scholarly journals The Effect of the Catalyst on the Selectivity of the Heterogeneous 1,4-addition of Organomagnesium Compounds to Chalcone

Author(s):  
Kinga Juhász ◽  
Zoltán Hell

The conjugate addition in the presence of a catalytic amount of copper is a widely used method for the formation of a C-C bond. However, mostly homogeneous catalysts and/or homogeneous ligands are used in these type of reactions. Previously we reported the heterogeneous catalytic 1,4-addition of organomagnesium compounds to chalcones in the presence of Cu(II) on 4Å molecular sieve support. In this study various heterogeneous supported catalysts were tested in the 1,4-addition reaction, such as La(III), Ti(IV), In(III), Co(II) and Ni(II) on 4Å molecular sieve support. Using the Ti(IV)-4A the desired products could be obtained in excellent yields and no 1,2-addition by-product could be detected. Therefore the reusability of the catalyst was tested in a second reaction. It was found, that the Ti(IV)-4A cannot be reused in this type of reaction, due to significant loss of selectivity. In the second experiment a considerable amount of the 1,2-addition product was formed. Thus, the Cu(II)-4A is a suitable catalyst for the heterogeneous 1,4-addition of organomagnesium compounds to chalcones, as described in our previous work.

ChemInform ◽  
2005 ◽  
Vol 36 (44) ◽  
Author(s):  
A. Alexakis

ChemInform ◽  
2013 ◽  
Vol 44 (22) ◽  
pp. no-no
Author(s):  
Alyson E. Garst ◽  
Alexandra D. Badiceanu ◽  
Kristine A. Nolin

1986 ◽  
Vol 27 (9) ◽  
pp. 1047-1050 ◽  
Author(s):  
A. Alexakis ◽  
J. Berlan ◽  
Y. Besace

Synlett ◽  
2018 ◽  
Vol 29 (09) ◽  
pp. 1203-1206 ◽  
Author(s):  
Hyoungsu Kim ◽  
Hosam Choi ◽  
Kiyoun Lee

A concise total synthesis of (±)-mesembrine has been successfully accomplished in seven steps and 24% overall yield from commercially available 3-ethoxy-2-cyclohexen-1-one. Central to the assembly of the skeleton of mesembrine are a Johnson–Claisen rearrangement for the formation of the benzylic quaternary stereocenter and direct allylic oxidation to generate the substrate for the amidation/transannular aza-conjugate addition reaction.


2018 ◽  
Vol 5 (1) ◽  
pp. 18-31
Author(s):  
Seetaram Mohapatra ◽  
Nilofar Baral ◽  
Nilima Priyadarsini Mishra ◽  
Pravati Panda ◽  
Sabita Nayak

Introduction: Aza-Michael addition is an important reaction for carbon-nitrogen bond formation in synthetic organic chemistry. Expalantion: Conjugate addition of imidazole to α,β-unsaturated carbonyl/cyano compounds provides significant numbers of the biologically and synthetically interesting products, such as β-amino acids and β-lactams, which have attracted great attention for their use as key intermediates of anticancer agents, antibiotics and other drugs. Conclusion: This review addresses most significant method for the synthesis of N-substituted imidazole derivatives following Michael addition reaction of imidazole to α,β-unsaturated carbonyl/cyano compounds using ionic liquid/base/acid/enzyme as catalysts from year 2007-2017.


2012 ◽  
Vol 77 (7) ◽  
pp. 3557-3562 ◽  
Author(s):  
Yan-li Xu ◽  
Ying-ming Pan ◽  
Pei Liu ◽  
Heng-shan Wang ◽  
Xiao-yan Tian ◽  
...  

2020 ◽  
Vol 11 (1) ◽  
pp. 257-263 ◽  
Author(s):  
Gianluca Casotti ◽  
Gianluca Ciancaleoni ◽  
Filippo Lipparini ◽  
Chiara Nieri ◽  
Anna Iuliano

The reaction mechanism of a new conjugate addition reaction of organozinc halides to enones is disclosed by a combined experimental/computational study.


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