scholarly journals Efficient Synthesis of Enantiopure β-Amino-γ-Keto Acids from L-Homoserine.

ChemInform ◽  
2003 ◽  
Vol 34 (40) ◽  
Author(s):  
Anil K. Sharma ◽  
Paul J. Hergenrother
ACS Catalysis ◽  
2020 ◽  
Vol 10 (17) ◽  
pp. 9994-10004
Author(s):  
Wei Song ◽  
Xin Xu ◽  
Cong Gao ◽  
Yuxuan Zhang ◽  
Jing Wu ◽  
...  

2017 ◽  
Vol 13 ◽  
pp. 1425-1429 ◽  
Author(s):  
Lina Jia ◽  
Fuzhong Han

Background: Phthalides are privileged constituents of numerous pharmaceuticals, natural products and agrochemicals and exhibit several biological and therapeutic activities. Therefore, the development of new, facile, and sustainable strategies for the construction of these moieties is highly desired. Results: A broad substrate scope for β-keto acids was found to be strongly compatible with this catalytic process, affording a wide variety of 3-substituted phthalides in good to excellent yields. Conclusion: A concise and efficient synthesis strategy of 3-substituted phthalides from 2-formylbenzoic acid and β-keto acids via a catalytic one-pot cascade reaction in glycerol has been accomplished.


Catalysts ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 1054
Author(s):  
Xiao-Qiang Hu ◽  
Zi-Kui Liu ◽  
Wen-Jing Xiao

Visible light photocatalytic radical carbonylation has been established as a robust tool for the efficient synthesis of carbonyl-containing compounds. Acyl radicals serve as the key intermediates in these useful transformations and can be generated from the addition of alkyl or aryl radicals to carbon monoxide (CO) or various acyl radical precursors such as aldehydes, carboxylic acids, anhydrides, acyl chlorides or α-keto acids. In this review, we aim to summarize the impact of visible light-induced acyl radical carbonylation reactions on the synthesis of oxygen and nitrogen heterocycles. The discussion is mainly categorized based on different types of acyl radical precursors.


2003 ◽  
Vol 5 (12) ◽  
pp. 2107-2109 ◽  
Author(s):  
Anil K. Sharma ◽  
Paul J. Hergenrother

2017 ◽  
Vol 4 (6) ◽  
pp. 1029-1033 ◽  
Author(s):  
Wenbin Mao ◽  
Chen Zhu

A general and efficient approach to highly substituted butenolides through the annulation of keto acids and terminal alkynes is described.


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