Catalysis of Mukaiyama Aldol Reactions by a Tricyclic Aluminum Alkoxide Lewis Acid

2009 ◽  
Vol 74 (15) ◽  
pp. 5417-5428 ◽  
Author(s):  
Steven M. Raders ◽  
John G. Verkade
2002 ◽  
pp. 2994-2995 ◽  
Author(s):  
Hui-Jing Li ◽  
Hong-Yu Tian ◽  
Yong-Jun Chen ◽  
Dong Wang ◽  
Chao-Jun Li

2006 ◽  
Vol 2006 (8) ◽  
pp. 1837-1844 ◽  
Author(s):  
Yukihiro Hiraiwa ◽  
Kazuaki Ishihara ◽  
Hisashi Yamamoto

ChemInform ◽  
2010 ◽  
Vol 30 (36) ◽  
pp. no-no
Author(s):  
Gloria Rassu ◽  
Paola Carta ◽  
Luigi Pinna ◽  
Lucia Battistini ◽  
Franca Zanardi ◽  
...  

Author(s):  
Gloria Rassu ◽  
Paola Carta ◽  
Luigi Pinna ◽  
Lucia Battistini ◽  
Franca Zanardi ◽  
...  

2012 ◽  
Vol 134 (36) ◽  
pp. 14973-14981 ◽  
Author(s):  
Joshua M. Lee ◽  
Paul Helquist ◽  
Olaf Wiest

ChemInform ◽  
2003 ◽  
Vol 34 (15) ◽  
Author(s):  
Hui-Jing Li ◽  
Hong-Yu Tian ◽  
Yong-Jun Chen ◽  
Dong Wang ◽  
Chao-Jun Li

Synthesis ◽  
2016 ◽  
Vol 48 (19) ◽  
pp. 3413-3419 ◽  
Author(s):  
Hannah Bartrum ◽  
Sébastien Carret ◽  
Jean-François Poisson

A mild method for the aldolization of N-sulfonylimidates was developed. The reaction proceeds in excellent diastereoselectivity to provide a range of useful β-hydroxyimidates in high yield. The innate reversibility of the reaction is suppressed by the use of a titanium complex as a Lewis acid.


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