David_MacMillan
David_MacMillan
David_MacMillan
MacMillan has also extensively developed photoredox catalysis for use in organic synthesis.[24][25][26]
Between 2010 and 2014, MacMillan was the founding editor-in-chief of the journal Chemical Science,
the flagship general chemistry journal published by the Royal Society of Chemistry.[16]
As of March 2024, MacMillan has an h-index of 125 according to Google Scholar[27] and of 115
according to Scopus.[28]
Visit to Brasil
In April 2024, David MacMillan was in Brazil for events at the State University of Rio de Janeiro and the
University of São Paulo.[29] In Rio, MacMillan asked to visit the headquarters of General Severiano, from
Botafogo, and was received by the Club's board of directors.[30] Later in São Paulo, MacMillan held a
short panel at University of São Paulo Chemistry Institute (IQ-USP) about his history as a researcher and
recent Nobel laureate. In September 2024, he will attend the Brazilian Meeting on Organic Synthesis in
Bento Gonçalves, Rio Grande do Sul, as opening lecture.
List
List of Nobel laureates affiliated with Princeton University
List of Nobel laureates
References
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17. MacMillan, David William Cross (1996). Stereocontrolled formation of bicyclic
tetrahydrofurans; and, Enantioselective total synthesis of eunicellin diterpenes (Ph.D.
thesis). University of California, Irvine. OCLC 35966904 (https://search.worldcat.org/oclc/35
966904). ProQuest 304225710 (https://www.proquest.com/docview/304225710).
18. Castelvecchi, Davide; Stoye, Emma (6 October 2021). " 'Elegant' catalysts that tell left from
right scoop chemistry Nobel" (https://doi.org/10.1038%2Fd41586-021-02704-2). Nature. 598
(7880). Springer Science and Business Media LLC: 247–248.
Bibcode:2021Natur.598..247C (https://ui.adsabs.harvard.edu/abs/2021Natur.598..247C).
doi:10.1038/d41586-021-02704-2 (https://doi.org/10.1038%2Fd41586-021-02704-2).
ISSN 0028-0836 (https://search.worldcat.org/issn/0028-0836). PMID 34616090 (https://pub
med.ncbi.nlm.nih.gov/34616090). S2CID 238422185 (https://api.semanticscholar.org/Corpu
sID:238422185).
19. Ahrendt, Kateri A.; Borths, Christopher J.; MacMillan, David W. C. (15 April 2000). "New
Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic
Diels−Alder Reaction". Journal of the American Chemical Society. 122 (17). American
Chemical Society (ACS): 4243–4244. doi:10.1021/ja000092s (https://doi.org/10.1021%2Fja
000092s). ISSN 0002-7863 (https://search.worldcat.org/issn/0002-7863).
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n.edu/faculty/david-macmillan). Princeton University Department of Chemistry. 21 July
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7 October 2021. Retrieved 7 October 2021.
21. Paras, Nick A.; MacMillan, David W. C. (12 June 2002). "The Enantioselective
Organocatalytic 1,4-Addition of Electron-Rich Benzenes to α,β-Unsaturated Aldehydes" (http
s://resolver.caltech.edu/CaltechAUTHORS:20170414-104130125). Journal of the American
Chemical Society. 124 (27). American Chemical Society (ACS): 7894–7895.
doi:10.1021/ja025981p (https://doi.org/10.1021%2Fja025981p). ISSN 0002-7863 (https://se
arch.worldcat.org/issn/0002-7863). PMID 12095321 (https://pubmed.ncbi.nlm.nih.gov/12095
321).
22. Jen, Wendy S.; Wiener, John J. M.; MacMillan, David W. C. (26 September 2000). "New
Strategies for Organic Catalysis: The First Enantioselective Organocatalytic 1,3-Dipolar
Cycloaddition" (https://resolver.caltech.edu/CaltechAUTHORS:20170406-070216339).
Journal of the American Chemical Society. 122 (40). American Chemical Society (ACS):
9874–9875. doi:10.1021/ja005517p (https://doi.org/10.1021%2Fja005517p). ISSN 0002-
7863 (https://search.worldcat.org/issn/0002-7863).
23. Paras, Nick A.; MacMillan, David W. C. (13 April 2001). "New Strategies in Organic
Catalysis: The First Enantioselective Organocatalytic Friedel−Crafts Alkylation" (https://resol
ver.caltech.edu/CaltechAUTHORS:20170411-120017472). Journal of the American
Chemical Society. 123 (18). American Chemical Society (ACS): 4370–4371.
doi:10.1021/ja015717g (https://doi.org/10.1021%2Fja015717g). ISSN 0002-7863 (https://se
arch.worldcat.org/issn/0002-7863). PMID 11457218 (https://pubmed.ncbi.nlm.nih.gov/11457
218).
24. Prier, Christopher K.; Rankic, Danica A.; MacMillan, David W. C. (19 March 2013). "Visible
Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic
Synthesis" (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4028850). Chemical Reviews.
113 (7): 5322–5363. doi:10.1021/cr300503r (https://doi.org/10.1021%2Fcr300503r).
ISSN 0009-2665 (https://search.worldcat.org/issn/0009-2665). PMC 4028850 (https://www.n
cbi.nlm.nih.gov/pmc/articles/PMC4028850). PMID 23509883 (https://pubmed.ncbi.nlm.nih.g
ov/23509883).
25. Shaw, Megan H.; Twilton, Jack; MacMillan, David W. C. (19 August 2016). "Photoredox
Catalysis in Organic Chemistry" (https://doi.org/10.1021/acs.joc.6b01449). The Journal of
Organic Chemistry. 81 (16): 6898–6926. doi:10.1021/acs.joc.6b01449 (https://doi.org/10.10
21%2Facs.joc.6b01449). ISSN 0022-3263 (https://search.worldcat.org/issn/0022-3263).
PMC 4994065 (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4994065). PMID 27477076
(https://pubmed.ncbi.nlm.nih.gov/27477076).
26. Nicewicz, David A.; MacMillan, David W. C. (3 October 2008). "Merging Photoredox
Catalysis with Organocatalysis: The Direct Asymmetric Alkylation of Aldehydes" (https://ww
w.ncbi.nlm.nih.gov/pmc/articles/PMC2723798). Science. 322 (5898): 77–80.
Bibcode:2008Sci...322...77N (https://ui.adsabs.harvard.edu/abs/2008Sci...322...77N).
doi:10.1126/science.1161976 (https://doi.org/10.1126%2Fscience.1161976). PMC 2723798
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2723798). PMID 18772399 (https://pubmed.
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39. "Past Recipients of the Harrison Howe Award" (https://www.sas.rochester.edu/chm/howe/pa
st.html). Retrieved 7 October 2021.
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External links
David MacMillan (https://www.nobelprize.org/laureate/1003) on Nobelprize.org