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m o d |
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161110s2017 ne o 000 0 eng d |
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20260609153419.4 |
| 020 |
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|a 9780128037904
|q electronic book
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|a 0128037903
|q electronic book
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|z 9780128037409
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|z 0128037407
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| 024 |
8 |
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|a 99970592212
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|a (NhCcYBP)ybp13251371
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|a NhCcYBP
|c NhCcYBP
|d UtOrBLW
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4 |
|a QD181.F1
|b M63 2017
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| 072 |
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7 |
|a SCI
|x 013030
|2 bisacsh
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| 082 |
0 |
4 |
|a 546.731
|2 23
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| 245 |
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|a Modern synthesis processes and reactivity of fluorinated compounds /
|c edited by Henri Groult, Frédéroc R. Leroux, Alain Tressaud.
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| 264 |
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1 |
|a Amsterdam ;
|a Boston :
|b Academic Press, an imprint of Elsevier,
|c [2017]
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| 300 |
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|a 1 online resource.
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| 336 |
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|a text
|b txt
|2 rdacontent
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| 337 |
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|a computer
|b c
|2 rdamedia
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| 338 |
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|a online resource
|b cr
|2 rdacarrier
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| 490 |
1 |
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|a Progress in fluorine science series ;
|v Vol. 3
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| 505 |
0 |
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|a 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.
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| 505 |
8 |
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|a 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.
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| 505 |
8 |
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|a 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.
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| 505 |
8 |
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|a 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.
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| 505 |
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|a 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.
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| 588 |
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|a Description based on online resource; title from digital title page (viewed on February 14, 2017).
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| 500 |
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|a Electronic resource.
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| 650 |
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0 |
|a Fluorine compounds
|x Synthesis.
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| 650 |
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0 |
|a Fluorine compounds
|x Reactivity.
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| 655 |
|
7 |
|a Electronic books.
|2 local
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| 700 |
1 |
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|a Groult, Henri,
|e editor.
|0 http://id.loc.gov/authorities/names/n2004016394
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| 700 |
1 |
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|a Leroux, Frédéric,
|e editor.
|
| 700 |
1 |
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|a Tressaud, Alain,
|e editor.
|0 http://id.loc.gov/authorities/names/n99038962
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| 710 |
2 |
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|a ScienceDirect (Online service)
|0 http://id.loc.gov/authorities/names/no00037061
|
| 776 |
1 |
8 |
|i Print version:
|t Modern Synthesis Processes and Reactivity of Fluorinated Compounds.
|d Elsevier Science Ltd 2016
|z 9780128037409
|z 0128037407
|
| 830 |
|
0 |
|a Progress in fluorine science series.
|0 http://id.loc.gov/authorities/names/no2016067092
|
| 856 |
4 |
0 |
|u http://proxy.library.tamu.edu/login?url=https://www.sciencedirect.com/science/book/9780128037409
|z Connect to the full text of this electronic book
|t 0
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| 955 |
|
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|a YBP purchased firm e-records
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| 980 |
|
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|b 338.00
|g 1
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| 999 |
f |
f |
|s 5ff37b3b-f95f-3188-bf28-196bc9a28174
|i 45d387b8-afe9-38a0-81c7-82e769918d5d
|t 0
|
| 952 |
f |
f |
|a Texas A&M University
|b College Station
|c Electronic Resources
|s www_evans
|d Available Online
|t 0
|e QD181.F1 M63 2017
|h Library of Congress classification
|
| 998 |
f |
f |
|a QD181.F1 M63 2017
|t 0
|l Available Online
|