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{{Arabic name|'''العسري'''|العسري}} {{Family name hatnote|lang=Arabic|'''العسري'''|العسري}}
{{Infobox scientist {{Infobox scientist
| name = Jamal Lasri | name = Jamal Lasri

Revision as of 15:26, 18 December 2024

Moroccan-Portuguese Chemist
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In this Arabic name, the surname is العسري.
Jamal Lasri
Born1973
Casablanca
Nationality Morocco
Citizenship Portugal
Alma materUniversity of Valencia
University of Hassan II Casablanca
Scientific career
FieldsOrganic Chemistry, Coordination Chemistry and Catalysis
InstitutionsKing Abdulaziz University, Jeddah

Instituto Superior Técnico, University of Lisbon

Jaume I University
Doctoral advisorProf. José Sepúlveda-Arques http://www.uv.es/sepulved/

Jamal Lasri (in Arabic: جمال العسري) was born in 1973 in Casablanca, is a Portuguese-Moroccan synthetic Chemist. He received his B.Sc. degree in Chemistry from the University of Hassan II Casablanca (Morocco) in 1997. Then, he moved to Spain for his M.Sc. and Ph.D. studies at the Faculty of Pharmacy of the University of Valencia under the supervision of Prof. José Sepúlveda-Arques. His work was focused on the synthesis of pyridopyrimidine-2,4-diones, novel route for the synthesis of N-tosylguanidines by ring cleavage of 1,2-dihydro-2-tosyliminopyrimidines and study of the intermolecular transamidation reactions of N-carbamoylmethyl-N’-tosylguanidines with primary amines. He obtained his M.Sc. and Ph.D. degrees in organic chemistry in 2002 and 2004, respectively (Excellent "Cum Laude").

Crystal structure of one of the molecules of (1,3,5,7,9-pentaazanona-1,3,6,8-tetraenato) platinum(II) complex reported by Jamal Lasri and coworkers in Inorg. Chem. 2012, 51, 10774.
Partial stick representation of the crystal packing diagram of bis-(pyrrolidin-2-ylidene)-phthalamide palladium(II) complex reported by Jamal Lasri and coworkers in Chem. -Eur. J. 2008, 14, 9312.

Career

In September 2004, he started his postdoctoral research funded by a fellowship from Fundación Bancaja - Caja Castellón at the Jaume I University of Castellón (Spain) joining the group of Prof. Santiago Vicente Luis Lafuente. He worked on the design and synthesis of new copper bis(oxazoline) polymeric systems and their use as heterogeneous catalysts for cyclopropanation reactions.

In May 2005, he moved to Portugal to work as a postdoctoral researcher with a Fundação para a Ciência e Tecnologia fellowship in the group of Prof. Armando J. L. Pombeiro at the Instituto Superior Técnico of the University of Lisbon.

In January 2008, he was appointed associate researcher (Science 2007 program) at the Instituto Superior Técnico. His research interests involved the activation of organonitriles by transition metal centers, metal-mediated synthesis of N-heterocyclic compounds via cycloaddition, thermal and microwave-assisted transition metal-catalyzed cross-coupling reactions for carbon-carbon bond construction (e.g. Suzuki-Miyaura, Mizoroki–Heck types) in water, peroxidative oxidation of alcohols, alkanes and green chemistry.

In September 2013, he holds a position of associate professor of organic chemistry at King Abdulaziz University (Saudi Arabia). Since June 2015, he is Full Professor of organic chemistry.

Lasri discovered that azines are also produced when chalcone reacts with a hydrazone to furnish 3,5-diphenyl-1H-pyrazole.. In addition, together with Armando J. L. Pombeiro and João J. R. Fraústo da Silva they reported the first example of oxadiazoline and ketoimine palladium(II) complexes as highly efficient catalytic systems for Suzuki reaction in supercritical carbon dioxide (scCO2).

References

  1. http://www.uv.es/sepulved/
  2. R. Mamouni, M. Aadil, M. Akssira, J. Lasri, J. Sepúlveda. Tetrahedron Lett. 2003, 44, 2745. http://dx.doi.org/10.1016/S0040-4039(03)00273-9
  3. J. Lasri, M. E. González, J. Sepúlveda. Synthesis 2003, 845. http://dx.doi.org/10.1055/s-2003-38684
  4. P. Fernandez, A. Ubeda, I. Guillén, J. Lasri, M. E. González, M. Akssira, J. Sepúlveda. Eur. J. Med. Chem. 2003, 38, 289. http://dx.doi.org/10.1016/S0223-5234(03)00013-8
  5. M. E. González, E. Castillo, J. Lasri, J. Sepúlveda. Prog. React. Kinet. Mech. 2004, 29, 311.
  6. J. Lasri, M. E. González, J. Sepúlveda. Org. Lett. 2003, 5, 3851. http://dx.doi.org/10.1021/ol035377z
  7. https://dialnet.unirioja.es/servlet/tesis?codigo=217687
  8. http://www.uji.es/CA/departaments/qio/estructura/personal/e@/22752?p_per_id=65302
  9. J. Lasri, M. N. Kopylovich, M. F. C. Guedes da Silva, M. A. Januário Charmier, A. J. L. Pombeiro, Chem. -Eur. J. 2008, 14, 9312. http://dx.doi.org/10.1002/chem.200800510
  10. J. Lasri, M. A. Januário Charmier, M. Haukka, A. J. L. Pombeiro, J. Org. Chem. 2007, 72, 750. http://dx.doi.org/10.1021/jo061659b
  11. J. Lasri, M. F. C. Guedes da Silva, M. N. Kopylovich, S. Mukhopadhyay, M. A. Januário Charmier, A. J. L. Pombeiro, Dalton Trans. 2009, 2210. http://dx.doi.org/10.1039/b813996b
  12. J. Lasri, T. C. O. Mac Leod, A. J. L. Pombeiro, Appl. Catal. A: Gen. 2011, 397, 94. http://dx.doi.org/10.1016/j.apcata.2011.02.019
  13. P. J. Figiel, M. N. Kopylovich, J. Lasri, M. F. C. Guedes da Silva, J. J. R. Fraústo da Silva, A. J. L. Pombeiro, Chem Commun. 2010, 46, 2766. http://dx.doi.org/10.1039/b922738e
  14. M. N. Kopylovich, Y. Yu. Karabach, M. F. C. Guedes da Silva, P. J. Figiel, J. Lasri, A. J. L. Pombeiro, Chem. -Eur. J. 2012, 18, 899. http://dx.doi.org/10.1002/chem.201101688
  15. R. R. Fernandes, J. Lasri, M. F. C. Guedes da Silva, J. A. L. da Silva, J. J. R. Fraústo da Silva, A. J. L. Pombeiro, Appl. Catal. A: Gen. 2011, 402, 110. http://dx.doi.org/10.1016/j.apcata.2011.05.035
  16. R. R. Fernandes, J. Lasri, A. M. Kirillov, M. F. C. Guedes da Silva, J. A. L. da Silva, J. J. R. Fraústo da Silva, A. J. L. Pombeiro, Eur. J. Inorg. Chem. 2011, 3781. http://dx.doi.org/10.1002/ejic.201100460
  17. J. Lasri, A. I. Ismail, Indian J. Chem. Sect. B. 2018, 57B, 362. http://nopr.niscpr.res.in/handle/123456789/43824
  18. R. R. Fernandes, J. Lasri, M. F. C. Guedes da Silva, A. M. F. Palavra, J. A. L. da Silva, J. J. R. Fraústo da Silva, A. J. L. Pombeiro, Adv. Synth. Catal. 2011, 353, 1153. http://dx.doi.org/10.1002/adsc.201000909

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