Can Accelerated Reactions in Droplets Guide Chemistry at Scale?

European Journal of Organic Chemistry

Volumn 2016, Issue 33, 2016, Pages 5480-5484

  Wleklinski, Michael ^a   Falcone, Caitlin E ^a   Loren, Bradley P ^a   Jaman, Zinia ^a   Iyer, Kiran ^a   Ewan, H Samuel ^a   Hyun, Seok Hee ^a   Thompson, David H ^a   Cooks, R Graham ^a  

^a PURDUE UNIVERSITY   (United States)

Author keywords

Flow chemistry; Kinetics; Leidenfrost effect; Mass spectrometry; Reaction acceleration

Indexed keywords

EID: 84995961462     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201601270     Document Type: Article

References (26)

1. X. Yan, R. M. Bain and R. G. Cooks, Angew. Chem. Int. Ed., 2016, 55, 12960–12972;
2. Angew. Chem., 2016, 128, 13152–13156
3. R. M. Bain, C. J. Pulliam and R. G. Cooks, Chem. Sci., 2015, 6, 397–401;
4. R. M. Bain, C. J. Pulliam, S. T. Ayrton, K. Bain and R. G. Cooks, Rapid Commun. Mass Spectrom., 2016, 30, 1875–1878.
5. J. K. Lee, S. Kim, H. G. Nam and R. N. Zare, Proc. Natl. Acad. Sci. USA, 2015, 112, 3898–3903;
6. R. M. Bain, C. J. Pulliam, S. A. Raab and R. G. Cooks, J. Chem. Educ., 2016, 93, 340–344;
7. Y. Li, X. Yan and R. G. Cooks, Angew. Chem. Int. Ed., 2016, 55, 3433–3437;
8. Angew. Chem., 2016, 128, 3494.
9. S. Banerjee and R. N. Zare, Angew. Chem. Int. Ed., 2015, 54, 14795–14799;
10. Angew. Chem., 2015, 127, 15008.
11. C. Josserand and S. T. Thoroddsen, Annual Rev. Fluid Mechanics, 2016, 48, 365–391.
12. R. M. Bain, C. J. Pulliam, F. Thery and R. G. Cooks, Angew. Chem. Int. Ed., 2016, 55, 10478–10482;
13. Angew. Chem., 2016, 128, 10634–10638.
14. S. Mascia, P. L. Heider, H. Zhang, R. Lakerveld, B. Benyahia, P. I. Barton, R. D. Braatz, C. L. Cooney, J. M. B. Evans, T. F. Jamison, K. F. Jensen, A. S. Myerson and B. L. Trout, Angew. Chem. Int. Ed., 2013, 52, 12359–12363;
15. Angew. Chem., 2013, 125, 12585.
16. A. Adamo, R. L. Beingessner, M. Behnam, J. Chen, T. F. Jamison, K. F. Jensen, J.-C. M. Monbaliu, A. S. Myerson, E. M. Revalor, D. R. Snead, T. Stelzer, N. Weeranoppanant, S. Y. Wong and P. Zhang, Science, 2016, 352, 61–67.
17. A. Buitrago Santanilla, E. L. Regalado, T. Pereira, M. Shevlin, K. Bateman, L.-C. Campeau, J. Schneeweis, S. Berritt, Z.-C. Shi, P. Nantermet, Y. Liu, R. Helmy, C. J. Welch, P. Vachal, I. W. Davies, T. Cernak and S. D. Dreher, Science, 2015, 347, 49–53.
18. A. G. Godfrey, T. Masquelin and H. Hemmerle, Drug Discovery Today, 2013, 18, 795–802.
19. H. Song, D. L. Chen and R. F. Ismagilov, Angew. Chem. Int. Ed., 2006, 45, 7336–7356;
20. Angew. Chem., 2006, 118, 7494;
21. K. Jähnisch, V. Hessel, H. Löwe and M. Baerns, Angew. Chem. Int. Ed., 2004, 43, 406–446;
22. Angew. Chem., 2004, 116, 410.
23. S. C. Gibson, C. S. Feigerle and K. D. Cook, Anal. Chem., 2014, 86, 464–472.
24. D. R. Snead and T. F. Jamison, Chem. Sci., 2013, 4, 2822–2827.
25. D. T. Snyder, C. J. Pulliam, Z. Ouyang and R. G. Cooks, Anal. Chem., 2016, 88, 2–29.
26. R. Abdelaziz, D. Disci-Zayed, M. K. Hedayati, J.-H. Pöhls, A. U. Zillohu, B. Erkartal, V. S. K. Chakravadhanula, V. Duppel, L. Kienle and M. Elbahri, Nat. Commun., 2013, 4, 2400.