ChemInform Abstract: The Asymmetric Addition of Trimethylsilyl Cyanide to Ketones Catalyzed by a Bimetallic, Chiral (Salen)titanium Complex.

ChemInform ◽  
2010 ◽  
Vol 31 (8) ◽  
pp. no-no
Author(s):  
Yuri N. Belokon ◽  
Brendan Green ◽  
Nicolai S Ikonnikov ◽  
Michael North ◽  
Vitali I. Tararov
1999 ◽  
Vol 40 (46) ◽  
pp. 8147-8150 ◽  
Author(s):  
Yuri N Belokon ◽  
Brendan Green ◽  
Nicolai S Ikonnikov ◽  
Michael North ◽  
Vitali I Tararov

2005 ◽  
Vol 46 (13) ◽  
pp. 2223-2226 ◽  
Author(s):  
Zi-Bo Li ◽  
Amaresh R. Rajaram ◽  
Nattawan Decharin ◽  
Ying-Chuan Qin ◽  
Lin Pu

ChemInform ◽  
2010 ◽  
Vol 28 (39) ◽  
pp. no-no
Author(s):  
YU. BELOKON' ◽  
M. FLEGO ◽  
N. IKONNIKOV ◽  
M. MOSCALENKO ◽  
M. NORTH ◽  
...  

1998 ◽  
pp. 387-388 ◽  
Author(s):  
Michael North ◽  
Charles Orizu ◽  
Vitali I. Tararov ◽  
Nicolai S. Ikonnikov ◽  
Yuri N. Belokon ◽  
...  

2006 ◽  
Vol 348 (4-5) ◽  
pp. 506-514 ◽  
Author(s):  
Zhaoqing Xu ◽  
Li Lin ◽  
Jiangke Xu ◽  
Wenjin Yan ◽  
Rui Wang

Author(s):  
Yuri N. Belokon’ ◽  
Brendan Green ◽  
Nicolai S. Ikonnikov ◽  
Vladimir S. Larichev ◽  
Boris V. Lokshin ◽  
...  

2020 ◽  
Author(s):  
Zhipeng Zhang ◽  
Zheng Wang ◽  
Kuiling Ding

Enantioselective addition of trimethylsilyl cyanide (TMSCN) to aldehydes is one of the most extensively studied organic reactions in asymmetric catalysis. Herein, we report our intensive kinetic investigation on the asymmetric addition of TMSCN to benzaldehyde, catalyzed by a covalently bridged dinuclear (salen)titanium complex <b>2</b>, which has been one of the most efficient artificial chiral catalysts reported so far for this reaction. It was found that the method of initial rates for kinetic investigation is not appropriate in this case because of the presence of a significant <a></a><a>incubation </a>period in the catalysis, while the method of progress rates proved to be more reliable and efficient for judging the kinetic orders of this catalytic system. The kinetic results revealed that <a>the reaction follows first order with respect to the catalyst</a> and is nearly independent of concentrations of both benzaldehyde and TMSCN<a>. A detailed catalytic mechanism for cyanosilylation of benzaldehyde in the presence of <b>2</b> was proposed, wherein the key active dinuclear species works in a cooperative manner for dual activation of both reactants.</a>


1992 ◽  
Vol 114 (21) ◽  
pp. 7969-7975 ◽  
Author(s):  
Hideaki Nitta ◽  
Donghai Yu ◽  
Masanobu Kudo ◽  
Atsunori Mori ◽  
Shohei Inoue

ChemInform ◽  
2005 ◽  
Vol 36 (29) ◽  
Author(s):  
Zi-Bo Li ◽  
Amaresh R. Rajaram ◽  
Nattawan Decharin ◽  
Ying-Chuan Qin ◽  
Lin Pu

ChemInform ◽  
2010 ◽  
Vol 29 (22) ◽  
pp. no-no
Author(s):  
V. I. TARAROV ◽  
D. E. HIBBS ◽  
M. B. HURSTHOUSE ◽  
N. S. IKONNIKOV ◽  
K. M. A. MALIK ◽  
...  

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