If you wish to place a tax exempt order please contact us. Chapter Two. Add to cart. Sales tax will be calculated at check-out. Free Global Shipping. Description Modern Synthesis Processes and Reactivity of Fluorinated Compounds focuses on the exceptional character of fluorine and fluorinated compounds. This comprehensive work explores examples taken from all classes of fluorine chemistry and illustrates the extreme reactivity of fluorinating media and the peculiar synthesis routes to fluorinated materials.
The book provides advanced and updated information on the latest synthesis routes to fluorocompounds and the involved reaction mechanisms.
Special attention is given to the unique reactivity of fluorine and fluorinated media, along with the correlation of those properties to valuable applications of fluorinated compounds. Contains quality content edited, and contributed, by leading scholars in the field Presents applied guidance on the preparation of original fluorinated compounds, potentially transferable from the lab scale to industrial applications Provides practical synthesis information for a wide audience interested in fluorine compounds in many branches of chemistry, materials science, and physics.
Chapter One. The Cosmic Origin of the Elements 2. Introduction 2. Use of Trifluoromethyl Group in Pharmaceuticals and Agrochemistry 4. Use of Difluoromethyl Group in Pharmaceuticals and Agrochemistry 3. Industrial Syntheses of Hydrohaloolefins and Related Products 1. Hydrofluoroolefins 3. Other Hydrofluoroolefins 4. Hydrochlorofluoroolefins 5. Conclusion 4. Introduction and Historical Overview 2. Mechanism of Electrochemical Fluorination Simons Process 4. Electrochemical Fluorination of the Elementorganic Compounds 5.
Conclusions 6. Indirect Methods 3. Direct Preparation: Trifluoromethylthiolation 4. Conclusions 7. Trifluoromethylation Reactions 3. Difluoromethylation Reactions 4.
Conclusion 8. Oxidative Trifluoromethylation and Trifluoromethylthiolation 1. Oxidative Trifluoromethylation 3. Oxidative Trifluoromethylthiolation 4. Other Oxidative Fluoroalkylations 5. Conclusion 9. Catalytic Enantioselective Fluorination 1. Electrophilic Fluorination Methods 3. Elder, Alvin A. Arens, Mark S. David Irwin, R. Garrett, M. Goldstein, David C. Lay, David I. Schneider, Nakhle H. Asmar Solutions Manual Calculus 9th Ed. Hostetler, Bruce H. Adams and C.
Goldstein, David I. Schneider, David I. Lay, Nakhle H. Henry Edwards, David E. Marsden, A. Lial , Raymond N. Greenwell, Nathan P. Heald, Jerry B. Leonard, J. Lewis, A. Liu, G. Allen, Douglas R. Ross, Randolph W. Horngren, Srikant M. Datar, Madhav V. McCormac and Russell H. Devore, Matthew A. Lee, David G. Diniz, Eduardo A. Kulakowski , F. Kothari, I. Bard and Larry R. Faulkner and Cynthia G. Woodson, James R. Boyce and Richard C.
Kohler, Lee W. Cover, Joy A. Hayt Jr. Crowe, Donald F. Elger, John A. Roberson and Barbara C. Meriam, L. Solutions Manual Engineering Statistics 4th Ed. Brigham, Michael C. Copeland J. Reitz, Frederick J. Pritchard, John W. Skoog, Donald M. West, F. James Holler, Stanley R. Jordan , Stephen A. Schilling, Sandra L. Alexander M. Moran, Howard N. Shapiro, Daisie D. Boettner, Margaret B. Munson, Donald F. Young, Theodore H.
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Asymptotic Minimax Theory by Korostelev A. Simon , Lawrence E. Knight, Malvin A.
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