scholarly journals Construction of cyclic enones via gold-catalyzed oxygen transfer reactions

2011 ◽  
Vol 7 ◽  
pp. 606-614 ◽  
Author(s):  
Leping Liu ◽  
Bo Xu ◽  
Gerald B Hammond

During the last decade, gold-catalyzed reactions have become a tour de force in organic synthesis. Recently, the gold-, Brønsted acid- or Lewis acid-catalyzed oxygen transfer from carbonyl to carbon–carbon triple bond, the so-called alkyne–carbonyl metathesis, has attracted much attention because this atom economical transformation generates α,β-unsaturated carbonyl derivatives which are of great interest in synthetic organic chemistry. This mini-review focuses on the most recent achievements on gold-catalyzed oxygen transfer reactions of tethered alkynones, diynes or alkynyl epoxides to cyclic enones. The corresponding mechanisms for the transformations are also discussed.

2015 ◽  
Vol 729 ◽  
pp. 83-86 ◽  
Author(s):  
Dong Ming Lu ◽  
Zhi Jie Li ◽  
Feng Jiao Li ◽  
Qing Le Zeng

α-Hydroxy amides are a class of important intermediates in organic synthesis. It plays an important role in the field of science and medicine. However, the preparation methods of α-hydroxy amides are relatively few, and they are usually enzyme-or Lewis acid-catalyzed reactions. These types of methods are not ideal in operation, yield and/or stereoselectivity. We found a new way to synthesize α-hydroxy amides by transforming amino acids into α-hydroxyl acids, and then by amination of the α-hydroxy acids.


ChemInform ◽  
2010 ◽  
Vol 26 (46) ◽  
pp. no-no
Author(s):  
S. KOBAYASHI ◽  
I. HACHIYA

ChemInform ◽  
2010 ◽  
Vol 29 (44) ◽  
pp. no-no
Author(s):  
K. KOBAYASHI ◽  
S. MATOBA ◽  
S. IRISAWA ◽  
T. MATSUMOTO ◽  
O. MORIKAWA ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document