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1. |
Record Nr. |
UNINA9910784864003321 |
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Autore |
Fraser T. G. |
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Titolo |
Ireland in conflict, 1922-1998 / / T.G. Fraser |
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Pubbl/distr/stampa |
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London ; ; New York : , : Routledge, , 2000 |
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ISBN |
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1-134-70857-2 |
1-134-70858-0 |
1-280-14928-0 |
9786610149285 |
0-203-97942-7 |
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Descrizione fisica |
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1 online resource (104 p.) |
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Collana |
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Disciplina |
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Soggetti |
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Political violence - Ulster (Northern Ireland and Ireland) - History - 20th century |
Social conflict - Ulster (Northern Ireland and Ireland) - History - 20th century |
Ireland History 1922- |
Northern Ireland History |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Note generali |
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Description based upon print version of record. |
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Nota di bibliografia |
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Includes bibliographical references. |
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Nota di contenuto |
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Cover; Ireland in Conflict 1922-1998; Copyright; Contents; Preface; Chronological table; 1 Settlement and civil war; 2 Political and economic evolution: North and South; 3 From de Valera to the Republic; 4 Post-war Ireland; 5 O'Neill and the rise of the civil rights campaign; 6 The Troubles begin; 7 Northern Ireland in crisis; 8 From the Anglo-Irish Agreement to the Good Friday Agreement; 9 Reflections and conclusion; Further reading |
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Sommario/riassunto |
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Ireland in Conflict, 1922-1998 sets out the main political, economic and social developments in Ireland, north and south of the border, since the 1922 treaty.This book explains the troubles in their context and examines the underlying tensions which led to prolonged violence after a period of relative civil peace and rising prosperity.Ireland in Conflict discusses:* the Civil War, its legacy for Irish politics and the Boundary Commission* the IRA, Orange Order and the Unionist party* the role of the Catholic Church and the Protestant minority<B |
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2. |
Record Nr. |
UNINA9910410048603321 |
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Autore |
Knittl-Frank Christian |
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Titolo |
A Concise Semisynthesis of Hederagonic Acid : C–H Activation in Natural Product Synthesis / / by Christian Knittl-Frank |
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Pubbl/distr/stampa |
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Wiesbaden : , : Springer Fachmedien Wiesbaden : , : Imprint : Springer Spektrum, , 2020 |
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ISBN |
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Edizione |
[1st ed. 2020.] |
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Descrizione fisica |
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1 online resource (XIX, 60 p. 1 illus.) |
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Collana |
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Disciplina |
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Soggetti |
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Catalysis |
Chemistry |
Bioorganic chemistry |
Chemical Synthesis |
Bioorganic Chemistry |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Nota di contenuto |
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Hederagonic Acid and C−H Activation; Optimization of the Synthetic Sequence -- Final Synthetic Route to Hederagonic Acid -- Experimental Section. |
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Sommario/riassunto |
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Christian Knittl-Frank reports on the development of a novel synthetic route to the naturally occurring polyhydroxylated oleanane, hederagonic acid. Polyhydroxylated oleananes are a vast family of naturally occurring triterpenoids with versatile biological activities. A low commercial availability combined with high prices make these molecules interesting targets in natural product synthesis. The developed synthetic approach starts from oleanolic acid, a cheap material that is commercially available in bulk quantities. It features several multi-step one-pot reactions, allowing a minimization of the number of steps and reducing the preparative effort. Importantly, catalytic C–H functionalization was achieved at unusually low temperatures. Hederagonic acid was thus prepared in as little as four steps, resulting in the shortest semisynthesis of this oleanane to date. Contents Hederagonic Acid and C−H Activation; Optimization of the Synthetic Sequence Final Synthetic Route to Hederagonic Acid |
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Experimental Section Target Groups Scientists and students in the field of organic chemistry, especially natural product synthesis The Author Christian Knittl-Frank is currently pursuing his PhD studies, focusing on natural product synthesis and synthetic methodology, at the Department of Organic Chemistry, University of Vienna, Austria. He is part of the MolTag doctoral program that aims to development new molecular drugs targeting ion channels. . |
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