Jordi Burés

Jordi Burés is a Senior Lecturer in the Department of Chemistry at The University of Manchester.[5] His research in general is on the areas of organic and physical chemistry, specizalizing in Mechanistic Studies,nuclear magnetic resonance and catalysis.[6][7]

Jordi Burés
Jordi Burés
Born
Jordi Burés
Alma materUniversity of Barcelona(Bsc., MRes., PhD)[1]
Known forMechanistic Studies
catalysis
Nuclear Magnetic Resonance
AwardsRoyal Society of Chemistry Hickinbottom Award (2020) [2]
Young Researcher Award from the Spanish Royal Society of Chemistry (2019) [3]
Thieme Chemistry Journals Award (2018) [4]
Scientific career
FieldsOrganic Chemistry
Physical Chemistry
InstitutionsImperial College London[1]
University of Manchester[5]
ThesisAplicació i estudis mecànics de les reaccions de trimetilfosfina i diversos activadors amb nitrocompostos alifàtics, oximes i azides (2009)
Doctoral advisorJaume Vilarrasa

Education

Burés completed his Bachelor of Science at University of Barcelona in 2003.[1] He then continued to pursue his MRes and his Doctor of Philosophy degrees in the same university with Jaume Vilarrasa and successfully completed it in 2009.[5]

Research and career

After graduating, Burés was awarded a postdoctoral fellowship with Prof. Donna Blackmond at The Scripps Research Institute in California.[8] He later joined the Chemistry Department at Imperial College London in 2013 as a Imperial College Junior Research Fellow and moved to University of Manchester in 2016 as a lecturer in organic chemistry.[1][9]

His research in general is on the areas of organic and physical chemistry, specizalizing in Mechanistic Studies,nuclear magnetic resonance and catalysis.[6][7]

Notable work

In 2016, Burés produced a new simple graphical method to elucidate the order in catalyst, where a normalized time scale t[cat]Tn was shown to be able to adjust entire reaction profiles constructed with concentration data.[10] The research further showed that compared to methods that used rates, the proposed method is faster, simple, requires fewer experiments and minimizes effects of experimental errors.[11] This method is generally known as Variable Time Normalization Analysis.[12] [13]

In 2012, Burés, Blackmond and Armstrong led a mechanistic study on conjugate addition of aldehydes to nitro-olefins and the α-chlorination of aldehydes catalyzed by diarylprolinol ether which was able to show that the stereochemical outcome of products of both of these reactions is not determined by the transition state of the step in which the stereogenic center is formed but rather is correlated with the relative stability and reactivity of diastereomeric intermediates downstream in the catalytic cycle. This hence provided evidence to suggest that this concept may represent a general phenomenon for pyrrolidine-based catalysts lacking an acidic directing proton.[14][15]

Awards and nominations

Major Publications
  • Bures, Jordi; Companyó, Xavier (2017). "Distribution of Catalytic Species as an Indicator To Overcome Reproducibility Problems". Journal of American Chemical Society. 139 (25): 8432–8435. doi:10.1021/jacs.7b05045. Retrieved 31 January 2021.
  • Bures, Jordi (2016). "A Simple Graphical Method to Determine the Order in Catalyst". Angewandte Chemie International Edition. 55 (6): 2028–2031. doi:10.1002/anie.201508983. Retrieved 31 January 2021.
  • Bures, Jordi (2016). "Variable time normalization analysis: General graphical elucidation of reaction orders from concentration profiles". Angewandte Chemie International Edition. 128 (52): 16318–16321. doi:10.1002/ange.201609757. Retrieved 31 January 2021.
  • Bures, Jordi; Armstrong, Alan; Blackmond, Donna G (2012). "Curtin–Hammett paradigm for stereocontrol in organocatalysis by diarylprolinol ether catalysts". Journal of American Chemical Society. 134 (15): 6741–6750. doi:10.1021/ja300415t. Retrieved 31 January 2021.
  • Bures, Jordi; Armstrong, Alan; Blackmond, Donna G (2011). "Mechanistic Rationalization of Organocatalyzed Conjugate Addition of Linear Aldehydes to Nitro-olefins". Journal of American Chemical Society. 133 (23): 8822–8825. doi:10.1021/ja203660r. Retrieved 31 January 2021.

References
  1. Imperial College London. "Dr. Jordi Bures (Visiting Researcher)". Retrieved 31 January 2021.
  2. Royal Society of Chemistry. "2020 Royal Society of Chemistry Award Winners". Retrieved 31 January 2021.
  3. Spanish Royal Society of Chemistry. "Concesión de los Premios RSEQ 2019". Retrieved 31 January 2021.
  4. Thieme Chemistry. "Thieme Chemistry Journals Award". Retrieved 31 January 2021.
  5. University of Manchester. "Dr. Jordi Bures". Retrieved 31 January 2021.
  6. University of Manchester. "Dr. Jordi Bures Research". Retrieved 31 January 2021.
  7. "Dr. Jordi Bures (Google Scholar)". Retrieved 31 January 2021.
  8. Scripps Research. "Blackmond Lab Personnel". Retrieved 31 January 2021.
  9. "Jordi Bures (About)". Retrieved 31 January 2021.
  10. Bures, Jordi (2016). "A Simple Graphical Method to Determine the Order in Catalyst". Angewandte Chemie International Edition. 55 (6): 2028–2031. doi:10.1002/anie.201508983. Retrieved 31 January 2021.
  11. Sabatini, Marco T.; Boulton, Lee T.; Sheppard, Tom D. (2017). "Borate esters: Simple catalysts for the sustainable synthesis of complex amides". Science Advances. 3 (9). doi:10.1126/sciadv.1701028. Retrieved 31 January 2021.
  12. Bures, Jordi; T. Nielsen, Christian D. (2019). "Visual kinetic analysis". Chemical Science. 10 (2): 348–353. doi:10.1039/C8SC04698K. Retrieved 31 January 2021.
  13. Jordi Bures (YouTube). "Visual Kinetic Analysis". Retrieved 31 January 2021.
  14. Bures, Jordi; Armstrong, Alan; Blackmond, Donna G (2012). "Curtin–Hammett paradigm for stereocontrol in organocatalysis by diarylprolinol ether catalysts". Journal of American Chemical Society. 134 (15): 6741–6750. doi:10.1021/ja300415t. Retrieved 31 January 2021.
  15. Bures, Jordi; Armstrong, Alan; Blackmond, Donna G (2012). "Kinetic correlation between aldehyde/enamine stereoisomers in reactions between aldehydes with α-stereocenters and chiral pyrrolidine-based catalysts". Chemical Science. 3 (4): 1273–1277. doi:10.1039/C2SC01082H. Retrieved 31 January 2021.
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