ChemInform Abstract: The Asymmetric Synthesis of β-Lactam Antibiotics. Part 1. Application of Chiral Oxazolidones in the Staudinger Reaction. The Asymmetric Synthesis of β-Lactam Antibiotics. Part 2. The First Enantioselective Synthesis of the Carbacephal

1985 ◽  
Vol 16 (50) ◽  
Author(s):  
D. A. EVANS ◽  
E. B. SJOGREN
Synlett ◽  
2021 ◽  
Author(s):  
Memg Wang ◽  
Changxu Zhong ◽  
Ping Lu

Enantioselective synthesis of cyclobutane derivatives is still a challenging topic in asymmetric synthesis. [2+2]-Cycloaddition and skeleton rearrangement are two primary strategies to this end. Recently, functionalization of cyclobutanones and cyclobutenones, which are readily available via [2+2]-cycloadditions as prochiral substrates, has emerged as a powerful tool to access versatile four-membered ring compounds. Herein, we summarize some recent advances in these areas from our and other groups.


2016 ◽  
Vol 7 (2) ◽  
pp. 1205-1211 ◽  
Author(s):  
Ryo Shintani ◽  
Ryo Takano ◽  
Kyoko Nozaki

A rhodium-catalyzed regio- and enantioselective synthesis of silicon-stereogenic silicon-bridged arylpyridinones was developed. A reasonable catalytic cycle was also experimentally established.


Author(s):  
Alessandro Bongini ◽  
Mauro Panunzio ◽  
Giovanni Piersanti ◽  
Elisa Bandini ◽  
Giorgio Martelli ◽  
...  

2018 ◽  
pp. 1-123
Author(s):  
Aitor Landa ◽  
Antonia Mielgo ◽  
Mikel Oiarbide ◽  
Claudio Palomo

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