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Record Nr. |
UNINA9910452276803321 |
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Autore |
Apple Michael W. |
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Titolo |
Knowledge, power, and education : the selected works of Michael W. Apple / / Michael W. Apple |
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Pubbl/distr/stampa |
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New York, N.Y. ; ; London : , : Routledge, , 2013 |
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ISBN |
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0-203-11811-1 |
1-283-89403-3 |
1-136-30782-6 |
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Descrizione fisica |
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1 online resource (297 p.) |
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Collana |
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World library of educationalists series |
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Disciplina |
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Soggetti |
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Critical pedagogy |
Educational sociology |
Education and state |
Education - Curricula |
Electronic books. |
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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 and index. |
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Nota di contenuto |
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Front Cover; Knowledge, Power, and Education; Copyright Page; Contents; Acknowledgments; 1 On Being a Scholar/Activist: An Introduction to Knowledge, Power, and Education; 2 On Analyzing Hegemony; 3 Commonsense Categories and the Politics of Labeling; 4 Seeing Education Relationally: The Stratification of Culture and People in the Sociology of School Knowledge (with Lois Weis); 5 Curricular Form and the Logic of Technical Control: Commodification Returns; 6 Controlling the Work of Teachers; 7 The Other Side of the Hidden Curriculum: Culture as Lived-I |
8 The Culture and Commerce of the Textbook9 Cultural Politics and the Text; 10 Consuming the Other: Whiteness, Education, and Cheap French Fries; 11 The Politics of Official Knowledge: Does a National Curriculum Make Sense?; 12 Producing Inequalities: Conservative Modernization in Policy and Practice; 13 "We Are the New Oppressed": Gender, Culture, and the Work of Home Schooling; 14 Global Crises, Social Justice, and Teacher Education; About the Author; Index |
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Sommario/riassunto |
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"For more than three decades, Michael W. Apple has sought to uncover |
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and articulate the connections among knowledge, teaching, and power in education. His germinal Ideology and curriculum was a watershed title in critical education studies, and has remained in print since its publication in 1979. The more than two dozen books and hundreds of papers, articles, and chapters published since have likewise all contributed to a greater understanding of the relationship between and among the economy, political, and cultural power in society on the one hand "and the ways in which education is thought about, organized, and evaluated" on the other. In this collection, Apple brings together 13 of his key writings in one place, providing an overview not just of his own career, but of the larger development of the field. A new introduction re-examines the scope of his work and his earlier arguments, and reflects on what remains to be done for those committed to critical education"-- |
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2. |
Record Nr. |
UNINA9911019440203321 |
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Titolo |
Asymmetric synthesis with chemical and biological methods / / edited by Dieter Enders and Karl-Erich Jaeger |
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Pubbl/distr/stampa |
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Weinheim, : Wiley-VCH |
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Chichester, : John Wiley [distributor], 2007 |
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ISBN |
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9786610921584 |
9781280921582 |
1280921587 |
9783527610648 |
3527610642 |
9783527610631 |
3527610634 |
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Descrizione fisica |
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1 online resource (472 p.) |
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Altri autori (Persone) |
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EndersDieter |
JaegerKarl-Erich |
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Disciplina |
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Soggetti |
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Asymmetric synthesis |
Organic compounds - Synthesis |
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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 and index. |
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Nota di contenuto |
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Asymmetric Synthesis with Chemical and Biological Methods; Foreword; Contents; Preface; List of Contributors; 1 Stoichiometric Asymmetric Synthesis; 1.1 Development of Novel Enantioselective Synthetic Methods; 1.1.1 Introduction; 1.1.2 α-Silyl Ketone-Controlled Asymmetric Syntheses; 1.1.2.1 Regio- and Enantioselective α-Fluorination of Ketones; 1.1.2.2 α-Silyl Controlled Asymmetric Mannich Reactions; 1.1.3 Asymmetric Hetero-Michael Additions; 1.1.3.1 Asymmetric Aza-Michael Additions; 1.1.3.2 Asymmetric Oxa-Michael Additions; 1.1.3.3 Asymmetric Phospha-Michael Additions |
1.1.4 Asymmetric Syntheses with Lithiated α-Aminonitriles1.1.4.1 Asymmetric Nucleophilic α-Aminoacylation; 1.1.4.2 Asymmetric Nucleophilic Alkenoylation of Aldehydes; 1.1.5 Asymmetric Electrophilic α-Substitution of Lactones and Lactams; 1.1.6 Asymmetric Synthesis of α-Phosphino Ketones and 2-Phosphino Alcohols; 1.1.7 Asymmetric Synthesis of 1,3-Diols and anti-1,3-Polyols; 1.1.8 Asymmetric Synthesis of α-Substituted Sulfonamides and Sulfonates; 1.2 Asymmetric Synthesis of Natural Products Employing the SAMP/RAMP Hydrazone Methodology; 1.2.1 Introduction; 1.2.2 Stigmatellin A |
1.2.3 Callistatin A1.2.4 Dehydroiridodiol(dial) and Neonepetalactone; 1.2.5 First Enantioselective Synthesis of Dendrobatid Alkaloids Indolizidine 209I and 223J; 1.2.6 Efficient Synthesis of (2S,12 ́R)-2-(12 ́-Aminotridecyl)pyrrolidine, a Defense Alkaloid of the Mexican Bean Beetle; 1.2.7 2-epi-Deoxoprosopinine; 1.2.8 Attenol A and B; 1.2.9 Asymmetric Synthesis of (+)- and (-)-Streptenol A; 1.2.10 Sordidin; 1.2.11 Prelactone B and V; 1.3 Asymmetric Synthesis Based on Sulfonimidoyl-Substituted Allyltitanium Complexes; 1.3.1 Introduction |
1.3.2 Hydroxyalkylation of Sulfonimidoyl-Substituted Allylltitanium Complexes1.3.2.1 Sulfonimidoyl-Substituted Bis(allyl)titanium Complexes; 1.3.2.2 Sulfonimidoyl-Substituted Mono(allyl)tris(diethylamino)titanium Complexes; 1.3.3 Aminoalkylation of Sulfonimidoyl-Substituted Allyltitanium Complexes; 1.3.3.1 Sulfonimidoyl-Substituted Bis(allyl)titanium Complexes; 1.3.3.2 Sulfonimidoyl-Substituted Mono(allyl)tris(diethylamino)titanium Complexes; 1.3.4 Structure and Reactivity of Sulfonimidoyl-Substituted Allyltitanium Complexes; 1.3.4.1 Sulfonimidoyl-Substituted Bis(allyl)titanium Complexes |
1.3.4.2 Sulfonimidoyl-Substituted Mono(allyl)titanium Complexes1.3.5 Asymmetric Synthesis of Homopropargyl Alcohols; 1.3.6 Asymmetric Synthesis of 2,3-Dihydrofurans; 1.3.7 Synthesis of Bicyclic Unsaturated Tetrahydrofurans; 1.3.8 Asymmetric Synthesis of Alkenyloxiranes; 1.3.9 Asymmetric Synthesis of Unsaturated Mono- and Bicyclic Prolines; 1.3.10 Asymmetric Synthesis of Bicyclic Amino Acids; 1.3.11 Asymmetric Synthesis of β-Amino Acids; 1.3.12 Conclusion; 1.4 The "Daniphos" Ligands: Synthesis and Catalytic Applications; 1.4.1 Introduction; 1.4.2 General Synthesis |
1.4.3 Applications in Stereoselective Catalysis |
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Sommario/riassunto |
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Edited by two of the leading researchers in the field, this book provides a deep, interdisciplinary insight into stoichiometric and catalytic reactions in this continuously expanding area. A plethora of top German scientists with an international reputation covers various aspects, from classical organic chemistry to process development, and from the theoretical background to biological methods using enzymes. Throughout the focus is on the development of new synthetic methods in asymmetric synthesis, the synthesis of natural and bioactive compounds and the latest developments in both chemical a |
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