ChemInform Abstract: Reductive Alkylation of Orthoformates by Organoaluminum Compounds.

ChemInform ◽  
2010 ◽  
Vol 33 (49) ◽  
pp. no-no
Author(s):  
O. S. Vostrikova ◽  
Ye. F. Dekhtayr ◽  
S. S. Zloysky
Synthesis ◽  
1984 ◽  
Vol 1984 (10) ◽  
pp. 831-832 ◽  
Author(s):  
J. Barluenga ◽  
L. Ferrera ◽  
C. Nájera ◽  
M. Yus
Keyword(s):  

Catalysts ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 39
Author(s):  
Lyudmila V. Parfenova ◽  
Pavel V. Kovyazin ◽  
Almira Kh. Bikmeeva ◽  
Eldar R. Palatov

The activity and chemoselectivity of the Cp2ZrCl2-XAlBui2 (X = H, Bui) and [Cp2ZrH2]2-ClAlEt2 catalytic systems activated by (Ph3C)[B(C6F5)4] or B(C6F5)3 were studied in reactions with 1-hexene. The activation of the systems by B(C6F5)3 resulted in the selective formation of head-to-tail alkene dimers in up to 93% yields. NMR studies of the reactions of Zr complexes with organoaluminum compounds (OACs) and boron activators showed the formation of Zr,Zr- and Zr,Al-hydride intermediates, for which diffusion coefficients, hydrodynamic radii, and volumes were estimated using the diffusion ordered spectroscopy DOSY. Bis-zirconium hydride clusters of type x[Cp2ZrH2∙Cp2ZrHCl∙ClAlR2]∙yRnAl(C6F5)3−n were found to be the key intermediates of alkene dimerization, whereas cationic Zr,Al-hydrides led to the formation of oligomers.


2016 ◽  
Vol 57 (8) ◽  
pp. 864-867 ◽  
Author(s):  
Eliana E. Kim ◽  
Evans O. Onyango ◽  
Jennifer R. Pace ◽  
Timothy M. Abbot ◽  
Liangfeng Fu ◽  
...  
Keyword(s):  

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