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Progress in heterocyclic chemistry[electronic resource] /

紀錄類型:	書目-電子資源 : Monograph/item
杜威分類號:	547.5/9/05
書名/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.
標題:	Heterocyclic chemistry.
標題:	Heterocyclic compounds - Indexes.
ISBN:	0081000472 (electronic bk.)
ISBN:	9780081000472 (electronic bk.)
ISBN:	0081000243 (electronic bk.)
ISBN:	9780081000243 (electronic bk.)
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
電子資源:	click for full text

Progress in heterocyclic chemistry[electronic resource] /
Progress in heterocyclic chemistry[electronic resource] /edited by Gordon W. Gribble, John A. Joule. - Amsterdam :Elsevier,c2015. - 1 online resource (xv, 627 p.) - Progress in Heterocyclic Chemistry..

Includes index.

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

ISBN: 0081000472 (electronic bk.)Subjects--Topical Terms:

444168
Heterocyclic chemistry.

LC Class. No.: QD399

Dewey Class. No.: 547.5/9/05

Progress in heterocyclic chemistry[electronic resource] /
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245 0 0 $a Progress in heterocyclic chemistry $h [electronic resource] / $c edited by Gordon W. Gribble, John A. Joule.
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505 0 $a 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
505 8 $a 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
505 8 $a 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
505 8 $a 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
505 8 $a 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
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700 1 $a Joule, J. A. $q (John Arthur) $3 486523
830 0 $a Progress in Heterocyclic Chemistry. $3 658878
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