ChemInform Abstract: Highly Efficient Asymmetric anti-Mannich Reactions of Carbonyl Compounds with N-Carbamoyl Imines Catalyzed by Amino-Thiourea Organocatalysts.

ChemInform ◽  
2012 ◽  
Vol 43 (38) ◽  
pp. no-no
Author(s):  
Jiuzhi Gao ◽  
Yongming Chuan ◽  
Jiali Li ◽  
Fang Xie ◽  
Yungui Peng
2019 ◽  
Vol 55 (2) ◽  
pp. 179-181 ◽  
Author(s):  
Jorge Mendes-Burak ◽  
Behnaz Ghaffari ◽  
Christophe Copéret

Silica-supported copper nanoparticles prepared via surface organometallic chemistry are highly efficient for the selective hydrogenation of various α,β-unsaturated carbonyl compounds yielding the corresponding saturated esters, ketones, and aldehydes in the absence of additives.


Synlett ◽  
2019 ◽  
Vol 30 (15) ◽  
pp. 1810-1814 ◽  
Author(s):  
Enoch A. Mensah ◽  
Shawn D. Green ◽  
Jesse West ◽  
Tyler Kindoll ◽  
Brenda Lazaro-Martinez

The development of a new, highly efficient, and simple method for masking carbonyl groups as acetals and ketals is described. This methodology relies on the nature of the palladium catalyst to direct the acetalization/ketalization reaction. This new protocol is mild and proceed with a very low catalyst loading at ambient temperatures. The method has been extended to a wide variety of different carbonyl compounds with various steric encumbrances to form the corresponding acetals and ketals in excellent yields.


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