Amino Alcohol Catalyzed Direct Asymmetric Aldol Reactions. Enantioselective Synthesis of anti-α-Fluoro-β-hydroxy Ketones.

ChemInform ◽  
2004 ◽  
Vol 35 (44) ◽  
Author(s):  
Guofu Zhong ◽  
Junhua Fan ◽  
Carlos F. III Barbas
Chirality ◽  
2012 ◽  
Vol 25 (2) ◽  
pp. 119-125 ◽  
Author(s):  
Afroditi Pinaka ◽  
Georgios C. Vougioukalakis ◽  
Dimitra Dimotikali ◽  
Elina Yannakopoulou ◽  
Bezhan Chankvetadze ◽  
...  

2022 ◽  
Vol 09 ◽  
Author(s):  
Rubina Shajahan ◽  
Rithwik Sarang ◽  
Anas Saithalavi

The use of proline-based organocatalysts has acquired significant importance in organic synthesis, especially in enantioselective synthesis. Proline and its derivatives are proven to be quite effective chiral organocatalysts for a variety of transformations including the aldol reaction, which is considered as one of the important C-C bond forming reactions in organic synthesis. The use of chiral organocatalysts has several advantages over its metal-mediated analogues. Subsequently, a large number of highly efficient proline-based organocatalysts including polymer-supported chiral analogues have been identified for aldol reaction. The use of polymer-supported organocatalysts exhibited remarkable stability under the reaction conditions and offered the best results particularly in terms of its recyclability and reusability. These potential benefits along with its economic and green chemistry advantages have led to the search for many polymer-supported proline catalysts. In this review, recent developments in exploring various polymer immobilized proline-based chiral organocatalysts for asymmetric aldol reactions are described.


1994 ◽  
Vol 67 (6) ◽  
pp. 1708-1716 ◽  
Author(s):  
Teruaki Mukaiyama ◽  
Isamu Shiina ◽  
Hiromi Uchiro ◽  
Shu Kobayashi

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