIC Β-LACTAMS; 4.5 OXETANES, DIOXETANES, AND 2-OXETANONES (Β-LACTONES); 4.6 THIETANES AND RELATED SYSTEMS; 4.7 SILICON AND PHOSPHORUS HETEROCYCLES: MISCELLANEOUS; REFERENCES; 5.1 -- Five-Membered Ring Systems: Thiophenes and Se/Te Derivatives
    內容註: 5.1.1 INTRODUCTION5.1.2 SYNTHESIS OF THIOPHENES, SELENOPHENES, AND TELLUROPHENES; 5.1.3 ELABORATION OF THIOPHENES AND BENZOTHIOPHENES; 5.1.4 SYNTHESIS OF THIOPHENES, SELENOPHENES, AND TELLUROPHENES FOR THE USE IN THE MATERIAL SCIENCES; 5.1.5 THIOPHENE, SELENOPHENE, AND TELLUROPHENE DERIVATIVES IN MEDICINAL AND ENVIRONMENTAL CHEMISTRY; REFERENCES; 5.2 -- Five-Membered Ring Systems: Pyrroles and Benzo Analogs; 5.2.1 INTRODUCTION; 5.2.2 SYNTHESIS OF PYRROLES; 5.2.2.1 Intramolecular Approaches to Pyrroles; 5.2.2.1.1 Intramolecular Type a; 5.2.2.1.2 Intramolecular Type c
    標題: Heterocyclic chemistry. -
    電子資源: http://www.sciencedirect.com/science/book/9780081000243click for full text
    ISBN: 0081000472 (electronic bk.)
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