|
|
|
|
LEADER |
00000cam a2200000 i 4500 |
001 |
SCIDIR_on1028979400 |
003 |
OCoLC |
005 |
20231120010248.0 |
006 |
m o d |
007 |
cr cnu|||unuuu |
008 |
180319s2018 enk ob 001 0 eng d |
040 |
|
|
|a N$T
|b eng
|e rda
|e pn
|c N$T
|d N$T
|d YDX
|d OPELS
|d NLE
|d OCLCF
|d STF
|d SNK
|d MERER
|d D6H
|d OCLCQ
|d INT
|d OCLCQ
|d UKMGB
|d U3W
|d LVT
|d OCLCQ
|d LQU
|d S2H
|d OCLCO
|d OCLCQ
|d OCLCO
|d K6U
|d OCLCQ
|d SFB
|d OCLCQ
|d OCLCO
|
016 |
7 |
|
|a 018809347
|2 Uk
|
019 |
|
|
|a 1029229119
|a 1029325113
|a 1029447142
|a 1105193317
|a 1105562857
|a 1151762846
|
020 |
|
|
|a 9780128122853
|q (electronic bk.)
|
020 |
|
|
|a 0128122854
|q (electronic bk.)
|
020 |
|
|
|z 9780128122846
|
020 |
|
|
|z 0128122846
|
035 |
|
|
|a (OCoLC)1028979400
|z (OCoLC)1029229119
|z (OCoLC)1029325113
|z (OCoLC)1029447142
|z (OCoLC)1105193317
|z (OCoLC)1105562857
|z (OCoLC)1151762846
|
050 |
|
4 |
|a QD281.A6
|
072 |
|
7 |
|a SCI
|x 013040
|2 bisacsh
|
082 |
0 |
4 |
|a 547/.27
|2 23
|
100 |
1 |
|
|a Shi, Feng,
|e author.
|
245 |
1 |
0 |
|a Catalytic amination for N-alkyl amine synthesis /
|c Feng Shi, Xinjiang Cui.
|
264 |
|
1 |
|a London :
|b Academic Press,
|c [2018]
|
300 |
|
|
|a 1 online resource
|
336 |
|
|
|a text
|b txt
|2 rdacontent
|
337 |
|
|
|a computer
|b c
|2 rdamedia
|
338 |
|
|
|a online resource
|b cr
|2 rdacarrier
|
504 |
|
|
|a Includes bibliographical references and index.
|
588 |
|
|
|a Online resource; title from PDF title page (EBSCO, viewed March 22, 2018).
|
520 |
|
|
|a Catalytic Amination for N-Alkyl Amine Synthesis provides a useful survey of this key type of reaction for chemistry researchers in academia and industry. Beginning with an introduction to amination and the development of the field, the book focuses on useful and high potential methods, such as the catalytic amination of alcohol with homogeneous and heterogeneous catalysts, the coupling reaction of olefin and amine, and the reductive amination of carbon dioxide with different reducing agents. The work also discusses two key examples of one-pot synthesis, the oxidative amination of alkane and amine and synthesis of N-alkyl amine with nitrobenzene and nitrile as starting materials. Valuable for chemists, materials scientists, chemical engineers and others, the book offers a unique overview of this growing area and its future possibilities.
|
505 |
0 |
|
|a 1. Introduction and background; 2. Catalytic amination of alcohol; 3. Catalytic amination of olefin; 4. Catalytic amination of carbon dioxide; 5. Oxidative amination of alkane; 6. Reductive amination with nitrobenzene and nitrile as starting materials; 7. Amination reactions with ammonia.
|
650 |
|
0 |
|a Amination.
|
650 |
|
0 |
|a Nitrogen compounds.
|
650 |
|
2 |
|a Amination
|0 (DNLM)D000586
|
650 |
|
2 |
|a Nitrogen Compounds
|0 (DNLM)D017672
|
650 |
|
6 |
|a Amination.
|0 (CaQQLa)201-0267949
|
650 |
|
6 |
|a Azote
|x Compos�es.
|0 (CaQQLa)201-0001053
|
650 |
|
7 |
|a nitrogen compounds.
|2 aat
|0 (CStmoGRI)aat300210801
|
650 |
|
7 |
|a SCIENCE
|x Chemistry
|x Organic.
|2 bisacsh
|
650 |
|
7 |
|a Amination
|2 fast
|0 (OCoLC)fst00807594
|
650 |
|
7 |
|a Nitrogen compounds
|2 fast
|0 (OCoLC)fst01038065
|
700 |
1 |
|
|a Cui, Xinjiang,
|e author.
|
776 |
0 |
8 |
|i Print version:
|z 0128122846
|z 9780128122846
|w (OCoLC)1011515714
|
856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/book/9780128122846
|z Texto completo
|