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170907s2017 ne o 001 0 eng d |
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|a 1002847896
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|a 9780081023112
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|a 0081023111
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|z 9780081023105
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|a Progress in heterocyclic chemistry.
|b Volume 29 /
|c edited by Gordon W. Gribble, John A. Joule.
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| 260 |
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|a Amsterdam :
|b Elsevier,
|c 2017.
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| 300 |
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|a 1 online resource
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| 336 |
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|a text
|b txt
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|a computer
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|a 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
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| 505 |
8 |
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|a 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
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|a 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
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| 505 |
8 |
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|a 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
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| 500 |
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|a Includes index.
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| 588 |
0 |
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|a Print version record.
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| 650 |
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0 |
|a Heterocyclic chemistry.
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| 650 |
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6 |
|a Chimie des compos�es h�et�erocycliques.
|0 (CaQQLa)201-0308175
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| 650 |
|
7 |
|a SCIENCE
|x Chemistry
|x Organic.
|2 bisacsh
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| 650 |
|
7 |
|a Heterocyclic chemistry
|2 fast
|0 (OCoLC)fst00955735
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| 700 |
1 |
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|a Gribble, Gordon W.
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| 700 |
1 |
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|a Joule, J. A.
|q (John Arthur)
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| 776 |
0 |
8 |
|i Print version:
|t Progress in heterocyclic chemistry.
|d Amsterdam : Elsevier, 2017
|z 0081023103
|z 9780081023105
|w (OCoLC)975018918
|
| 856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/bookseries/09596380/29
|z Texto completo
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| 880 |
8 |
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|6 505-00/(N
|a 1.3.2 Synthesis of Benzimidazol-2-ones From Quinoxalin-2(1Н)-Ones1.4 REARRANGEMENT OF TETRAZOLONES; 1.5 REARRANGEMENTS OF CONDENSED AND SPIRO COMPOUNDS WITH A BENZIMIDAZOLE SYSTEM; 1.5.1 Synthesis of Benzimidazol-2-ones From Thiazolo[1,2-a]benzimidazolium Salts; 1.5.2 Synthesis of Benzimidazol-2-ones From Hydroxybenzimidazol[2,1-b]thiazanium Salts; 1.5.3 Synthesis of Benzimidazol-2-ones From Spiro-benzimidazolines; 1.6 REARRANGEMENTS OF ANTHRANILIC ACID AND ITS DERIVATIVES; 1.6.1 Synthesis of Benzimidazol-2-ones by Curtius Rearrangement
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