scholarly journals Diastereoselective synthesis of bis(α-aminophosphonates) by lipase catalytic promiscuity

2019 ◽  
Vol 43 (21) ◽  
pp. 8153-8159 ◽  
Author(s):  
Rim Aissa ◽  
Samia Guezane-Lakoud ◽  
Emilie Kolodziej ◽  
Martial Toffano ◽  
Louisa Aribi-Zouioueche

New bis(α-aminophosphonates) were directly prepared with high diastereoselectivity by lipase catalytic promiscuity in the presence of immobilized Candida antarctica lipase.

2016 ◽  
Vol 32 (3) ◽  
pp. 10-56
Author(s):  
A. V. SKLYARENKO ◽  
N. V. MEDVEDEVA ◽  
A. I. SIDORENKO ◽  
Y. HUANG ◽  
F. LI ◽  
...  
Keyword(s):  

2019 ◽  
Vol 23 (16) ◽  
pp. 1778-1788 ◽  
Author(s):  
Gurpreet Kaur ◽  
Arvind Singh ◽  
Kiran Bala ◽  
Mamta Devi ◽  
Anjana Kumari ◽  
...  

A simple, straightforward and efficient method has been developed for the synthesis of (E)-3-(arylimino)indolin-2-one derivatives and (E)-2-((4-methoxyphenyl)imino)- acenaphthylen-1(2H)-one. The synthesis of these biologically-significant scaffolds was achieved from the reactions of various substituted anilines and isatins or acenaphthaquinone, respectively, using commercially available, environmentally benign and naturally occurring organic acids such as mandelic acid or itaconic acid as catalyst in aqueous medium at room temperature. Mild reaction conditions, energy efficiency, good to excellent yields, environmentally benign conditions, easy isolation of products, no need of column chromatographic separation and the reusability of reaction media are some of the significant features of the present protocol.


2012 ◽  
Vol 9 (2) ◽  
pp. 81-88 ◽  
Author(s):  
Ervin Kovacs ◽  
Ferenc Farkas ◽  
Angelika Thurner ◽  
Aron Szollosy ◽  
Ferenc Faigl

2015 ◽  
Vol 4 (2) ◽  
pp. 87-99 ◽  
Author(s):  
Valerio Ferrario ◽  
Cynthia Ebert ◽  
Patrizia Nitti ◽  
Giuliana Pitacco ◽  
Lucia Gardossi

2018 ◽  
Vol 129 ◽  
pp. 12-24 ◽  
Author(s):  
Nathalia Saraiva Rios ◽  
Maisa Pessoa Pinheiro ◽  
Magno Luís Bezerra Lima ◽  
Denise Maria Guimarães Freire ◽  
Ivanildo José da Silva ◽  
...  

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