Continuous-Flow Generation of Anhydrous Diazonium Species:  Monolithic Microfluidic Reactors for the Chemistry of Unstable Intermediates

2003 ◽  
Vol 7 (5) ◽  
pp. 762-768 ◽  
Author(s):  
Robin Fortt ◽  
Robert C. R. Wootton ◽  
Andrew J. de Mello
2021 ◽  
Vol 12 (4) ◽  
pp. 489-493
Author(s):  
Grace P. Ahlqvist ◽  
Eileen G. Burke ◽  
Jeremiah A. Johnson ◽  
Timothy F. Jamison

Herein we describe the development of a reactor for the continuous flow generation and use of dimethyldioxirane (DMDO) and its application to the low-level epoxidation of unsaturated polymers.


2015 ◽  
Vol 80 (9) ◽  
pp. 4590-4602 ◽  
Author(s):  
Carlos Eduardo M. Salvador ◽  
Bartholomäus Pieber ◽  
Philipp M. Neu ◽  
Ana Torvisco ◽  
Carlos Kleber Z. Andrade ◽  
...  

Synlett ◽  
2020 ◽  
Vol 31 (19) ◽  
pp. 1899-1902
Author(s):  
Jun-ichi Yoshida ◽  
Heejin Kim ◽  
Hyune-Jea Lee ◽  
Daiki Torii ◽  
Yongju Jeon

The isothiocyanate (NCS) group is an attractive functional group in the field of organic and pharmaceutical chemistry. It can be transformed into other heteroatomic functional groups. It usually acts as the inductive group of biological activity and has also been traditionally used as the fluorescent-labeling reagent. However, it is not compatible with strong bases. When the NCS group is at para position in halobenzenes, it generally undergoes nucleophilic additions upon reaction with strong bases. To the best of our knowledge, there is currently no general methodology for the formation and reactions of NCS-functionalized aryllithiums for meta and para substituents. Herein, we report the continuous-flow generation of NCS-substituted aryllithiums from the corresponding haloarenes via a selective halogen–lithium exchange reaction and its reaction with various electrophiles to yield NCS-containing products. We also achieved an integrated synthesis through sequential reactions of the NCS-containing compounds with additional nucleophiles using the continuous-flow reactors.


2013 ◽  
Vol 15 (21) ◽  
pp. 5590-5593 ◽  
Author(s):  
Federica Mastronardi ◽  
Bernhard Gutmann ◽  
C. Oliver Kappe

2021 ◽  
Author(s):  
Marco P. Cardoso Marques ◽  
Alvaro Lorente-Arevalo ◽  
Juan M. Bolivar

Tetrahedron ◽  
2013 ◽  
Vol 69 (10) ◽  
pp. 2276-2282 ◽  
Author(s):  
Hannah E. Bartrum ◽  
David C. Blakemore ◽  
Christopher J. Moody ◽  
Christopher J. Hayes

2020 ◽  
Vol 22 (19) ◽  
pp. 7537-7541
Author(s):  
Timo von Keutz ◽  
David Cantillo ◽  
C. Oliver Kappe

2011 ◽  
Vol 17 (35) ◽  
pp. 9586-9589 ◽  
Author(s):  
Hannah E. Bartrum ◽  
David C. Blakemore ◽  
Christopher J. Moody ◽  
Christopher J. Hayes

2017 ◽  
Vol 2 (6) ◽  
pp. 896-907 ◽  
Author(s):  
Mariana C. F. C. B. Damião ◽  
Renan Galaverna ◽  
Alan P. Kozikowski ◽  
James Eubanks ◽  
Julio C. Pastre

An integrated continuous flow process for the synthesis of 3-thio-1,2,4-triazoles is reported. A small library of 18 compounds was prepared in just 48 minutes of residence time in moderate to excellent yields.


2020 ◽  
Vol 247 ◽  
pp. 116723 ◽  
Author(s):  
Zheng-Tian Xie ◽  
Taka-Aki Asoh ◽  
Yuta Uetake ◽  
Hidehiro Sakurai ◽  
Hiroshi Uyama

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