Carbon–carbon bond formation promoted by electrophiles and the mechanism of the Fischer–Tropsch reaction

1983 ◽  
pp. 166-167 ◽  
Author(s):  
Andrew Nutton ◽  
Amelio Vázquez de Miguel ◽  
Kiyoshi Isobe ◽  
Peter M. Maitlis
Keyword(s):  
Bond Formation ◽  
Fischer Tropsch ◽  
Carbon Bond ◽  
Carbon Carbon Bond

Carbon-Carbon bond formation during Fe catalyzed Fischer-Tropsch synthesis

2020 ◽  
Vol 602 ◽  
pp. 117607
Author(s):  
Buchang Shi ◽  
Yunxin Liao ◽  
Zachary J. Callihan ◽  
Brad T. Shoopman ◽  
Mingsheng Luo
Keyword(s):  
Bond Formation ◽  
Tropsch Synthesis ◽  
Fischer Tropsch ◽  
Carbon Bond ◽  
Fischer Tropsch Synthesis ◽  
Carbon Carbon Bond

Carbon-carbon bond formation at dinuclear metal centres

1982 ◽  
Vol 308 (1501) ◽  
pp. 67-73 ◽  
Keyword(s):  
Metal Surface ◽  
Related Species ◽  
Bond Formation ◽  
Surface Processes ◽  
Formation Processes ◽  
Fischer Tropsch ◽  
Unsaturated Hydrocarbons ◽  
Carbon Bond ◽  
Fischer Tropsch Synthesis ◽  
Carbon Carbon Bond

The Fischer-Tropsch synthesis of hydrocarbons probably involves an array of carbon-carbon bond-formation processes occurring to unite carbene, carbyne, alkyl, olefin, and related species on a metal surface. In seeking to understand the nature of such processes, model diruthenium complexes have been prepared and the products of their thermolysis and reactions with unsaturated hydrocarbons investigated. The combination at a diruthenium centre of two carbenes, of a carbene and an alkyne, and of a carbyne and an olefin is described, and the possible implications for metal surface processes are emphasized.

scholarly journals Mechanistic insight into carbon-carbon bond formation on cobalt under simulated Fischer-Tropsch synthesis conditions

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
C. J. (Kees-Jan) Weststrate ◽  
Devyani Sharma ◽  
Daniel Garcia Rodriguez ◽  
Michael A. Gleeson ◽  
Hans O. A. Fredriksson ◽  
...  
Keyword(s):  
Bond Formation ◽  
Tropsch Synthesis ◽  
Fischer Tropsch ◽  
Carbon Bond ◽  
Fischer Tropsch Synthesis ◽  
Synthesis Conditions ◽  
Mechanistic Insight ◽  
Carbon Carbon Bond ◽  
Insight Into

Carbon Dioxide-Mediated C(sp2)–H Arylation of Primary and Secondary Benzylamines

2018 ◽  
Author(s):  
Mohit Kapoor ◽  
Pratibha Chand-Thakuri ◽  
Michael Young
Keyword(s):  
Carbon Dioxide ◽  
Transition Metal ◽  
Bond Activation ◽  
Bond Formation ◽  
Carbon Bond ◽  
Chelate Effect ◽  
Free Amine ◽  
Carbon Carbon Bond ◽  
New Strategy ◽  
Metal Catalyzed

Carbon-carbon bond formation by transition metal-catalyzed C–H activation has become an important strategy to fabricate new bonds in a rapid fashion. Despite the pharmacological importance of <i>ortho</i>-arylbenzylamines, however, effective <i>ortho</i>-C–C bond formation from C–H bond activation of free primary and secondary benzylamines using Pd<sup>II</sup> remains an outstanding challenge. Presented herein is a new strategy for constructing <i>ortho</i>-arylated primary and secondary benzylamines mediated by carbon dioxide (CO<sub>2</sub>). The use of CO<sub>2</sub> is critical to allowing this transformation to proceed under milder conditions than previously reported, and that are necessary to furnish free amine products that can be directly used or elaborated without the need for deprotection. In cases where diarylation is possible, a chelate effect is demonstrated to facilitate selective monoarylation.

Modern Organic Synthesis in the Laboratory

2008 ◽  
Author(s):  
Jie Jack Li ◽  
Chris Limberakis ◽  
Derek A. Pflum
Keyword(s):  
Organic Chemistry ◽  
Graduate Students ◽  
Organic Synthesis ◽  
Functional Group ◽  
Bond Formation ◽  
Reaction Conditions ◽  
Carbon Bond ◽  
Oxidation Reduction ◽  
Carbon Carbon Bond ◽  
Daunting Task

Searching for reaction in organic synthesis has been made much easier in the current age of computer databases. However, the dilemma now is which procedure one selects among the ocean of choices. Especially for novices in the laboratory, it becomes a daunting task to decide what reaction conditions to experiment with first in order to have the best chance of success. This collection intends to serve as an "older and wiser lab-mate" one could have by compiling many of the most commonly used experimental procedures in organic synthesis. With chapters that cover such topics as functional group manipulations, oxidation, reduction, and carbon-carbon bond formation, Modern Organic Synthesis in the Laboratory will be useful for both graduate students and professors in organic chemistry and medicinal chemists in the pharmaceutical and agrochemical industries.

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