Photo-Fries rearrangement in flow under aqueous micellar conditions

2020 ◽  
Vol 56 (98) ◽  
pp. 15470-15472
Author(s):  
Chia-Chen Chien ◽  
Shih-Chieh Kao ◽  
Chun-Jen Chen ◽  
Yen-Ku Wu

A combination of an aqueous micellar medium and a flow reactor provides a green approach for refining the classic photo-Fries rearrangement.

Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 3917
Author(s):  
Sofia Siciliano ◽  
Elena Cini ◽  
Maurizio Taddei ◽  
Giorgia Vinciarelli

The synthesis of 2-substituted indoles starting from the corresponding unprotected 2-alkynylanilines was made possible in 3% TPGS-750-M water using Pd(OAc)2 alone as the catalyst. The reaction was sensitive to the heating mode respect to the nature of the starting material as, in many cases, convectional heating was better than microwave dielectric heating. The MW (microwave) delivery mode had also an influence in the formation of by-products and, consequently, product yields. A tandem Sonogashira-cyclisation reaction was also accomplished using Pd(OAc)2/Xphos in the nanomicellar water environment.


RSC Advances ◽  
2015 ◽  
Vol 5 (57) ◽  
pp. 45740-45748 ◽  
Author(s):  
Emilia Iglesias ◽  
Isabel Brandariz

The reaction between captopril and phenylbenzoate yields S-benzoylcaptopril that is very stable in a carbonate buffer or in an aqueous micellar medium.


2011 ◽  
Vol 18 (3) ◽  
pp. 760-764 ◽  
Author(s):  
Lionel Laville ◽  
Clarence Charnay ◽  
Frédéric Lamaty ◽  
Jean Martinez ◽  
Evelina Colacino

2022 ◽  
Author(s):  
Bruce Howard Lipshutz ◽  
Vani Singhania ◽  
Margery Cortes-Clerget ◽  
Jade Dussart-Gautheret ◽  
Bhornrawin Akkachairin ◽  
...  

Esterification in an aqueous micellar medium is catalyzed by a commercially available lipase in the absence of any co-factors. The presence of only 2 wt % designer surfactant, TPGS-750-M, assists...


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