ChemInform Abstract: Organocatalytic and Enantioselective Michael Reaction Between α-Nitroesters and Nitroalkenes. Syn/anti-Selectivity Control Using Catalysts with the Same Absolute Backbone Chirality.

ChemInform ◽  
2016 ◽  
Vol 47 (10) ◽  
pp. no-no
Author(s):  
Jose I. Martinez ◽  
Uxue Uria ◽  
Maria Muniz ◽  
Efraim Reyes ◽  
Luisa Carrillo ◽  
...  
2015 ◽  
Vol 11 ◽  
pp. 2577-2583 ◽  
Author(s):  
Jose I Martínez ◽  
Uxue Uria ◽  
Maria Muñiz ◽  
Efraím Reyes ◽  
Luisa Carrillo ◽  
...  

The asymmetric and catalytic Michael reaction between α-nitroesters and nitroalkenes has been studied in the presence of two bifunctional catalysts both containing the same absolute chirality at the carbon backbone. The reaction performed in similar conditions allows us to control the syn or anti selectivity of the Michael adduct obtaining good yields and high enantiocontrol in all cases.


2007 ◽  
Vol 3 (3) ◽  
pp. 261-268 ◽  
Author(s):  
A. Dinkova-Kostova ◽  
J. Cheah ◽  
A. Samouilov ◽  
J. Zweier ◽  
R. Bozak ◽  
...  

Author(s):  
Libo Yao ◽  
Yanbo Pan ◽  
Dezhen Wu ◽  
Jialu Li ◽  
Rongxuan Xie ◽  
...  

P-Modified In2O3 with composition regulation for approaching full-range selectivity control in CO2 hydrogenation to methanol and carbon monoxide.


ChemInform ◽  
2010 ◽  
Vol 29 (18) ◽  
pp. no-no
Author(s):  
K. TAKEDA ◽  
N. OHKAWA ◽  
K. HORI ◽  
T. KOIZUMI ◽  
E. YOSHII

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