Continuous Flow Generation and Reactions of Anhydrous Diazomethane Using a Teflon AF-2400 Tube-in-Tube Reactor

2013 ◽  
Vol 15 (21) ◽  
pp. 5590-5593 ◽  
Author(s):  
Federica Mastronardi ◽  
Bernhard Gutmann ◽  
C. Oliver Kappe
ChemInform ◽  
2012 ◽  
Vol 43 (38) ◽  
pp. no-no
Author(s):  
Duncan L. Browne ◽  
Matthew O'Brien ◽  
Peter Koos ◽  
Philippa B. Cranwell ◽  
Anastasios Polyzos ◽  
...  

Synlett ◽  
2012 ◽  
Vol 23 (09) ◽  
pp. 1402-1406 ◽  
Author(s):  
Steven Ley ◽  
Duncan Browne ◽  
Matthew O'Brien ◽  
Peter Koos ◽  
Philippa Cranwell ◽  
...  

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.


ChemSusChem ◽  
2013 ◽  
Vol 7 (2) ◽  
pp. 536-542 ◽  
Author(s):  
Krzysztof Skowerski ◽  
Stefan J. Czarnocki ◽  
Paweł Knapkiewicz

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

2019 ◽  
Vol 4 (2) ◽  
pp. 346-350 ◽  
Author(s):  
Chengwen Xue ◽  
Jiesheng Li ◽  
Jin Ping Lee ◽  
Ping Zhang ◽  
Jie Wu

Aqueous ammonia was applied as the ammonia source in the continuous amination of aromatic and heteroaromatic halides assisted by a Teflon AF-2400 tube-in-tube reactor to generate densely substituted aryl/heteroaryl amines in high yields.


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.


Catalysts ◽  
2018 ◽  
Vol 8 (2) ◽  
pp. 58 ◽  
Author(s):  
Yang Bai ◽  
Nikolay Cherkasov ◽  
Steven Huband ◽  
David Walker ◽  
Richard Walton ◽  
...  

2015 ◽  
Vol 123 (1435) ◽  
pp. 101-105 ◽  
Author(s):  
Eiji FUJII ◽  
Koji KAWABATA ◽  
Yuki SHIROSAKI ◽  
Satoshi HAYAKAWA ◽  
Akiyoshi OSAKA

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