Selectivity engineering of the diazotization reaction in a continuous flow reactor

Reaction Chemistry and Engineering

Volumn 1, Issue 4, 2016, Pages 387-396

  Shukla, C A ^a   Kulkarni, A A ^a   Ranade, V V ^a  

^a NATIONAL CHEMICAL LABORATORY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 85044908083     PISSN: None     EISSN: 20589883     Source Type: Journal    
DOI: 10.1039/c5re00056d     Document Type: Article

References (44)

1. L. Kürti and B. Czakó, Strategic Applications of Named Reactions in Organic Synthesis: Background and Detailed Mechanisms, Elsevier Academic Press, 2005
2. M. R. Heinrich Chem.-Eur. J. 2009 15 820 833
3. F. Mo G. Dong Y. Zhang J. Wang Org. Biomol. Chem. 2013 11 1582 1593
4. R. Fortt R. C. Wootton A. J. de Mello Org. Process Res. Dev. 2003 7 762 768
5. D. F. DeTar, in Organic Reactions, John Wiley & Sons, Inc., 2004, ch. 7, pp. 409-462
6. Z.-Q. Yu Y.-W. Lv C.-M. Yu W.-K. Su Tetrahedron Lett. 2013 54 1261 1263
7. D. P. Hari B. Koenig Angew. Chem., Int. Ed. 2013 52 4734 4743
8. N. Chernyak S. L. Buchwald J. Am. Chem. Soc. 2012 134 12466 12469
9. V. G. Bhaya R. A. Joshi A. A. Kulkarni J. Flow Chem. 2014 4 211 216
10. A. Roglans A. Pla-Quintana M. Moreno-Manas Chem. Rev. 2006 106 4622 4643
11. S. Bhattacharya S. Majee R. Mukherjee S. Sengupta Synth. Commun. 1995 25 651 657
12. N. Oger M. d'Halluin E. Le Grognec F. O.-X. Felpin Org. Process Res. Dev. 2014 18 1786 1801
13. K. Meguro and T. Fujita, US Pat., 4687777, Takeda Chemical Industries, Ltd., 1987
14. H. Satoh, M. Komuro, K. Murakami and K. Awano, US Pat., 6706763B1, Kyorin Pharmaceutical Co., Ltd., 2004
15. G. J. Wells M. Tao K. A. Josef R. Bihovsky J. Med. Chem. 2001 44 3488 3503
16. R. C. Wedlich Chem. Eng. Prog. 2001 97 60 61
17. S. Partington S. Waldram Process Saf. Environ. Prot. 2002 80 33 39
18. UK Chemical Reaction Hazards Forum, http://www.crhf.org.uk/incident71.html, (accessed June 2015))
19. F. Stoessel, Thermal safety of chemical processes: risk assessment and process design, John Wiley & Sons, 2008
20. J. M. Sullivan J. Chem. Educ. 1971 48 419
21. R. W. Missen, R. W. Missen, C. A. Mims and B. A. Saville, Introduction to chemical reaction engineering and kinetics, Wiley, 1999
22. L. Malet-Sanz J. Madrzak S. V. Ley I. R. Baxendale Org. Biomol. Chem. 2010 8 5324 5332
23. M. Chen S. L. Buchwald Angew. Chem., Int. Ed. 2013 52 4247 4250
24. K. S. Nalivela M. Tilley M. A. McGuire M. G. Organ Chem.-Eur. J. 2014 20 6603 6607
25. D. X. Hu M. O'Brien S. V. Ley Org. Lett. 2012 14 4246 4249
26. N. Zaborenko E. R. Murphy J. G. Kralj K. F. Jensen Ind. Eng. Chem. Res. 2010 49 4132 4139
27. N. Oger E. Le. Grognec F. Felpin Org. Chem. Front. 2015 2 590 614
28. M. Okano Y. Ogata J. Am. Chem. Soc. 1953 75 5175 5177
29. L. Zolton, Ph.D.Thesis, University of Arezona, 1962
30. E. Moelwyn-Hughes P. Johnson Trans. Faraday Soc. 1940 36 948 956
31. O. Levenspiel, Chemical reaction engineering, Wiley, 1972
32. L. T. Fan Y. K. Ahn Ind. Eng. Chem. Process Des. Dev. 1962 1 190 195
33. K. D. Nagy B. Shen T. F. Jamison K. F. Jensen Org. Process Res. Dev. 2012 16 976 981
34. J. H. Lienhard, A heat transfer textbook, Courier Corporation, 2013
35. S. S. Elnashaie and F. Uhlig, Numerical Techniques for Chemical and Biological Engineers Using MATLAB®: A Simple Bifurcation Approach, Springer Science & Business Media, 2007
36. M. L. Kesler, US Pat., 2827449, American Cyanamid Company, 1958
37. H. Zollinger, in Diazo Chemistry I: Aromatic and Heteroaromatic Compounds, 1994, ch. 2, pp. 11-37
38. T. Norris C. Bezze S. Z. Franz M. Stivanello Org. Process Res. Dev. 2008 13 354 357
39. E. L. Paul Chem. Eng. Sci. 1988 43 1773 1782
40. M. Sharma V. S. Reddy A. A. Kulkarni Ind. Eng. Chem. Res. 2014 53 1916 1923
41. V. V. Ranade M. K. Sharma A. A. Kulkarni Chem. Eng. J. 2015 278 454 468
42. E. L. Paul, V. Atiemo-Obeng and S. M. Kresta, Handbook of Industrial Mixing: Science and Practice, John Wiley & Sons, 2003
43. P. Mavros Miner. Eng. 1992 5 1053 1060
44. M. Ityokumbul N. Kosaric W. Bulani Chem. Eng. Sci. 1988 43 2457 2462