Multidentate Lewis acids: theoretical study of anion binding by organoboron macrocyclic hosts

1993 ◽  
Vol 115 (24) ◽  
pp. 11216-11221 ◽  
Author(s):  
Solomon Jacobson ◽  
Richard Pizer
2012 ◽  
Vol 116 (33) ◽  
pp. 8608-8614 ◽  
Author(s):  
Okuma Emile Kasende ◽  
Jules Tshishimbi Muya ◽  
Lies Broeckaert ◽  
Guido Maes ◽  
Paul Geerlings

Author(s):  
Santiago Camanyes ◽  
Feliu Maseras ◽  
Miquel Moreno ◽  
Agustí Lledós ◽  
José M. Lluch ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 32 (37) ◽  
pp. no-no
Author(s):  
Yun-Dong Wu ◽  
Di-Fei Wang ◽  
Jonathan L. Sessler

2004 ◽  
Vol 43 (2) ◽  
pp. 490-505 ◽  
Author(s):  
Maik Finze ◽  
Eduard Bernhardt ◽  
Manfred Zähres ◽  
Helge Willner

2005 ◽  
Vol 690 (11) ◽  
pp. 2725-2731 ◽  
Author(s):  
Natalie D. Coombs ◽  
Simon Aldridge ◽  
Gavin Wiltshire ◽  
Deborah L. Kays (née Coombs) ◽  
Christopher Bresner ◽  
...  
Keyword(s):  

2009 ◽  
Vol 87 (7) ◽  
pp. 1074-1080 ◽  
Author(s):  
Carles Acosta-Silva ◽  
Òscar González-Blanco ◽  
Vicenç Branchadell

The hetero-Diels–Alder reactions of butadiene with Fe(CO)3-coordinated formylbutadiene and formyltrimethylenemethane catalyzed by Lewis acids have been theoretically studied through density functional calculations. The results obtained show that, for the reaction with (formylbutadiene)Fe(CO)3, the kinetically most favourable product is the one corresponding to the attack of butadiene on the s-cis conformer of the formylbutadiene fragment when the reaction is catalyzed by BF3, and the one corresponding to the attack on the s-trans conformer when the catalyst is TiCl4. On the other hand, for the reaction with (formyltrimethylenemethane)Fe(CO)3 catalyzed by BF3, the product corresponding to the attack on the s-trans conformer is predicted to be favoured. These results have been interpreted through an energy decomposition analysis of the potential-energy barriers.


2007 ◽  
Vol 13 (2) ◽  
pp. 657-665 ◽  
Author(s):  
Chagit Denekamp ◽  
Kinga Suwinska ◽  
Hussein Salman ◽  
Yael Abraham ◽  
Yoav Eichen ◽  
...  

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