Amino Acid Mediated Intramolecular Asymmetric Aldol Reaction to Construct a New Chiral Bicyclic Enedione Containing a Seven-Membered Ring:  Remarkable Inversion of Enantioselectivity Compared to the Six-Membered Ring Example

2007 ◽  
Vol 72 (1) ◽  
pp. 123-131 ◽  
Author(s):  
Takashi Nagamine ◽  
Kohei Inomata ◽  
Yasuyuki Endo ◽  
Leo A. Paquette
Tetrahedron ◽  
2016 ◽  
Vol 72 (13) ◽  
pp. 1706-1715 ◽  
Author(s):  
Pierre Milbeo ◽  
Kelly Maurent ◽  
Laure Moulat ◽  
Aurélien Lebrun ◽  
Claude Didierjean ◽  
...  

ChemInform ◽  
2016 ◽  
Vol 47 (28) ◽  
Author(s):  
Pierre Milbeo ◽  
Kelly Maurent ◽  
Laure Moulat ◽  
Aurelien Lebrun ◽  
Claude Didierjean ◽  
...  

RSC Advances ◽  
2014 ◽  
Vol 4 (46) ◽  
pp. 24311-24315 ◽  
Author(s):  
Sudipto Bhowmick ◽  
Sunita S. Kunte ◽  
Kartick C. Bhowmick

The catalytic efficacy of the smallest organocatalyst, l-proline hydrazide, prepared from a cheaply available natural amino acid, such as l-proline, was studied for the direct asymmetric aldol reaction of various ketones with aromatic aldehydes at room temperature in the presence of several acid additives.


Sign in / Sign up

Export Citation Format

Share Document