williamson ether synthesis
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2021 ◽  
Vol 75 (12) ◽  
pp. 1054-1057
Author(s):  
Gianni De Lucia ◽  
Massimo Varisco ◽  
Richard-Emmanuel Eastes ◽  
Christophe Allemann

Two experimental methods, the Nile Red dye extraction and the Williamson ether synthesis in biphasic conditions, were used to characterize the mixing performance of a new cheap impinging jet colliding mixer from Gjosa and to compare it to other commercial micromixers (Caterpillar CPMM-R300, T-mixer, LTF MR-MX and LTF MR-MS). The Nile Red method shows that the Caterpillar mixer is the best one. Excellent results are also achieved with two Gjosa mixers in series. These results are not reflected in the Williamson ether synthesis, where the best mixer is the Gjosa one.


Author(s):  
Aikaterini Diamanti ◽  
Zara Ganase ◽  
Eliana Grant ◽  
Alan Armstrong ◽  
Patrick M. Piccione ◽  
...  

New mechanistic understanding and the quantification of reaction kinetics shed light on the large impact of the solvent on selectivity.


2020 ◽  
Vol 27 (12) ◽  
pp. 14198-14206
Author(s):  
Yuyang Long ◽  
Zhiyuan Jin ◽  
Lijun Li ◽  
Mingxin Zhang ◽  
Lifang Hu ◽  
...  

2020 ◽  
Vol 97 (2) ◽  
pp. 578-581 ◽  
Author(s):  
Kasey L. Yearty ◽  
Ryan K. Maynard ◽  
Christina N. Cortes ◽  
Richard W. Morrison

2019 ◽  
Vol 14 (9) ◽  
pp. 1934578X1987621
Author(s):  
Masayoshi Yanagi ◽  
Noriyuki Uchida ◽  
Hiroki Hamada

Resveratrol derivatives containing a primary amine functional group were synthesized by an introduction of N-Boc-bromoethylamine to resveratrol using Williamson ether synthesis and subsequent deprotection of the Boc group with trifluoroacetic acid. After conjugation of fluorescent NBD-F or rhodamine B with isothiocyanate (Rhd B-ITC) using the amine group, resveratrols modified with NBD or Rhd B (Resveratrol-NBD and Resveratrol-Rhd B, respectively) were successfully obtained.


2017 ◽  
Vol 70 (5) ◽  
pp. 588 ◽  
Author(s):  
Jacob Whittaker ◽  
Suresh Moorthy ◽  
Jonathan Cremers ◽  
Jason R. Price ◽  
John C. McMurtrie ◽  
...  

The synthesis and characterisation of two 28-membered, 2,2′-bipyridine-containing macrocycles in high yield is reported. The first imine-containing macrocycle was formed via a Williamson ether synthesis and showed no evidence of higher oligomer formation. Reduction of the imines with sodium borohydride produced the second macrocycle quantitatively.


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