l-Proline supported on ionic liquid-modified magnetic nanoparticles as a highly efficient and reusable organocatalyst for direct asymmetric aldol reaction in water

2013 ◽  
Vol 15 (9) ◽  
pp. 2422 ◽  
Author(s):  
Yu Kong ◽  
Rong Tan ◽  
Lili Zhao ◽  
Donghong Yin
Keyword(s):  
Ionic Liquid ◽  
Magnetic Nanoparticles ◽  
Aldol Reaction ◽  
Asymmetric Aldol ◽  
Highly Efficient ◽  
Asymmetric Aldol Reaction ◽  
Modified Magnetic Nanoparticles ◽  
Reaction In Water

Enhanced Activity and Stereoselectivity of Polystyrene-Supported Proline-Based Organic Catalysts for Direct Asymmetric Aldol Reaction in Water

2009 ◽  
Vol 2009 (31) ◽  
pp. 5437-5444 ◽  
Author(s):  
Michelangelo Gruttadauria ◽  
Anna Maria Pia Salvo ◽  
Francesco Giacalone ◽  
Paola Agrigento ◽  
Renato Noto
Keyword(s):  
Aldol Reaction ◽  
Asymmetric Aldol ◽  
Enhanced Activity ◽  
Asymmetric Aldol Reaction ◽  
Reaction In Water ◽  
Organic Catalysts

scholarly journals Organocatalytic Asymmetric Aldol Reaction of Arylglyoxals and Hydroxyacetone: Enantioselective Synthesis of 2,3-Dihydroxy-1,4-diones

Molecules ◽  
2020 ◽  
Vol 25 (3) ◽  
pp. 648
Author(s):  
Yu-Hao Zhou ◽  
Yu-Zu Zhang ◽  
Zhu-Lian Wu ◽  
Tian Cai ◽  
Wei Wen ◽  
...  
Keyword(s):  
Primary Amine ◽  
Aldol Reaction ◽  
Enantioselective Synthesis ◽  
Asymmetric Aldol ◽  
Highly Efficient ◽  
Asymmetric Aldol Reaction ◽  
Aldol Addition ◽  
High Yields

A highly efficient quinine-derived primary-amine-catalyzed asymmetric aldol addition of hydroxyacetone to arylglyoxals is described. Structurally diverse anti-2,3-dihydroxy-1,4-diones were generated in high yields, with good diastereoselectivities and enantioselectivities.

Recycling Chiral Organocatalyst (4S)-Phenoxy-(S)-proline for Direct Asymmetric Aldol Reaction in Ionic Liquid (bmim)PF6

2005 ◽  
Vol 23 (5) ◽  
pp. 634-636 ◽  
Author(s):  
Liu Yan-Hua ◽  
Zhang Ya-Wen ◽  
Ding Yi-Ping ◽  
Shen Zong-Xuan ◽  
Luo Xiao-Qing
Keyword(s):  
Ionic Liquid ◽  
Aldol Reaction ◽  
Asymmetric Aldol ◽  
Asymmetric Aldol Reaction

ChemInform Abstract: Highly Efficient Asymmetric Aldol Reaction in Brine Using a Fluorous Sulfonamide Organocatalyst.

ChemInform ◽  
2012 ◽  
Vol 43 (32) ◽  
pp. no-no
Author(s):  
Tsuyoshi Miura ◽  
Hikaru Kasuga ◽  
Kie Imai ◽  
Mariko Ina ◽  
Norihiro Tada ◽  
...  
Keyword(s):  
Aldol Reaction ◽  
Asymmetric Aldol ◽  
Highly Efficient ◽  
Asymmetric Aldol Reaction
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