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  • 1
    Online Resource
    Online Resource
    New York :Cambridge University Press,
    Keywords: Disaster relief. ; Electronic books.
    Description / Table of Contents: Presents eighteen case studies of natural disasters from around the world. By comparing the impacts, it aims to inform actual adaptation practice - what works, what does not, and why. Especially useful for researchers and decision makers in policy and government concerned with climate change, disaster management and environmental policy.
    Type of Medium: Online Resource
    Pages: 1 online resource (290 pages)
    Edition: 1st ed.
    ISBN: 9781107503472
    DDC: 363.738747
    Language: English
    Note: Intro -- Contents -- Contributors -- Preface -- 1 Introduction -- 1.1 The Rationale for This Book -- 1.2 The Structure of This Book -- 2 Climate Change and Disaster Risk Management: Challenges and Opportunities -- 2.1 Challenges of Climate Change and Disaster Risk: Space and Time Scales -- 2.2 Knowledge for Action -- 2.3 Changing Policies and Practices That Can Make a Difference on the Ground -- 2.4 Conclusion -- Acknowledgements -- Part I Case Studies from North America -- A Few Words on Andrew W. Garcia -- 3 Hurricane Katrina and the City of New Orleans -- 3.1 Katrina Meteorology -- 3.2 Katrina Surge Effects -- 3.3 The Hurricane Protection System -- 3.4 The Consequences -- 3.5 Findings and Lessons Learned -- 3.6 Societal Effects -- 3.7 Concluding Remarks -- 4 A Brief History of Flooding and Flood Control Measures Along the Mississippi River Basin -- 4.1 History of Levee Building and Floods on the Mississippi River -- Acknowledgments -- 5 The 2003 and 2007 Wildfires in Southern California -- 5.1 Prior Condition -- 5.2 Vulnerability -- 5.3 Resilience -- 5.4 Physical Characteristics of the Event -- 5.5 Emergency Management -- 5.6 Post-Event Adaptation -- 5.7 Climate Change Impacts on Southern California Fire Regimes -- 5.8 What Are the Lessons Learned? -- 6 Adapting to Extreme Heat Events: Thirty Years of Lessons Learned from the Kansas City, Missouri, Extreme Heat Program -- 6.1 July 1980 EHE in Kansas City -- 6.2 Kansas City's EHP -- 6.3 Lessons Learned for Climate Change Adaptation Efforts -- Reinforce vs. Reinvent Responses -- Place the Future in the Appropriate Context -- Always Try to Improve Public Education, but Be Ready to Act -- There Are Many Useful Tools, but No One Tool -- Partnerships Enhance Adaptation Opportunities -- 6.4 Conclusions -- Part II Case Studies from Australia. , 7 Drought and Water in the Murray-Darling basin: From Disaster Policy to Adaptation -- 7.1 Drought Policy Pre-1989 -- 7.2 The Policy Transition -- 7.3 Drought and Water Allocation -- 7.4 Lessons for Adaptation -- 8 After 'Black Saturday': Adapting to Bushfires in a Changing Climate -- 8.1 Environmental Factors -- Maximum Temperature -- Drought Factor -- Relative Humidity -- Wind Speed -- 8.2 Human Factors -- 8.3 Changes to Bushfire Policy and Management -- 8.4 Adapting to Bushfires in a Changing Climate -- 9 Cyclone Tracy and the Road to Improving Wind-Resistant Design -- 9.1 Cyclone Tracy -- 9.2 Extent and Causes of Damage -- 9.3 Adaptation of Building Design and Regulation -- 9.4 Lessons -- The Role of Scientific Input -- The Role of Regulation and Building Codes -- Opportunities and Conditions for Adaptation -- Inclusion and Education -- 9.5 Conclusions -- 10 Adaptation and Resilience in Two Flood-Prone Queensland Communities -- 10.1 The 2008 Floods in Charleville and Mackay -- Charleville -- Mackay -- 10.2 Impacts of the 2008 Floods -- Charleville -- Mackay -- 10.3 Recognising Vulnerability -- 10.4 Building Resilience and Mitigation -- 10.5 Strategies for Adaptive Capacity and Community Viability -- 10.6 Conclusion: Policy, Legislation and Community Adaptation Strategies -- Part III Case Studies from Europe -- 11 Windstorms, the Most Costly Natural Hazard in Europe -- 11.1 The Role of Windstorms in Europe -- 11.2 Identification of Windstorms -- 11.3 Physical Processes Leading to Windstorms -- Recent Variability of Windstorms and Their Impacts -- 11.4 Scenarios of Future Windstorms and Their Impacts -- 11.5 Adaptation -- 12 The 2003 Heatwave: Impacts, Public Health Adaptation and Response in France -- 12.1 Meteorological Characteristics of the 2003 Heatwave -- 12.2 The Burden of the 2003 Heatwave -- 12.3 The First Signals and the Initial Response. , 12.4 The National Prevention Plan -- 12.5 Conclusions -- 13 Lessons from River Floods in Central Europe, 1997-2010 -- 13.1 Context -- 13.2 Floods in Central Europe in Perspective -- Floods of 1997 -- Floods of 2002 -- Floods of 2010 -- 13.3 Change Detection and Attribution -- 13.4 Flood Management and Flood Risk Management -- 13.5 Concluding Remarks -- 14 Lessons Learned from the North Sea Flooding Disaster in the Netherlands, 1953 -- 14.1 What Happened? -- 14.2 Really a Surprise? -- 14.3 Vulnerability and Responsibility -- 14.4 Major Investments after the Event: The Delta Plan -- 14.5 Evaluation of the Delta Plan -- 14.6 Climate Change and Sea Level Rise -- 14.7 Flooding Disasters: A Historic Necessity for Improvements in Flood Protection? -- Part IV Case Studies from the Developing World -- 15 Adapting to Drought in the West African Sahel -- 15.1 The Sahel - Physical Characteristics and Drought -- 15.2 Responses to Drought in Northern Nigeria in the 1970s -- 15.3 From Coping to Adaptation Strategies -- 15.4 Productive Bricolage -- 15.5 Climate and Development Aid -- 15.6 Conclusion -- Acknowledgements -- 16 The 2004 Indian Ocean Tsunami: Sri Lankan Experience -- 16.1 The Event -- 16.2 The Impacts -- 16.3 The Aftermath -- 16.4 The Lessons -- 17 Recovery Efforts: The Case of the 2007 Cyclone Sidr in Bangladesh -- 17.1 Sidr Recovery Efforts -- 17.2 Sidr Housing Recovery Efforts -- 17.3 Conclusions -- 18 Coffee, Disasters and Social-Ecological Resilience in Guatemala and Chiapas, Mexico -- 18.1 Coffee and Disaster -- 18.2 Disaster Management and Response -- Acknowledgements -- 19 Responding to Floods in the Nile basin: A Case Study of the 1997-1998 Floods in the Upper White Nile -- 19.1 Flood Response and Adaptation to Climate Change -- 19.2 Flooding in the White Nile Around Lake Kyoga and Lake Victoria in 1997 and 1998: Impacts and Responses. , Description of the Flood Event and Its Impacts -- Vulnerability and Resilience to Flooding in Lake Shore Villages -- Responses to Flooding: Emergency Management and Post-Event Behaviour -- Present-Day Vulnerability to Floods in the White Nile Basin -- 19.3 Adaptation to Floods in Nile Basin in the Present Day: Lessons Learned -- 20 Floods in the Yangtze River Basin, China -- 20.1 Context -- 20.2 Floods on the Yangtze in the Last 150 Years -- The 1998 Floods -- The 2010 Floods -- 20.3 Climate Change Track- Observations and Projections -- 20.4 Adaptation- Lessons Learned -- 20.5 Gaps in Knowledge and Concluding Remarks -- Part V Synthesis Chapters -- 21 Disasters and Development -- 21.1 The Relationship between Development and Climate-Related Disasters -- 21.2 The Role of Development in Shaping Climate-Related Disaster Risk Reduction and Response -- 21.3 Managing Disasters in Developed and Developing Country Contexts: A Review of Case Studies -- The 'Impacts-Based' Approach to Risk Management in Developed Countries -- Disaster Risk Management in Developing Countries -- 21.4 Discussion and Conclusions -- Acknowledgements -- 22 What Next? Climate Change as a Game-Changer for Policy and Practice -- 22.1 Playing Together: Disaster Risk Reduction and Climate Change Adaptation -- 22.2 A Spectator's View -- 22.3 A Dance with Change -- 22.4 Conclusions -- 23 Barriers and Limits to Adaptation: Cautionary Notes -- 23.1 Barriers, Limits and Maladaptation in Theory -- Barriers to Adaptation -- Limits to Adaptation -- Maladaptation -- 23.2 Barriers, Limits and Maladaptation in Practice -- Barriers to Adaptation -- Limits to Adaptation -- Maladaptation -- 23.3 Conclusions -- 24 Lessons Learned for Adaptation to Climate Change -- 24.1 The Events (and Before) -- 24.2 Vulnerability and Resilience -- 24.3 Adaptation Actions Following the Event -- Immediate Responses. , Long-Term Responses -- 24.4 Reflections on Historical Adaptation to Climate (as Different from Future Planning for Climate Change) -- Recognising Change - Disaster Versus Variability -- Where Does Risk Lie? - Avoiding 'Maladaptation' -- Acceptable Risk and the Associated Costs -- 24.5 The Future Impact of Climate Change on Disaster Management -- 24.6 Lessons Learned -- Community Awareness -- The Whole Picture: All Hazards -- Enabling Adaptation -- Practicality -- Final Reflections -- Adaptation in a Changing Climate -- 25 Afterword: Floods, Storms, Fire and Pestilence - Disaster Risk in Australia During 2010-2011 -- 25.1 Disasters and Response - Australia in 2010/2011 -- 25.1.1 Locust Plague -- 25.1.2 Floods -- Recovery -- Rebuilding and Adapting -- 25.1.3 Cyclone Yasi -- 25.1.4 Heatwaves and Fire -- 25.2 The National Scale -- National Emergency Management Planning -- 25.3 The Role of Climate -- 25.4 Conclusion -- Index.
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  • 2
    Online Resource
    Online Resource
    Seattle :University of Washington Press,
    Keywords: Europeans - Travel - India - History - 19th century. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (314 pages)
    Edition: 1st ed.
    ISBN: 9780295800943
    Series Statement: Culture, Place, and Nature Series
    DDC: 304.2/0954/09034
    Language: English
    Note: Intro -- Contents -- Acknowledgments -- Introduction -- 1. Itinerant Empire -- 2. In a Land of Death -- 3. Romanticism and Improvement -- 4. From the Orient to the Tropics -- 5. Networks and Knowledges -- 6. Botany and the Bounds of Empire -- Conclusion -- Notes -- Bibliography -- Index.
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  • 3
    Online Resource
    Online Resource
    Chicago :Austin Macauley Publishers,
    Keywords: Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (191 pages)
    ISBN: 9781398426894
    Language: English
    Note: Intro -- The Matrix of the Mind -- About the Author -- Dedication -- Copyright Information © -- Preface -- Chapter 1 In the Beginning -- the Start of the Cosmos -- Critical Rate of Expansion -- Fundamental Numbers -- The Laws of Science -- Strange Denizens of the Universe -- The Solar System -- Formation of Planet Earth and the Moon -- Chapter 2 Making the Impossible Happen -- The Statistics -- Proteins -- One of the Building Blocks of Life -- Did Life Arise by Random Chance Alone? -- The Left-Hand Right-Hand Problem -- The First Life Form -- The Miller-Urey Experiment -- How Can Life Arise from Lifeless Matter? -- The Essential Properties of Water -- The Unique Properties of the Carbon Atom -- The Importance of The Earth's Magnetic Field -- The Atmosphere -- The Carbon Dioxide (CO2) Cycle -- Chapter 3 Domains of the Conscious and Unconscious -- an Overview -- A Brief Review -- An Introduction to the Personal Unconscious -- An Introduction to the Collective Unconscious -- Expanding the Definitions to the Domains of the Intelligent Universe -- The Universal Unconscious and the Intelligent Universe -- The Primary Formative Unconscious (PFU) Family -- Consciousness in Humans -- The Psi-Domain -- The Wider Primary Formative Unconscious Family -- The Species Formative Unconscious (SFU) -- The Hierarchical Family of the Domains of the Unconscious -- The Species Group Unconscious (SGU) -- The Species Individual Unconscious (SIU) -- More on the Collective Unconscious -- A Brief Description of a Few Archetypes -- The Duad -- Chapter 4 The Effectuators -- The Function of the Effectuators -- First Effectuator: The Primary Formative Unconscious Family (PFU) -- The SFU Family Evolved Establishing Later Life Forms. -- The Amazing Navigational Capability of the Eel. -- The Flatid Bug -- The Astounding Formation Flying of the Starling -- The Turtle Arribada. , Migrating Birds -- An Experiment with Termites -- Bees and Their Hives -- The Social Order of Ants -- The Second Effectuator: The Laws of Science -- Third Effectuator: The Sun -- Fourth Effectuator: The Earth -- Fifth Effectuator: The Moon -- Sixth Effectuator: The Planets -- Seventh Effectuator: Evolution -- Eighth Effectuator: Mutation -- Chapter 5 Life Within the Intelligent Universe -- Defining Life -- Efficient Replication -- The Establishment of Self-Organising and Self-Regulating Systems -- Daisyworld -- an Example of Environmental Self-Regulation -- The Mysteries of Coding: The Transfer of Information -- The Bacteria Ideation -- Reactive Behaviour -- The Bacterial Contribution to the Formation of the Atmosphere -- The Ocean Environment -- Nucleated Cells -- The Limitations of DNA -- Stem Cells -- The Homeobox Gene -- The Genome Project -- Chapter 6 Evolution and Diversification of Life -- The Evolution of Species -- The Rise of Humankind: Homo Sapiens -- Chapter 7 The Matrix Model -- Overview -- The Matrix Model for Humankind -- The Environment -- The Physical Body -- The Human Brain Duad -- Memory -- Acquired Characteristics -- McDougall's Experiment with Rats -- The Lower Conscious -- The Higher Conscious -- The Species Individual Unconscious (SIU) in the Matrix Model -- The Species Group Unconscious (SGU) in the Matrix Model -- The Species Formative Unconscious (SFU) in the Matrix Model -- The Primary Formative Unconscious (PFU) in the Matrix Model -- The Universal Unconscious (UU) in the Matrix Model -- The Mind and the Matrix Model for Mankind -- The Mind Domains of the Matrix Model for Mankind -- The Relationship Between Zones of The Mind -- The Monad -- Thought Monads -- The Matrix Model and Life After Death. -- Traditions Relating to the Empowerment of Material Objects and Places of Power -- Chapter 8 The Para-Normal. , A Problem Field for Researchers -- Noetic Science -- Telepathy -- Sheldrake's Experiment with Dogs -- A Telephone Experiment Indicating Human Telepathy -- Rudolph Peters and E G Recordon Observation -- Further Telepathy Experiments -- A Brief Note on Meta-Analysis -- Some Zener Card Experiments -- Ganzfeld Research -- Auto-Ganzfeld -- Auto-Ganzfeld Relating to Dream-State in the Receiver -- Spontaneous Telepathy -- Psychokinesis (PK) -- Work by Helmut Schmidt and Others -- Work on Dice Throwing -- PK Placement Study -- Explaining Psychokinesis Using Matrix Model Theory -- An Out of Body Experience -- Chapter 9 In Conclusion -- An overview -- Fields -- Telepathy: Communication Between Minds -- A Research Project to Investigate the Function of the SGU -- Missing Coding -- Evolving Paradigms -- More on the Intelligent Universe -- Humankind as the Next Effectuator -- The Mind Evolution -- References and Bibliography.
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  • 4
    Online Resource
    Online Resource
    New York, NY :Springer,
    Keywords: Insects-Physiology. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (318 pages)
    Edition: 1st ed.
    ISBN: 9781489932044
    Language: English
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  • 5
    Online Resource
    Online Resource
    Boca Raton :Taylor & Francis Group,
    Keywords: Asymmetric synthesis. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (505 pages)
    Edition: 1st ed.
    ISBN: 9781000142471
    DDC: 542.2
    Language: English
    Note: Cover -- Title Page -- Copyright Page -- The Authors -- Preface -- Table of Contents -- List of Figures -- List of Tables -- Chapter 1: Introduction -- 1.1 Nomenclature -- 1.1.1 Asymmetric Synthesis -- 1.1.2. Double Asymmetric Induction -- 1.1.3. Nomenclature Conventions -- 1.1.4. Optical Purity -- 1.2. Why Asymmetric Synthesis? -- 1.3. Methods to Achieve Asymmetric Synthesis -- 1.3.1. Transition States -- 1.3.2. Chiral Entities -- 1.3.2.1. Chiral Substrates -- 1.3.2.2. Chiral Auxiliaries -- 1.3.2.3. Self Regeneration of Stereocenters -- 1.3.2.4. Chiral Reagents -- 1.3.2.5. Chiral Environments -- 1.3.2.6. Combinations -- 1.3.2.7. The Introduction of Asymmetry -- 1.4. Resolution -- 1.4.1. Kinetic Resolution -- 1.4.2. Methods Available -- 1.5. A Question of Scale -- 1.6. Summary -- 1.7. References -- Chapter 2: General Rules -- 2.1. Carbonyl Additions -- 2.1.1. Anh-Felkin Addition -- 2.1.2. Chelation Controlled Addition -- 2.1.3. Dipolar Addition -- 2.1.4. Prelog's Rule -- 2.2. Houk' s Rule -- 2.3. Allylic Strain -- 2.4. Baldwin's Rules -- 2.4.1. Carbonyl Compounds -- 2.5. Pericyclic Transition States -- 2.5.1. Woodward-Hoffmann Rules -- 2.5.2. Stereochemical Consequences -- 2.6. Summary -- 2.7. References -- Chapter 3: One-Carbon Transformations -- 3.1. Inversions at a Single Carbon Center -- 3.1.1. Inversion of a Hydroxy Group -- 3.1.2. The Mitsunobu Reaction -- 3.2. Chiral Organometallic Reagents -- 3.3. Other Reactions -- 3.4. Summary -- 3.5. References -- Chapter 4: Reactions With Carbonyl Compounds -- 4.1. Reactions of Carbonyl Compounds With Nucleophiles -- 4.1.1. Additions of Organometallic Species to Carbonyl Compounds -- 4.1.2. Alkylating Agents -- 4.1.3. Homologation Procedures -- 4.1.4. Reactions of Vinyl Anions -- 4.1.5. Use of "Extended" Organometallic Reagents -- 4.1.5.1. Allylboranes -- 4.1.5.2. Other "Neutral" Allylic Nucleophiles. , 4.1.5.3. Allyl Anions -- 4.1.6. Reactions of Acetylene and Allenic Anions -- 4.2. Acetal Reactions -- 4.3. Other Electrophiles -- 4.4. Other Reactions -- 4.5. Reductions -- 4.5.1. Addition to Carbonyl Compounds -- 4.5.1.1. Addition to Acyclic Carbonyl Compounds -- 4.5.1.2. Addition to Cyclic Carbonyl Compounds -- 4.5.2. Addition of Hydrogen -- 4.5.3. Hydrosilylation -- 4.5.4. Metal Hydrides -- 4.5.4.1. Borohydrides -- 4.5.4.2. Lithium Aluminum Hydrides -- 4.5.5. Boron Reagents -- 4.5.6. Other Reducing Agents -- 4.6. Summary -- 4.7. References -- Chapter 5: Enolate Reactions of Carbonyl Compounds -- 5.1. Enol Ethers and Enolate Formation -- 5.2. Reactions of Enol Ethers and Enolates -- 5.2.1. Alkylation Reactions -- 5.2.2. α-Hydroxylation of Carbonyl Compounds -- 5.2.2.1. Other Methods to α-Hydroxy Carbonyl Compounds -- 5.2.3. Reactions of Enol Ethers With Other Electrophiles -- 5.3. Use of Nitrogen Derivatives -- 5.4. Asymmetric Deprotonations and Protonations -- 5.4.1. Asymmetric Deprotonations -- 5.4.2. Asymmetric Protonations -- 5.5. Summary -- 5.6. References -- Chapter 6: Reactions of Functionalized Carbonyl Systems -- 6.1. Alkylations of 1,2-Functionalized Carbonyl Compounds -- 6.1.1. Alkylations of Glycolates and Glyoxylates -- 6.1.2. Other 1,2-Functionalized Carbonyl Compounds -- 6.1.2.1. α-Hydroxy Carbonyl Compounds -- 6.1.2.2. α-Amino Carbonyl Compounds -- 6.1.2.3. Other α-Functionalized Carbonyl Compounds -- 6.2. Reductions of 1,2-Functionalized Carbonyl Compounds -- 6.2.1. 1,2-Dicarbonyl Compounds -- 6.2.2. Reductions of Other 1 ,2-Dicarbonyl Systems -- 6.2.2.1. α-Hydroxy Carbonyl Compounds -- 6.2.2.2. α-Amino Carbonyl Compounds -- 6.2.2.3. Other α-Functionalized Carbonyl Compounds -- 6.3. Alkylations of 1,3-Functionalized Carbonyl Compounds -- 6.3.1. 1,3-Dicarbonyl Alkylations -- 6.3.2. Other 1,3-Functionalized Carbonyl Compounds. , 6.3.2.1. β-Hydroxy and Amino Carbonyl Compounds -- 6.3.2.2. Other β-Functionalized Carbonyl Compounds -- 6.4. Reductions of 1,3-Functionalized Carbonyl Compounds -- 6.4.1. 1,3-Dicarbonyl Reductions -- 6.4.2. Reductions of Other 1,3-Functionalized Carbonyl Compounds -- 6.4.2.1. Reductions of 13-Hydroxy and Amino Carbonyl Compounds -- 6.4.2.2. Other 13-Functionalized Carbonyl Compounds -- 6.5. Other Systems -- 6.5.1. Reactions of Anhydrides and Related Systems -- 6.6. Summary -- 6.7. References -- Chapter 7: Aldol and Related Reactions -- 7.1. The Aldol Reaction: Methods of Control -- 7.2. The Aldol Reaction: The Role of Enolate Geometry and Metal Counterion -- 7.2.1. Boron Enolates -- 7.2.2. Lithium Enolates -- 7.2.3. Magnesium Enolates -- 7.2.4. Silyl Enol Ethers -- 7.2.5. Tin Compounds -- 7.2.6. Titanium Enolates -- 7.2.7. Zinc Enolates and the Reformatsky Reaction -- 7.3. The Formose Reaction -- 7.4. Summary -- 7.5. References -- Chapter 8: Preparation and Reactions of Alkenes -- 8.1. Alkene Synthesis -- 8.1.1. Alkyne Reductions and Additions -- 8.1.1.1. Simple Alkenes -- 8.1.1.2. Conjugated Alkenes -- 8.1.1.3. Heteroatom Substituted Alkenes -- 8.1.1.4. Allyl Alcohols and Related Compounds -- 8.1.2. Reaction of Organometallics With Carbonyl Compounds -- 8.1.2.1. Simple Alkenes -- 8.1.2.1.1. The Wittig Reaction -- 8.1.2.1.2. The Peterson Reaction -- 8.1.2.1.3. The Julia Reaction -- 8.1.2.1.4. Trisubstituted Alkenes -- 8.1.2.1.5. Additional Variants to the Wittig Reaction -- 8.1.2.1.5.1. The Boron-Wittig Reaction -- 8.1.2.1.6. Alternate Routes -- 8.1.2.2. Conjugated Alkenes -- 8.1.2.3. Heteroatom Substituted Alkenes -- 8.1.2.4. Allylic Compounds -- 8.1.3. Reaction of Heteroalkenes -- 8.1.3.1. Simple Alkenes -- 8.1.3.2. Conjugated Alkenes -- 8.1.3.3. Heteroatom Substitution -- 8.1.3.4. Allylic Compounds -- 8.1.4. Eliminations -- 8.1.5. Inversion. , 8.2. Reactions of Alkenes -- 8.2.1. Addition Reactions -- 8.2.1.1. Addition of Acids -- 8.2.1.2. Addition of Halogens -- 8.2.1.3. Oxymercuration -- 8.2.2. Reductions -- 8.2.2.1. Hydrogenations -- 8.2.2.2. Hydrosilylations -- 8.2.2.3. Hydroboration -- 8.2.3. Allylic Functionalization -- 8.3. Summary -- 8.4. References -- Chapter 9: Reactions of Functionalized Alkenes -- 9.1. Hydrogenations -- 9.1.1. Functionalized Alkenes -- 9.1.2. Allylic Substrates -- 9.2. Other Transition Metal Catalyzed Reactions -- 9.2.1. Isomerizations -- 9.2.2. Hydrosilylations -- 9.2.3. Hydroformylations -- 9.2.4. Hydrocarboxylations and Hydroesterifications -- 9.3. Hydride Delivery Agents -- 9.3.1. Hydroborations of Allyl Systems -- 9.4. Reactions of Some Functionalized Alkenes -- 9.4.1. Reactions of Functionalized Silanes -- 9.4.2. Propargylic Substrates -- 9.4.3. Vinyl Compounds -- 9.5. Conjugate Additions -- 9.5.1. α,β-Unsaturated Carbonyl Systems -- 9.5.1.1. Carbon Nucleophiles -- 9.5.1.2. Conjugate Reductions -- 9.5.1.3. Other Nucleophiles -- 9.5.2. Other Systems -- 9.6. Allyl Alkylations -- 9.7. Other Reactions -- 9.8. Summary -- 9.9. References -- Chapter 10: Asymmetric Oxidations of Isolated Alkenes -- 10.1. Epoxidations -- 10.1.1. Peroxy Acid Epoxidation -- 10.1.2. Oxaziridine Epoxidation -- 10.1.3. Metal Catalyzed Epoxidations -- 10.1.4. Other Epoxidation Methods -- 10.2. Reactions of Epoxides -- 10.3. 1,2-Diols -- 10.3.1. Metal Oxide Additions -- 10.3.2. Osmium Reagents -- 10.4. Formation and Reactions of Cyclic Sulfates -- 10.5. Preparation and Reactions of Aziridines -- 10.6. Summary -- 10.7. References -- Chapter 11: Oxidations of Functionalized Alkenes -- 11.1. Epoxidation of Allyl Alcohols -- 11.1.1. Metal Catalyzed Oxidations -- 11.1.1.1. With Vanadium -- 11.1.1.2. Molybdenum -- 11.1.1.3. Tungsten -- 11.1.1.4. Other Metals -- 11.1.2. Sharpless Epoxidation. , 11.1.2.1. Kinetic Resolution With The Sharpless Epoxidation Procedure -- 11.1.3. Peroxy Acid Oxidations of AllyI Alcohols -- 11.1.4. Other Methods to 2,3-Epoxy Alcohols -- 11.2. Reactions of 2,3-Epoxy Alcohols and Related Systems -- 11.2.1. Oxygen Nucleophiles -- 11.2.2. Nitrogen-Containing Nucleophiles -- 11.2.3. Sulfur Nucleophiles -- 11.2.4. Reactions Involving Cyclic Intermediates -- 11.2.5. Organometallic Reagents -- 11.2.6. Oxidations -- 11.2.7. Other Reactions -- 11.2.8. Reactions of Modified 2,3-Epoxy Alcohols -- 11.3. Epoxidations and Reactions of Other Unsaturated Systems -- 11.3.1. Conjugated Enones -- 11.3.1.1. Epoxidation -- 11.3.1.2. Reactions -- 11.3.2. α,β-Unsaturated Esters -- 11.3.2.1. Epoxidation -- 11.3.2.2. Dihydroxylation -- 11.3.2.3. Reactions -- 11.3.3. α,β-Unsaturated Acids -- 11.3.3.1. Epoxidation -- 11.3.3.2. Reactions -- 11.3.4. Epoxides from Homoallyl Alcohols -- 11.3.5. Conjugated Dienes -- 11.3.5.1 Epoxidation -- 11.3.5.2. Reactions -- 11.3.6. Other Systems -- 11.4. Other Oxidations -- 11.4.1. Osmylation -- 11.5. Other Systems -- 11.6. Summary -- 11.7. References -- Chapter 12: Pericyclic Reactions -- 12.1. The Diels-Alder Reaction -- 12.1.1. Regio- and Stereochemistry -- 12.1.2. Chiral Dienophiles -- 12.1.3. Lewis Acids -- 12.1.3.1. Chiral Lewis Acids -- 12.1.4. Chiral Dienes -- 12.1.5. Cooperative Blocking Groups -- 12.1.6. Biological Catalysts -- 12.1.7. Chiral Bases -- 12.1.8. Solvents Effects -- 12.1.9. Pressure Effects -- 12.1.10. Intramolecular Diels-Alder Reactions -- 12.1.11. Retro Diels-Alder Reactions -- 12.1.12. Inverse Electron Demand Diels-Alder Reactions -- 12.1.13. Reactions of Dienes with Carbonyl Compounds -- 12.1.13.1. Related Cycloaddition Reactions -- 12.2. Claisen Rearrangements -- 12.2.1. Cope Rearrangement -- 12.2.2. Claisen Rearrangement -- 12.2.3. Ester Enolate Claisen Rearrangement. , 12.3. Ene Reaction.
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  • 6
    Online Resource
    Online Resource
    New York, NY :Springer,
    Keywords: Electrons-Diffraction. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (198 pages)
    Edition: 1st ed.
    ISBN: 9781489964755
    DDC: 548/.83
    Language: English
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  • 7
    Type of Medium: Book
    Pages: Graph. Darst., Kt. , XIII, 308 S.
    Language: English
    Note: New Haven, Conn., Yale Univ., Diss., 1979
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  • 8
    Keywords: Aquatic resources conservation Congresses ; Aquatic resources Congresses ; Aquatic ecology Congresses ; Konferenzschrift ; Konferenzschrift 1970 ; Ökosystem ; Wasser ; Wasser
    Type of Medium: Book
    Pages: XV, 318 S , Ill
    ISBN: 0126133298
    Series Statement: Symposia of the Zoological Society of London 29
    DDC: 591/.08 s
    Language: English
    Note: Includes bibliographies
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  • 9
    Online Resource
    Online Resource
    New York : Oxford University Press
    Keywords: Philosophy of mind. ; Consciousness. ; Mind and body. ; Dualism. ; Philosophy of mind ; Consciousness ; Mind and body ; Dualism ; Dualism ; Mind and body ; Consciousness ; Philosophy of mind ; Philosophy of mind. ; Consciousness. ; Mind and body. ; Dualism. ; Consciousness ; Philosophy ; PHILOSOPHY ; Mind & Body ; Consciousness ; Dualism ; Mind and body ; Bewustzijn ; Theorievorming ; Philosophy of Mind ; Reduktionismus ; Leib-Seele-Problem ; Philosophie ; Kognitionswissenschaft ; Esprit et corps ; Théorie de la connaissance ; Conscience ; Philosophie de l'esprit ; Dualisme ; Esprit ; Medvetandefilosofi ; Medvetandet ; Kropp och själ ; Philosophy of mind ; Bewusstsein ; Electronic books. ; Electronic books. ; Electronic books ; Philosophy of Mind ; Bewusstsein
    Description / Table of Contents: 1. Two Concepts of Mind -- 2. Supervenience and Explanation -- 3. Can Consciousness Be Reductively Explained? -- 4. Naturalistic Dualism -- 5. The Paradox of Phenomenal Judgment -- 6. The Coherence Between Consciousness and Cognition -- 7. Absent Qualia, Fading Qualia, Dancing Qualia -- 8. Consciousness and Information: Some Speculation -- 9. Strong Artificial Intelligence -- 10. The Interpretation of Quantum Mechanics.
    Type of Medium: Online Resource
    Pages: xvii, 414 p , 25 cm
    Edition: Boulder, Colo NetLibrary 2001 Online-Ressource E-Books von NetLibrary
    ISBN: 0585353131 , 9780585353135
    Series Statement: Philosophy of mind series
    Language: English
    Note: Includes bibliographical references (p. [391]-404) and index , Electronic reproduction, Boulder, Colo : NetLibrary, 2001
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  • 10
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Studies on the Reactivity of Metal π-Complexes, XXII. Sandwich-like Dinuclear (Pd-Pd)-Complexes with Bridging Cyclopentadienyl and Allyl LigandsThe reaction of C5H5Pd(2-RC3H4) (2-RC3H4 = 2-R-allyl) with tertiary phosphines or phosphites in the molar ratio of 1:1 produces in practically quantitative yields the dinuclear complexes (C5H5)(2-RC3H4)Pd2L2 (4-20) in which palladium has the oxidation state +1. The crystal structure analysis of 5 (R = CH3, L = P(C6H5)3) and 12 (R = CH3, L = P(OC6H4-o-CH3)3) shows that the cyclopentadienyl as well as the allyl ligand is bonded in a sandwich manner to the Pd-Pd unit. The Pd-Pd distance of 267.9 (in 5) or 268.9 pm (in 12) is suggestive of a metal-metal bond. It is not possible to determine whether the cyclopentadienyl ring in 4-20 exists as a pentahapto- or trihapto-bonded ligand on the basis of the 1H- and 13C n. m. r. data. The reactivity of the dinuclear complexes is in agreement with square planar coordination of the metal atoms.
    Notes: Bei den Reaktionen von C5H5Pd(2-RC3H4) (2-RC3H4 = 2-R-Allyl) mit tertiären Phosphinen oder Phosphiten im Molverhältnis 1:1 entstehen in praktisch quantitativer Ausbeute die Zweikernkomplexe (C5H5)(2-RC3H4)Pd2L2 (4-20), in denen Palladium in der Oxidationszahl +1 vorliegt. Wie die Kristallstrukturanalysen von 5 (R = CH3, L = P(C6H5)3) und 12 (R = CH3, L = P(OC6H4-o-CH3)3) zeigen, sind sowohl der Cyclopentadienyl- als auch der Allyl-Ligand sandwichartig an die Pd2-Einheit gebunden. Der Pd-Pd-Abstand von 267.9 (in 5) bzw. 268.9 pm (in 12) weist auf das Vorliegen einer Metall-Metall-Bindung hin. Aufgrund der 1H- und 13C-NMR-Daten ist nicht zu entscheiden, ob in 4-20 der Cyclopentadienylring als pentahapto-oder trihapto-gebundener Ligand vorliegt. Die Reaktivität der Zweikernkomplexe steht mit einer quadratisch-planaren Koordination der Metallatome in Einklang.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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