Lewis base-catalysed Mukaiyama–aldol reaction of trimethylsilyl enolates with aldehydes

2010 ◽  
Vol 2010 (5) ◽  
pp. 263-265 ◽  
Author(s):  
Xingxian Zhang ◽  
Junchen Shi ◽  
Shenghui Hu
2005 ◽  
Vol 34 (3) ◽  
pp. 420-421 ◽  
Author(s):  
Tomoo Mizugaki ◽  
Casey E. Hetrick ◽  
Makoto Murata ◽  
Kohki Ebitani ◽  
Michael D. Amiridis ◽  
...  

ChemInform ◽  
2005 ◽  
Vol 36 (34) ◽  
Author(s):  
Tomoo Mizugaki ◽  
Casey E. Hetrick ◽  
Makoto Murata ◽  
Kohki Ebitani ◽  
Michael D. Amiridis ◽  
...  

2020 ◽  
Author(s):  
Revannath L. Sutar ◽  
Nikita Erochok ◽  
Stefan Huber

A series of cationic monodentate and bidentate iodo(benz)­imidazolium-based halogen bond (XB) donors were employed as catalysts in a Mukaiyama aldol reaction. While 5 mol% of a monodentate variant showed noticeable activity, a <i>syn</i>-preorganized bidentate XB donor provided a strong performance even with 0.5 mol% loading. In contrast to the very active BAr<sup>F</sup><sub>4</sub> salts, PF<sub>6</sub> or OTf salts were either inactive or showed background reaction. Repetition experiments clearly ruled out a potential hidden catalysis by elemental iodine and demonstrated the stability of our catalyst over three consecutive cycles.


ChemInform ◽  
2013 ◽  
Vol 44 (22) ◽  
pp. no-no
Author(s):  
Hima Rani Kalita ◽  
Arun Jyoti Borah ◽  
Prodeep Phukan

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