Highly Enantioselective Directsyn- andanti-Aldol Reactions of Dihydroxyacetones Catalyzed by Chiral Primary Amine Catalysts

2008 ◽  
Vol 10 (4) ◽  
pp. 653-656 ◽  
Author(s):  
Sanzhong Luo ◽  
Hui Xu ◽  
Long Zhang ◽  
Jiuyuan Li ◽  
Jin-Pei Cheng
ChemInform ◽  
2008 ◽  
Vol 39 (30) ◽  
Author(s):  
Sanzhong Luo ◽  
Hui Xu ◽  
Long Zhang ◽  
Jiuyuan Li ◽  
Jin-Pei Cheng

2020 ◽  
Author(s):  
Rémi Blieck ◽  
Sebastien Lemouzy ◽  
Marc Taillefer ◽  
Florian Monnier

A dual copper/enamine catalytic system is found to enable an intermolecular enantioselective α-addition of various carbonyl nucleophiles to allenamides. Secondary amine catalysts allowed the highly enantioselective addition of aldehydes, while using primary amine catalysts led to the enantioselective addition of ketoester nucleophiles. The process was found to be highly regio-, stereo- and enantio-selective and represented the first allene hydrofunctionalization using an synergistic catalysis involving copper


2011 ◽  
Vol 32 (6-8) ◽  
pp. 899-903 ◽  
Author(s):  
Qiang GAO ◽  
Yan LIU ◽  
Shengmei LU ◽  
Can LI

ChemInform ◽  
2010 ◽  
Vol 41 (35) ◽  
pp. no-no
Author(s):  
Sanzhong Luo ◽  
Pengxin Zhou ◽  
Jiuyuan Li ◽  
Jin-Pei Cheng

2015 ◽  
Vol 10 (10) ◽  
pp. 2112-2116 ◽  
Author(s):  
Shin A. Moteki ◽  
Hiroki Maruyama ◽  
Keiji Nakayama ◽  
Hai-Bei Li ◽  
Galina Petrova ◽  
...  

2020 ◽  
Author(s):  
Rémi Blieck ◽  
Sebastien Lemouzy ◽  
Marc Taillefer ◽  
Florian Monnier

A dual copper/enamine catalytic system is found to enable an intermolecular enantioselective α-addition of various carbonyl nucleophiles to allenamides. Secondary amine catalysts allowed the highly enantioselective addition of aldehydes, while using primary amine catalysts led to the enantioselective addition of ketoester nucleophiles. The process was found to be highly regio-, stereo- and enantio-selective and represented the first allene hydrofunctionalization using an synergistic catalysis involving copper


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