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Titlebook: Alkane C-H Activation by Single-Site Metal Catalysis; Pedro J. Pérez Book 2012 Springer Science+Business Media Dordrecht 2012 Alkane trans

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31#
發(fā)表于 2025-3-26 22:00:17 | 只看該作者
,Catalytic Carbon–Boron Bond Formation via Activation of Alkane C–H Bonds,s, although they are abundant natural resources, alkanes are notoriously underutilized in chemical synthesis, and the selective functionalization of alkane to produce useful organic products is a major challenge in organic chemistry. Among different C–H functionalization methods of alkanes, transiti
32#
發(fā)表于 2025-3-27 02:04:48 | 只看該作者
Alkane Dehydrogenation,y. The dehydrogenation of alkanes, the most abundant and inexpensive hydrocarbons, is a simple and attractive route for producing alkenes. This chapter addresses the challenges presented by the activation of strong C–H bonds present in alkanes and the ongoing need for the development of efficient an
33#
發(fā)表于 2025-3-27 07:43:08 | 只看該作者
,Alkane C–H Oxygenation Catalyzed by Transition Metal Complexes,enges to the design of reagents that could enable their selective oxidation. Highly reactive-oxidizing reagents are needed, and this factor poses major problems in terms of chemo and regioselectivity. Despite all these conditionings, because of its technological and biological significance and impli
34#
發(fā)表于 2025-3-27 11:37:04 | 只看該作者
Alkane Catalytic Functionalization by Carbene or Nitrene Insertion Reactions,er. Developed at different extends, the former methodology has received much attention, probably due to the use of available diazo compounds as the carbene source. For the NR case, the sources are usually based in hypervalent iodine compounds. In both cases, a yet reduced number of catalytic systems
35#
發(fā)表于 2025-3-27 16:08:18 | 只看該作者
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36#
發(fā)表于 2025-3-27 19:36:40 | 只看該作者
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