Biography:David MacMillan
Sir David MacMillan | |
---|---|
Born | David William Cross MacMillan 16 March 1968 Bellshill, Scotland, United Kingdom |
Citizenship | United Kingdom United States[1] |
Education | Bellshill Academy |
Alma mater | University of Glasgow (BSc) University of California, Irvine (MSc, PhD) |
Awards | Corday-Morgan medal Member of the National Academy of Sciences (2018) Nobel Prize in Chemistry (2021) |
Scientific career | |
Institutions | |
Thesis | Stereocontrolled formation of bicyclic tetrahydrofurans and Enantioselective total synthesis of eunicellin diterpenes (1996) |
Doctoral advisor | Larry E. Overman |
Other academic advisors | Ernest W. Colvin David A. Evans |
Doctoral students | Vy Dong, Tehshik Yoon |
Website | Official website |
Sir David William Cross MacMillan FRS FRSE (born 16 March 1968)[2] is a Scottish[8] chemist and the James S. McDonnell Distinguished University Professor of Chemistry at Princeton University, where he was also the chair of the Department of Chemistry from 2010 to 2015.[9][10] He shared the 2021 Nobel Prize in Chemistry with Benjamin List "for the development of asymmetric organocatalysis".[11] MacMillan used his share of the $1.14 million prize to establish the May and Billy MacMillan Foundation.[12]
Education and early life
MacMillan was born in Bellshill, North Lanarkshire, Scotland, in 1968 and grew up in nearby New Stevenston.[13] He attended the local state-funded schools, New Stevenston Primary and Bellshill Academy, and credited his Scottish education and Scottish upbringing for his success.[14][13]
He received his undergraduate degree in chemistry at the University of Glasgow, where he worked with Ernie Colvin.[15][16]
In 1990, he left the UK to begin his doctoral studies under the direction of Professor Larry Overman at the University of California, Irvine. During this time, he focused on the development of new reaction methodology directed toward the stereocontrolled formation of bicyclic tetrahydrofurans. MacMillan's graduate studies culminated in the total synthesis of 7-(−)-deacetoxyalcyonin acetate, a eunicellin diterpenoid isolated from the soft coral Eunicella stricta.[17] He earned his Ph.D. in 1996.[16]
Career and research
Upon receiving his PhD., MacMillan accepted a position with Professor David Evans at Harvard University. His postdoctoral studies centered on enantioselective catalysis, in particular, the design and development of Sn(II)-derived bisoxazoline complexes (Sn(II)box).[16]
MacMillan began his independent research career as a member of the chemistry faculty at the University of California, Berkeley in July 1998. He joined the department of chemistry at Caltech in June 2000, where his group's research interests centered on new approaches to enantioselective catalysis. In 2004, he was appointed as the Earle C. Anthony Professor of Chemistry. He became the James S. McDonnell Distinguished University Professor at Princeton University in September 2006.[16]
He is considered to be one of the founders of organocatalysis.[18] In 2000, MacMillan designed small organic molecules that can provide or accept electrons and therefore efficiently catalyse reactions.[18][19] He developed catalysts that can drive asymmetric catalysis, in which a reaction produces more of the left-handed version of a molecule than the right-handed one (chirality), or vice versa.[18] MacMillan's research group has made many advances in the field of asymmetric organocatalysis, and they have applied these new methods to the synthesis of a range of complex natural products.[16][18] He developed chiral imidazolidinone catalysts.[20][19][21] MacMillan catalysts (de) are used in various asymmetric syntheses. Examples include Diels-Alder reactions,[19] 1,3-dipolar cycloadditions,[22] Friedel-Crafts alkylations[23] or Michael additions.[21]
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 2021), MacMillan has an h-index of 110 according to Google Scholar[27] and of 100 according to Scopus.[28]
Honours and awards
MacMillan was knighted in the 2022 Birthday Honours for services to chemistry and science.[29][30]
- 2002 – Sloan Research Fellowship[31]
- 2004 – Corday-Morgan medal of Royal Institute of Chemistry[32]
- 2012 – Elected a Fellow of the Royal Society (FRS)[33][34]
- 2012 – Elected as a member of the American Academy of Arts and Sciences[35]
- 2013 – Elected a Corresponding Fellow of the Royal Society of Edinburgh (FRSE)[36]
- 2015 – Harrison Howe Award[37]
- 2017 – Ryoji Noyori Prize[38]
- 2018 – Elected a member of the National Academy of Sciences[16]
- 2021 – Nobel Prize in Chemistry[11]
List
- List of Nobel laureates affiliated with Princeton University
- List of Nobel laureates
References
- ↑ 1.0 1.1 "Princeton's David MacMillan receives Nobel Prize in chemistry". 6 October 2021. https://www.princeton.edu/news/2021/10/06/princetons-david-macmillan-receives-nobel-prize-chemistry.
- ↑ "David W.C. MacMillan". Nobel Foundation. https://www.nobelprize.org/prizes/chemistry/2021/macmillan/facts/.
- ↑ "David MacMillan: 'Being Scottish helped me win Nobel Prize'". BBC News. 7 October 2021. https://www.bbc.com/news/uk-scotland-58828279. Retrieved 15 October 2021.
- ↑ Paterson, Laura (2021-10-06). "Scottish scientist jointly wins Nobel Prize in chemistry" (in en). https://www.standard.co.uk/news/uk/nobel-prize-scottish-german-princeton-university-chemistry-b959099.html.
- ↑ "Chemistry Nobel awarded for mirror-image molecules" (in en-GB). BBC News. 2021-10-06. https://www.bbc.com/news/science-environment-58814418.
- ↑ Russell, Jennifer (2021-10-06). "Scots scientist wins Nobel Prize for chemistry" (in en). https://www.dailyrecord.co.uk/scotland-now/scots-scientist-wins-nobel-prize-25151568.
- ↑ "Scottish scientist jointly wins Nobel Prize in chemistry" (in en-GB). https://uk.news.yahoo.com/scottish-scientist-jointly-wins-nobel-120108141.html.
- ↑ [1][3][4][5][6][7]
- ↑ "The MacMillan Group" (in en-US). http://chemlabs.princeton.edu/macmillan/.
- ↑ "David MacMillan". 15 December 2016. https://www.organicdivision.org/eminentorganicchemists/david-macmillan/.
- ↑ 11.0 11.1 "The Nobel Prize in Chemistry 2021" (in en-US). https://www.nobelprize.org/prizes/chemistry/2021/summary/.
- ↑ Service, Purdue News. "David MacMillan, the 2021 Nobel laureate in chemistry, to join President Chiang for Presidential Lecture Series on Feb. 13" (in en). https://www.purdue.edu/newsroom/releases/2023/Q1/david-macmillan,-the-2021-nobel-laureate-in-chemistry,-to-join-president-chiang-for-presidential-lecture-series-on-feb.-13.html.
- ↑ 13.0 13.1 "David MacMillan: 'Being Scottish helped me win Nobel Prize'" (in en-GB). BBC News. 7 October 2021. https://www.bbc.com/news/uk-scotland-58828279.
- ↑ "Success wouldn't have happened if I wasn't Scottish, says Bellshill-born Nobel Prize winner" (in en). https://www.heraldscotland.com/business_hq/19631329.professor-david-wc-macmillan-success-wouldnt-happened-wasnt-scottish/.
- ↑ "Bellshill man and former Glasgow University student David WC MacMillan wins the Nobel prize for chemistry". Glasgow Times. https://www.glasgowtimes.co.uk/news/19630090.bellshill-man-former-glasgow-university-student-david-wc-macmillan-wins-nobel-prize-chemistry/.
- ↑ 16.0 16.1 16.2 16.3 16.4 16.5 16.6 "David MacMillan". National Academy of Sciences. http://www.nasonline.org/member-directory/members/20044093.html.
- ↑ 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. ProQuest 304225710.
- ↑ 18.0 18.1 18.2 18.3 Castelvecchi, Davide; Stoye, Emma (6 October 2021). "'Elegant' catalysts that tell left from right scoop chemistry Nobel". Nature (Springer Science and Business Media LLC) 598 (7880): 247–248. doi:10.1038/d41586-021-02704-2. ISSN 0028-0836. PMID 34616090. Bibcode: 2021Natur.598..247C.
- ↑ 19.0 19.1 19.2 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 (American Chemical Society (ACS)) 122 (17): 4243–4244. doi:10.1021/ja000092s. ISSN 0002-7863.
- ↑ "David MacMillan". 21 July 2014. https://chemistry.princeton.edu/faculty/david-macmillan.
- ↑ 21.0 21.1 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". Journal of the American Chemical Society (American Chemical Society (ACS)) 124 (27): 7894–7895. doi:10.1021/ja025981p. ISSN 0002-7863. PMID 12095321.
- ↑ 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". Journal of the American Chemical Society (American Chemical Society (ACS)) 122 (40): 9874–9875. doi:10.1021/ja005517p. ISSN 0002-7863. https://resolver.caltech.edu/CaltechAUTHORS:20170406-070216339.
- ↑ Paras, Nick A.; MacMillan, David W. C. (13 April 2001). "New Strategies in Organic Catalysis: The First Enantioselective Organocatalytic Friedel−Crafts Alkylation". Journal of the American Chemical Society (American Chemical Society (ACS)) 123 (18): 4370–4371. doi:10.1021/ja015717g. ISSN 0002-7863. PMID 11457218.
- ↑ Prier, Christopher K.; Rankic, Danica A.; MacMillan, David W. C. (2013-03-19). "Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis". Chemical Reviews 113 (7): 5322–5363. doi:10.1021/cr300503r. ISSN 0009-2665. PMID 23509883.
- ↑ Shaw, Megan H.; Twilton, Jack; MacMillan, David W. C. (2016-08-19). "Photoredox Catalysis in Organic Chemistry". The Journal of Organic Chemistry 81 (16): 6898–6926. doi:10.1021/acs.joc.6b01449. ISSN 0022-3263. PMID 27477076. PMC 4994065. https://doi.org/10.1021/acs.joc.6b01449.
- ↑ Nicewicz, David A.; MacMillan, David W. C. (2008-10-03). "Merging Photoredox Catalysis with Organocatalysis: The Direct Asymmetric Alkylation of Aldehydes". Science 322 (5898): 77–80. doi:10.1126/science.1161976. PMID 18772399. Bibcode: 2008Sci...322...77N.
- ↑ {{Google Scholar id}} template missing ID and not present in Wikidata.
- ↑ David MacMillan publications indexed by the Scopus bibliographic database. (Subscription content?)
- ↑ No. 63714. 1 June 2022. p. B2. https://www.thegazette.co.uk/London/issue/63714/supplement/B2
- ↑ Newsroom, The (8 June 2022). "Nobel prize winning chemist from Bellshill has now been knighted by the Queen". https://www.glasgowworld.com/education/nobel-prize-winner-david-macmillan-from-bellshill-has-been-knighted-by-the-queen-3724790.
- ↑ "MacMillan Awarded Sloan Research Fellowship". California Institute of Technology. August 2002. https://www.caltech.edu/about/news/macmillan-awarded-sloan-research-fellowship-594. Retrieved 6 October 2021.
- ↑ "Caltech Faculty Awards and Honors 2004–2005". California Institute of Technology. Archived from the original on 11 August 2011. https://web.archive.org/web/20110811133849/http://annual-report.caltech.edu/documents/21-ar_04_05_awards.pdf. Retrieved 20 June 2012.
- ↑ "New Fellows 2012". Royal Society. http://royalsociety.org/about-us/fellowship/new-fellows-2012/. Retrieved 20 June 2012.
- ↑ "Sir David MacMillan's Royal Society Fellowship Biography" (in en). https://royalsociety.org/people/david-macmillan-11867/.
- ↑ "David W.C. MacMillan" (in en). https://www.amacad.org/person/david-wc-macmillan.
- ↑ "Professor David William Cross MacMillan FRS, CorrFRSE – The Royal Society of Edinburgh" (in en-GB). The Royal Society of Edinburgh. https://www.rse.org.uk/fellow/david-macmillan/.
- ↑ "Past Recipients of the Harrison Howe Award". https://www.sas.rochester.edu/chm/howe/past.html.
- ↑ "The Society of SynthRyoji Noyori Prize Recipients" (in ja). Society of Synthetic Organic Chemistry, Japan. https://www.ssocj.jp/english/NoyoriPrize/recipients.html. Retrieved 2 November 2017.
External links
- Miss nobel-id as parameter
Original source: https://en.wikipedia.org/wiki/David MacMillan.
Read more |