Modern synthesis processes and reactivity of fluorinated compounds /

Bibliographic Details
Corporate Author:	ScienceDirect (Online service)
Other Authors:	Groult, Henri (Editor), Leroux, Frédéric (Editor), Tressaud, Alain (Editor)
Format:	eBook
Language:	English
Published:	Amsterdam ; Boston : Academic Press, an imprint of Elsevier, [2017]
Series:	Progress in fluorine science series.
Subjects:	Fluorine compounds > Synthesis. Fluorine compounds > Reactivity. Electronic books.
Online Access:	Connect to the full text of this electronic book

Table of Contents:

Front Cover; Modern Synthesis Processes and Reactivity of Fluorinated Compounds; Progress in Fluorine Science Series; Modern Synthesis Processes and Reactivity of Fluorinated Compounds: Progress in Fluorine Science Series; Copyright; Contents; List of Contributors; Foreword; 1
The Cosmic Origin of Fluorine: An Astronomer's View on Fluorine Synthesis; 1. The Cosmic Origin of the Elements; 2. The Cosmic Origin of Fluorine; 2.1 Theoretical Ideas; 2.2 Observations; 2.3 What the Future Holds; References.
2
The Fluorine Atom in Health Care and Agrochemical Applications: A Contribution to Life Science1. Introduction; 1.1 The History of Fluorine in Pharmaceutical Applications; 1.2 The History of Fluorine in Agrochemical Applications; 2. Methods to Introduce Fluorine Into Organic Molecules; 2.1 Fluorinating Agents; 2.2 Use of Anhydrous HF; 2.3 Indirect Fluorination: Use of a Building Block Containing a Fluorinated Group; 3. Use of Trifluoromethyl Group in Pharmaceuticals and Agrochemistry; 3.1 Synthesis of Trifluoroacetyl Chloride and Trifluoroacetic Acid.
3.2 Some Active Agrochemical Ingredients Based on Aliphatic Trifluoromethylated Building Blocks3.3 Some Active Pharmaceutical Ingredients Based on Aliphatic Trifluoromethylated Building Blocks; 4. Use of Difluoromethyl Group in Pharmaceuticals and Agrochemistry; 4.1 Synthesis Strategy to Obtain CF2 Groups in Active Ingredients; 4.2 Examples of Active Ingredients Containing the CF2 Group; 4.3 Use of Difluoromethanesulfonyl Chloride; References; 3
Industrial Syntheses of Hydrohaloolefins and Related Products; 1. Introduction; 2. Hydrofluoroolefins.
2.1 CHFCF2, 1,1,2-Trifluoroethylene or HFO-11232.2 E, Z-CF3CHHF, 1,3,3,3-Tetrafluoropropene or HFO-1234ze; 2.3 CF3CFCH2, 2,3,3,3-Tetrafluoro-1-propene or HFO-1234yf; 2.3.1 Hexafluoropropene Route; 2.3.2 Tetrafluoroethylene (CF2CF2) Routes; 2.3.3 Tetrafluoroethylene-Chloroform Route; 2.3.4 1230xa (CCl2CClCH2Cl) Route; 2.3.5 240db (CCl3CClHCH2Cl) Route; 2.3.6 1243zf (CF3CHCH2) Route; 2.3.7 114a (CF2ClCF2Cl) and Formaldehyde Route; 2.3.8 Thermal Pyrolysis Processes; 2.4 CF3CFCHF, 1,2,3,3,3-Pentafluoro-1-propene or HFO-1225ye; 2.4.1 Hexafluoropropene Route; 2.4.2 Tetrafluoroethylene Routes.
2.4.3 Tetrafluoroethylene-CFC-12 (CCl2F2) Route2.5 CF3CHCH2, 3,3,3-Trifluoropropene or HFO-1243zf; 2.6 Z-CF3CHCHCF3, 1,1,1,4,4,4-Hexafluoro-2-butene, Z-1336mzz; 2.7 E-CF3CHCHCF3, (E)-1,1,1,4,4,4-Hexafluorobut-2-ene, E-1336mzz; 3. Other Hydrofluoroolefins; 4. Hydrochlorofluoroolefins; 4.1 E-CF3CHCHCl, E-3,3,3-Trifluoro-1-chloropropene, E-1233zd; 4.2 Z-CF3CHCHCl, E-3,3,3-Trifluoro-1-chloropropene, E-1233zd; 4.3 CF3CClCH2, 3,3,3-Trifluoro-2-chloro-1-propene, HFCO-1233xf; 4.3.1 1230xa (CCl2CClCH2Cl) Route; 4.3.2 2,3,3,3-Tetrachloropropene (CCl3CClCH2) 1230xf Route.