Progress in heterocyclic chemistry. Volume 29 /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Gribble, Gordon W., Joule, J. A. (John Arthur)
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Amsterdam : Elsevier, 2017.
Temas:
Heterocyclic chemistry.
Chimie des compos�es h�et�erocycliques.
SCIENCE > Chemistry > Organic.
Heterocyclic chemistry
Acceso en línea:Texto completo
Tabla de Contenidos:
  • Front Cover; PROGRESS IN HETEROCYCLIC CHEMISTRY; PROGRESS IN HETEROCYCLIC CHEMISTRY; Copyright; CONTENTS; CONTRIBUTORS; FOREWORD; EDITORIAL ADVISORY BOARD MEMBERS PROGRESS IN HETEROCYCLIC CHEMISTRY; 1
  • Recent Advances in the Synthesis of Benzimidazol-2-ones via Rearrangements; 1.1 INTRODUCTION; 1.2 REARRANGEMENT OF BENZODIAZEPINE(DI)ONES; 1.2.1 Synthesis of Benzimidazol-2-ones From Benzodiazepinones; 1.2.2 Synthesis of Benzimidazol-2-ones From 1,5-Benzodiazepin-2,4-diones; 1.3 REARRANGEMENTS OF QUINOXALINE DERIVATIVES; 1.3.1 Synthesis of Benzimidazol-2-ones From Quinoxaline N-Oxides
  • 1.6.2 Synthesis of Benzimidazol-2-ones by Hofmann Rearrangement1.6.3 Synthesis of Benzimidazol-2-ones by Schmidt Rearrangement; 1.6.4 Synthesis of Benzimidazol-2-ones by Lossen Rearrangement; 1.7 CONCLUSIONS; ACKNOWLEDGMENT; REFERENCES; 2
  • Use of Rhodium Carbenoid Intermediates for Dipolar Cycloaddition Chemistry; 2.1 INTRODUCTION; 2.2 INTRAMOLECULAR CYCLOADDITION OF CARBONYL YLIDES; 2.2.1 Intramolecular Cycloadditions of Carbocyclic Carbonyl Ylides; 2.2.2 Involvement of a Metal-Associated Dipole; 2.2.3 Catalytic Enantioselective Intramolecular Cycloaddition
  • 2.2.4 Other Methods for Generating Carbonyl Ylide Dipoles2.2.5 Application of the Method Toward the Synthesis of Complex Natural Products; 2.2.6 Synthesis of Pseudolaric Acids; 2.2.7 Synthesis of ()-Indicol; 2.2.8 Synthesis of Polygalolides A and B; 2.2.9 Synthesis of Platensimycin; 2.2.10 Synthesis of ()-Colchicine; 2.3 INTRAMOLECULAR CYCLOADDITIONS USING ISOM�UNCHNONES AS CARBONYL YLIDE DIPOLES; 2.3.1 Model Studies Employing Isom�unchnones as Carbonyl Ylide Dipoles; 2.3.2 Synthesis of the Ergot Alkaloid System; 2.4 THIOISOM�UNCHNONE CYCLOADDITIONS
  • 2.4.1 Synthesis of the Schizozygane Alkaloid Family2.4.2 Synthesis of Atorvastatin; 2.5 CONCLUSIONS; REFERENCES; 3
  • Three-Membered Ring Systems; 3.1 INTRODUCTION; 3.2 EPOXIDES; 3.2.1 Preparation of Epoxides; 3.2.2 Reactions of Epoxides; 3.3 AZIRIDINES; 3.3.1 Preparation of Aziridines; 3.3.2 Reactions of Aziridines; 3.4 AZIRINES; 3.4.1 Preparation of Azirines; 3.4.2 Reaction of Azirines; 3.5 OXAZIRIDINES; 3.5.1 Preparation of Oxaziridines; 3.5.2 Reaction of Oxaziridines; 3.6 DIAZIRINES; REFERENCES; 4
  • Four-Membered Ring Systems; 4.1 INTRODUCTION

Ejemplares similares