Domino Michael/Michael reaction catalyzed by switchable modularly designed organocatalysts

2022 ◽  
Author(s):  
Ramarao Parella ◽  
Satish Jakkampudi ◽  
Pranjal Bora ◽  
Nagaraju Sakkani ◽  
John C.-G. Zhao
Keyword(s):  
Michael Reaction

Both the enamine and iminium catalysis of the MDOs are switchable. Upon switching on both catalytic modes, the MDOs were used for catalyzing the domino Michael/Michael reaction between (E)-7-aryl-7-oxohept-5-enals and trans-cinnamaldehydes.

Phenolic Michael Reaction Acceptors: Combined Direct and Indirect Antioxidant Defenses Against Electrophiles and Oxidants

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

ChemInform Abstract: A Short Synthesis of (.+-.)-Ricciocarpin a Using Intramolecular Reductive Michael Reaction.

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

Sterically hindered 1,3-diketones in the Michael reaction

1996 ◽  
Vol 45 (1) ◽  
pp. 137-139
Author(s):  
I. E. Sokolov ◽  
A. S. Zanina ◽  
S. I. Shergina ◽  
M. S. Shvartsberg
Keyword(s):  
Michael Reaction ◽  
Sterically Hindered ◽  
The Michael Reaction

The Michael Reaction

2002 ◽  
Vol 79 (2) ◽  
pp. 264 ◽  
Author(s):  
Thomas Poon ◽  
Bradford P. Mundy ◽  
Thomas W. Shattuck
Keyword(s):  
Michael Reaction ◽  
The Michael Reaction

Tandem Nucleophilic Addition−Intramolecular Aza-Michael Reaction: Facile Synthesis of Chiral Fluorinated Isoindolines

2010 ◽  
Vol 12 (23) ◽  
pp. 5494-5497 ◽  
Author(s):  
Santos Fustero ◽  
Javier Moscardó ◽  
María Sánchez-Roselló ◽  
Elsa Rodríguez ◽  
Pablo Barrio
Keyword(s):  
Nucleophilic Addition ◽  
Michael Reaction ◽  
Facile Synthesis
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