Enantioselective Mannich Reaction of β-Keto Esters with Aromatic and Aliphatic Imines Using a Cooperatively Assisted Bifunctional Catalyst

2014 ◽  
Vol 16 (19) ◽  
pp. 5152-5155 ◽  
Author(s):  
Antti J. Neuvonen ◽  
Petri M. Pihko
2019 ◽  
Vol 33 (7) ◽  
Author(s):  
Yunyun Wang ◽  
Yajun Jian ◽  
Ya Wu ◽  
Huaming Sun ◽  
Guofang Zhang ◽  
...  

2017 ◽  
Vol 8 (2) ◽  
pp. 1238-1242 ◽  
Author(s):  
Xiangjin Lian ◽  
Lili Lin ◽  
Kai Fu ◽  
Baiwei Ma ◽  
Xiaohua Liu ◽  
...  

An efficient asymmetric Mannich-type reaction between α-tetralone-derived β-keto esters/amides and 1,3,5-triaryl-1,3,5-triazinanes was realized catalyzed by chiral N,N'–dioxide-Ni(ii)/Mg(ii) complexes.


2012 ◽  
pp. 1
Author(s):  
K. Hof ◽  
K. M. Lippert ◽  
P. R. Schreiner
Keyword(s):  

Synlett ◽  
2017 ◽  
Vol 28 (11) ◽  
pp. 1300-1304 ◽  
Author(s):  
Jiean Chen ◽  
Yong Huang ◽  
Fei Wang

An enantioselective [3+2] cyclization is reported for the construction of a chiral oxazoline skeleton in moderate yield and up to 97% ee. The reactivity and stereochemical discrimination originate from the noncovalent interaction and orientation of a bifunctional catalyst. The novel combination of an α-keto ester and an α-isocyanoacetate establishes an oxazoline which could be a potential chiral ligand for metal-mediated catalysis, and also could be easily converted into an optically active β-hydroxy-α-amino acid.


2006 ◽  
Author(s):  
Dominique Cahard ◽  
Jun-An Ma ◽  
Vitaliy Petrik
Keyword(s):  

2020 ◽  
Vol 24 ◽  
Author(s):  
Ilnaz Baagheri ◽  
Leila Mohammadi ◽  
Vahideh Zadsirjan ◽  
Majid M. Heravi

The article has been withdrawn at the request of editor of the journal Current Organic Chemistry: Bentham Science apologizes to the readers of the journal for any inconvenience this may have caused. The Bentham Editorial Policy on Article The Bentham Editorial Policy on Article Withdrawal can be found at https://benthamscience.com/editorial-policies-main.php BENTHAM SCIENCE DISCLAIMER: It is a condition of publication that manuscripts submitted to this journal have not been published and will not be simultaneously submitted or published elsewhere. Furthermore, any data, illustration, structure or table that has been published elsewhere must be reported, and copyright permission for reproduction must be obtained. Plagiarism is strictly forbidden, and by submitting the article for publication the authors agree that the publishers have the legal right to take appropriate action against the authors, if plagiarism or fabricated information is discovered. By submitting a manuscript, the authors agree that the copyright of their article is transferred to the publishers if and when the article is accepted for publication.


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