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Niementowski quinoline synthesis

About: Niementowski quinoline synthesis is a research topic. Over the lifetime, 4 publications have been published within this topic receiving 214 citations.

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01 Jan 2009
TL;DR: Three and four-and five-members of a three-and-four-maineed HetEys were involved in the development of Aziridines and Epoxides as mentioned in this paper.
Abstract: Foreword Preface Contributing Authors PART 1 THREE- AND FOUR-MEMBERED HETEROCYCLES Chapter 1 Aziridines and Epoxides 11 Blum Aziridine Synthesis 12 Gabriel Heine Aziridine Isomerization 13 Shi Epoxidation PART 2 FIVE-MEMBERED HETEROCYCLES Chapter 2 Pyrroles and Pyrrolidines 21 Clauson Kass Pyrrole Synthesis 22 Houben Hoech Acylation of Pyrroles 23 Overman Pyrrolidine Synthesis 24 Trofimov Synthesis of Pyrroles Chapter 3 Indoles 31 Bischler Mohlau Indole Synthesis 32 Borsche Drechsel Cyclization 33 Buchwald Hartwig Indole Synthesis 34 Cadogan Sundberg Indole Synthesis 35 Fukuyama Indole Synthesis 36 Gassman Oxindole Synthesis 37 Larock Indole Synthesis 38 Matinet Dioxindole Synthesis 39 Mori Ban Indole Synthesis 310 Sandmeyer Isatin Synthesis 311 Sommelet Hauser Rearrangement 312 Stolle Oxindole Synthesis Chapter 4 Furans and Oxazoles 41 Nierenstein Reaction 42 Davidson Oxazole Synthesis 43 Fischer Oxazole Synthesis 44 Japp Oxazole Synthesis 45 Schollkopf Oxazole Synthesis Chapter 5 Other Five-Membered Heterocycles 51 Bamberger Imidazole Cleavage 52 Dimroth Triazole Synthesis 53 Finnegan Tetrazole Synthesis 54 Hantsch Thiazole Synthesis 55 Huisgen Tetrazole Rearrangement 56 Knorr Pyrazole Synthesis 57 Pechmann Pyrazole Synthesis PART 3 SIX-MEMBERED HETEROCYCLES Chapter 6 Pyridines 61 Baeyer Pyridine Synthesis 62 Katrizky Reaction Chapter 7 Quinolines and Isoquinolines 71 Betti reaction 72 Bernthsen Acridine Synthesis 73 Lehmstedt Tanasescu Reaction 74 Niementowski Quinoline Synthesis 75 Povarov Reaction Chapter 8 Six-Membered Heterocycles 81 Balaban Nenitzescu Praill Reaction 82 Borsche Cinnoline Synthesis 83 Gutknecht Pyrazine Synthesis 84 Niementowski Quinazoline Synthesis 85 Pechmann Coumarin Synthesis 86 Robinson Schopf Condensation 87 Simonis Chromone Cyclization 88 Wesseley Moser Rearrangement 89 Widman Stoermer Cinnoline Synthesis 810 Wichterle Reaction Chapter 9 Miscellaneous Name Reactions 91 ANRORC Mechanism 92 Boulton Katritzky Rearrangement 93 Chichibabin Amination Reaction 94 Dimroth Rearrangement 95 Hantzsch Synthesis 96 Ortoleva King Reaction Appendices Appendix 1, Table of Contents for Volume 1: Name Reactions in Heterocyclic Chemistry Appendix 2, Table of Contents for Volume 2: Name Reactions for Functional Group Transformations Appendix 3, Table of Contents for Volume 3: Name Reactions for Homologations-I Appendix 4, Table of Contents for Volume 4: Name Reactions for Homologations-II Appendix 5, Table of Contents for Volume 5: Name Reactions for Ring Formations

191 citations

Journal ArticleDOI
TL;DR: In this article, Anthranilamides 1, A = NR2 derived from benzamides by directed ortho metalationamination, are converted into the corresponding imines 4 which upon treatment with LDA lead to substituted 4-quinolones 5 thus providing a general new quinoline synthesis.

23 citations

Journal ArticleDOI

1 citations

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Metrics
No. of papers in the topic in previous years
YearPapers
20121
20091
19871
19861