scholarly journals Transition metal-catalyzed alkene isomerization as an enabling technology in tandem, sequential and domino processes

2021 ◽  
Author(s):  
Daniele Fiorito ◽  
Simone Scaringi ◽  
Clément Mazet

One-pot reactions based on catalytic isomerization of alkenes not only offer the inherent advantages of atom-, step- and redox-economy but also enable the preparation of value-added products that would be difficult to access by conventional methods.

2016 ◽  
Vol 14 (6) ◽  
pp. 1853-1914 ◽  
Author(s):  
Markus D. Kärkäs ◽  
Bryan S. Matsuura ◽  
Timothy M. Monos ◽  
Gabriel Magallanes ◽  
Corey R. J. Stephenson

Recent advances in transition-metal catalyzed depolymerization of lignin to value-added products are discussed in this review.


2020 ◽  
Vol 508 ◽  
pp. 119654
Author(s):  
Antônio E.M. Crotti ◽  
Daniel Previdi ◽  
Paulo M. Donate ◽  
J. Scott McIndoe

2019 ◽  
Vol 4 (1) ◽  
pp. 100-104 ◽  
Author(s):  
Saeed Bahadorikhalili ◽  
Golnaz Rahimzadeh ◽  
Ebrahim Kianmehr ◽  
Samira Ansari ◽  
Haleh Hamedifar ◽  
...  

2020 ◽  
Vol 74 (11) ◽  
pp. 871-877
Author(s):  
Sara Mazeh ◽  
Maria Ivana Lapuh ◽  
Tatiana Besset

Thanks to the unique features of the fluorine atom and the fluorinated groups, fluorine-containing molecules are essential. Therefore, the search for new fluorinated groups as well as straightforward and original methodologies for their installation is of prime importance. Especially, the combination of organofluorine chemistry with transition metal-catalyzed C–H bond functionalization reactions offered straightforward tools to access original fluorinated scaffolds. In this context, over the last years, our group focused on the development of original methodologies to synthesize fluorine-containing molecules with a special attention to emergent fluorinated groups. The present account highlights our recent contributions to the synthesis of highly value-added fluorine-containing compounds by transition metal-catalyzed C–H bond activation.


2020 ◽  
Author(s):  
Antonio Crotti ◽  
Daniel Previdi ◽  
Paulo Donate ◽  
J Scott McIndoe

In this paper, pressurized sample infusion electrospray ionization mass spectrometry (PSI-ESI-MS) and FTIR spectroscopy was used to investigate the mechanism of a like-Barbier cobalt-mediated one-pot transition metal-catalyzed multicomponent reaction (MCR). The use of charge-tagged aryl halides allowed for the detection of cobalt(II)-promoted hydrodehalogenation products. Although these products were also detected in the off-line ESI-MS monitoring, the ability of PSI-ESI-MS to track real-time changes in the reaction mixture composition proved cobalt(II) was responsible for the undesired transformation. The occurrence of cobalt(II)-promoted hydrodehalogenation as a side reaction in this MCR had not been considered in previous mechanistic proposals and represents an important mechanistic consideration.


2019 ◽  
Vol 14 (23) ◽  
pp. 4074-4086 ◽  
Author(s):  
Anup Mandal ◽  
Suman Dana ◽  
Deepan Chowdhury ◽  
Mahiuddin Baidya

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