Theoretical Studies on the Diastereoselectivity in the Lewis Acid Catalyzed CarbonylEne Reaction: A Fundamental Role of Electrostatic Interaction

2002 ◽  
Vol 85 (12) ◽  
pp. 4264-4271 ◽  
Author(s):  
Masahiro Yamanaka ◽  
Koichi Mikami
2021 ◽  
pp. 1-11
Author(s):  
Debasree Chanda ◽  
Gangothri M. Venkataswamy ◽  
Lagamawwa V. Hipparagi ◽  
Nanishankar V. Harohally

ChemInform ◽  
2011 ◽  
Vol 42 (18) ◽  
pp. no-no
Author(s):  
Bo Han ◽  
You-Cai Xiao ◽  
Yuan Yao ◽  
Ying-Chun Chen

2010 ◽  
Vol 122 (52) ◽  
pp. 10387-10389 ◽  
Author(s):  
Bo Han ◽  
You-Cai Xiao ◽  
Yuan Yao ◽  
Ying-Chun Chen

2012 ◽  
Vol 77 (22) ◽  
pp. 10184-10193 ◽  
Author(s):  
Luciana M. Ramos ◽  
Adrian Y. Ponce de Leon y Tobio ◽  
Marcelo R. dos Santos ◽  
Heibbe C. B. de Oliveira ◽  
Alexandre F. Gomes ◽  
...  

1994 ◽  
Vol 71 (2) ◽  
pp. 231-232 ◽  
Author(s):  
Jill F. McLellan ◽  
Roy M. Mortier ◽  
Stefan T. Orszulik ◽  
R. Michael Paton

2011 ◽  
Vol 76 (17) ◽  
pp. 6997-7004 ◽  
Author(s):  
Filipe J. S. Duarte ◽  
Snezhana M. Bakalova ◽  
Eurico J. Cabrita ◽  
A. Gil Santos

Author(s):  
Axel G Griesbeck ◽  
Lars-Oliver Höinck ◽  
Jörg M Neudörfl

Cycloalkanones were utilized in the Lewis acid catalyzed peroxyacetalization of ß-hydroperoxy homoallylic alcohols (prepared by the ene reaction of the allylic alcohols mesitylol and methyl 4-hydroxytiglate, respectively, with singlet oxygen) to give spiroannulated 1,2,4-trioxanes 5a–5e and 9a–9e, respectively. A second series of 3-arylated trioxanes 10a–10h, that are available from the hydroperoxy alcohol 4 and benzaldehyde derivatives, was investigated by X-ray crystallography.


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