The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
A Perspective on Continuous Flow Chemistry in the Pharmaceutical Industry
Open accessAbstract
Continuous flow manufacture is an innovative technology platform, which is gaining momentum within the pharmaceutical industry. The key advantages of continuous flow include faster and safer reactions, which can be more environmentally friendly, smaller footprint, better quality product, and critically, the ability to perform chemistry that is difficult or impossible to do in batch mode. Globally, significant efforts have been made to develop the manufacturing flexibility and robustness of processes used to produce chemicals in a continuous way, yet despite these scientific developments, a major challenge for industry is the established application of flow technology to commercially relevant examples. The identification of opportunities to apply flow solutions to current processes is also critical to the success of this new technology for pharmaceutical and fine chemical companies. This review highlights industrial hurdles and the importance of education and showcases recent (2018–2019) and relevant industrial examples where utilization of flow technology has been successfully performed.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Prier, C. K., Rankic, D. A., & MacMillan, D. W. C. (2013) · Chemical Reviews · doi:10.1021/cr300503r · Cited by 9,590
The Hitchhiker’s Guide to Flow Chemistry
Plutschack, M. B., Pieber, B., Gilmore, K., & Seeberger, P. H. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00183 · Cited by 1,995
Research works printed but not linked: 89
- 10.1002/anie.201409318 · DOI · Paper page
- 10.3762/bjoc.11.134 · DOI
- 10.1021/acs.oprd.5b00325 · DOI · Paper page
- 10.1016/j.xphs.2019.07.016 · DOI
- 10.1016/j.cep.2016.07.017 · DOI
- 10.1021/op300107z · DOI
- 10.1021/acs.oprd.6b00332 · DOI
- 10.1021/op5001918 · DOI
- 10.1016/j.cogsc.2018.03.005 · DOI
- 10.1021/acs.oprd.6b00359 · DOI
- 10.1039/C6CS00830E · DOI
- 10.3762/bjoc.13.97 · DOI
- 10.1002/anie.201004637 · DOI
- 10.1016/j.cep.2009.11.009 · DOI
- 10.1556/1846.2017.00023 · DOI
- 10.1039/C7RE00176B · DOI
- 10.1039/C7GC02421E · DOI
- 10.1002/cctc.201701619 · DOI
- 10.1039/C7CS00631D · DOI · Paper page
- 10.1021/acs.jchemed.7b00719 · DOI
- 10.1038/nprot.2017.102 · DOI
- 10.1021/ed3006083 · DOI
- 10.1021/acs.oprd.9b00178 · DOI
- 10.1016/j.jfluchem.2008.06.007 · DOI
- 10.1021/cr00012a002 · DOI
- 10.1139/v81-375 · DOI
- Baer H. P., 1966, Mol. Pharmacol., 2, 67
- 10.1038/nature25749 · DOI
- 10.1021/cr500366b · DOI · Paper page
- 10.1039/C7OB03059B · DOI
- 10.1039/C4QO00020J · DOI
- 10.1021/ar9001763 · DOI
- 10.1021/acs.orglett.8b00793 · DOI
- 10.1021/acs.oprd.8b00340 · DOI
- 10.1021/om50005a008 · DOI
- Matteson D. S., 1995, Stereodirected Synthesis with Organoboranes, 10.1007/978-3-642-79709-5 · DOI
- 10.1021/jo4013942 · DOI · Paper page
- 10.1021/om50003a004 · DOI
- 10.1002/anie.196405131 · DOI
- 10.1002/anie.196700411 · DOI · Paper page
- 10.1002/anie.197204731 · DOI
- 10.1021/acs.orglett.6b03753 · DOI
- 10.1021/acs.oprd.9b00336 · DOI
- 10.1002/jlac.19123940107 · DOI
- Kishner N. J., 1911, J. Russ. Chem. Soc., 43, 582
- cBurton, J. W. Comprehensive Organic Synthesis II ; Elsevier, Oxford, UK, 2014; Vol 8, pp 446–478. · DOI
- 10.1002/0471264180.or004.08 · DOI
- eWang, Z. Comprehensive Organic Name Reactions ; John Wiley & Sons, 2010; pp 3084–3089. · DOI · Paper page
- 10.1021/op400120g · DOI
- 10.1039/C5CS00902B · DOI · Paper page
- 10.1039/C7RE00021A · DOI
- 10.1021/op5002758 · DOI
- 10.1002/ceat.200500004 · DOI
- aPlouffe, P.; Macchi, A.; Roberge, D. In Flow Chemistry, Vol. 1: Fundamentals ; Darvas, F., Hessel, V., Dorman, G., Eds. De Gruyter: Berlin, 2014; p 139.
- bDencic, I.; Hessel, V. In Microreactors in Organic Synthesis and Catalysis , 2nd ed. Wirth, T., Ed. Wiley-VCH: Weinheim Germany, 2013; p 373. · DOI
- 10.1021/op200347k · DOI
- 10.1021/acs.oprd.9b00125 · DOI
- Anastas P. T., 1998, Green Chemistry: Theory and Practice
- 10.1039/B703488C · DOI
- 10.1021/acs.oprd.5b00222 · DOI · Paper page
- 10.1021/ar500359m · DOI · Paper page
- 10.1055/s-0030-1258379 · DOI
- 10.1016/j.tet.2012.06.015 · DOI
- 10.1021/ol800376f · DOI
- 10.1021/jo801033y · DOI
- 10.1039/b925499d · DOI
- 10.1039/c3cc42575d · DOI
- 10.1021/acs.oprd.9b00381 · DOI
- 10.1021/acs.oprd.8b00192 · DOI
- 10.1021/ol503625z · DOI
- 10.1021/acs.oprd.8b00387 · DOI
- 10.1039/C7SC04606E · DOI
- 10.1021/jm00235a023 · DOI
- 10.1002/prac.19853270419 · DOI
- 10.1093/jat/33.9.595 · DOI
- 10.1021/jo00339a010 · DOI
- 10.1021/acs.oprd.8b00213 · DOI
- 10.1039/C5RE00021A · DOI
- 10.1039/C7RE00024C · DOI
- 10.1021/acssuschemeng.7b02687 · DOI
- 10.3762/bjoc.8.229 · DOI · Paper page
- 10.1021/acs.oprd.9b00378 · DOI
- 10.1021/acscentsci.8b00728 · DOI
- 10.1556/1846.2017.00020 · DOI
- 10.1021/acs.accounts.9b00412 · DOI · Paper page
- 10.1021/acs.oprd.8b00379 · DOI
- 10.1039/C7CS00906B · DOI · Paper page
- 10.1021/acs.oprd.8b00305 · DOI · Paper page
- 10.1021/acs.oprd.9b00132 · DOI
Cited by
A field guide to flow chemistry for synthetic organic chemists
Capaldo, L., Wen, Z., & Noël, T. (2023) · Chemical Science · doi:10.1039/d3sc00992k · Cited by 402
PLGA-based nanomedicines manufacturing: Technologies overview and challenges in industrial scale-up
Operti, M. C., Bernhardt, A., Grimm, S., Engel, A., Figdor, C. G., & Tagit, O. (2021) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2021.120807 · Cited by 302
Dallinger, D., Gutmann, B., & Kappe, C. O. (2020) · Accounts of Chemical Research · doi:10.1021/acs.accounts.0c00199 · Cited by 163
Masui, H., & Fuse, S. (2022) · Organic Process Research & Development · doi:10.1021/acs.oprd.2c00074 · Cited by 38
Nakahara, Y., Endo, Y., Matsuda, Y., Nagaki, A., Takahashi, K., Kawaguchi, T., & Kato, K. (2024) · Synthesis · doi:10.1055/a-2077-6187 · Cited by 5
Metadata
- Authors
- Baumann, M., Moody, T. S., Smyth, M., & Wharry, S.
- Venue
- Organic Process Research & Development
- Publisher
- American Chemical Society (ACS)
- Published
- 2020-01-10
- Volume
- 24
- Issue
- 10
- Pages
- 1802-1813
- ISSN
- 1083-6160 (ISSN-L)
- 1520-586X
- OpenAlex
- W3000043886
- Cited by
- 487
- References
- 2
- FWCI
- 20.42
- Type
- journal article
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.