Luke Schembri
Researcher at Department of Medicinal Chemistry; Drug Design and Discovery
- E-mail:
- luke.schembri@ilk.uu.se
- Visiting address:
- Biomedicinskt Centrum BMC, Husargatan 3
- Postal address:
- Box 574
751 23 UPPSALA
Short presentation
A researcher with experience in medicinal and organic chemistry research as well as chemistry education research at a university level. My current research focuses on the synthesis of novel matrices for MALDI mass spectrometry in order to detect various small molecule analytes with high sensitivity and selectivity.
Keywords
- palladium
- organic chemistry
- medicinal chemistry
- chemistry education
- carbonylation
Biography
Luke Schembri was born in Melton, Australia in 1990. He completed his Bachelor of Pharmaceutical Sciences (with Honours) at Monash University Parkville in 2011. He then completed his PhD under the supervision of Associate Professor Bim Graham and Professor Peter Scammells at the same institute which focused on the synthesis and biological evalution of fluorescent opiate ligands from 2012 to 2016. He then spent one year as a postdoctoral researcher on projects such as: the design and synthesis of fragment libraries as HIV reverse transcriptase inhibitors, the synthesis of covalently bound inhibitors for studies on the human muscarinic receptors and synthesis of Aminopeptidase N inhibitors for the treatment of cancer. He then moved to Uppsala University in Sweden in 2017 to continue post-doctoral studies under Associate Professor Luke Odell investigating the synthesis of acylsulfonamides as bioisosteres of carboxylic acids via palladium-catalysted carbonylative coupling.
Throughout his education, Luke has always kept a keen interest in chemistry education. Beginning from his undergraduate years, he has been involved in hosting extra tutorials for students seeking extra help in organic chemistry, has been a teaching associate in organic and physical chemistry during his PhD and now lectures and caretakes masters students at Uppsala University during their Fördjupningsprojekt i organisk farmaceutisk kemi course which they undertake in our laboratory. Additionally, he has worked closely with Dr Elizabeth Yuriev in chemistry education research, investigating student study habits and metacognition (problem solving).
Research
Luke's current research focuses on the synthesis and evaluation of novel, selective and sensitive matrices and reagents to be used in MALDI mass spectrometry.

Publications
Selection of publications
Palladium(0)-Catalyzed Carbonylative One-Pot Synthesis of N-Acylguanidines
Part of Journal of Organic Chemistry, p. 12520-12529, 2017
Recent publications
Part of Chemical Communications, p. 9238-9241, 2024
A Base-Free, Low Temperature Click and Release Reaction for the In Situ Generation of Diazomethane
Part of Advanced Synthesis and Catalysis, p. 1839-1845, 2023
- DOI for A Base-Free, Low Temperature Click and Release Reaction for the In Situ Generation of Diazomethane
- Download full text (pdf) of A Base-Free, Low Temperature Click and Release Reaction for the In Situ Generation of Diazomethane
Part of Journal of the American Society for Mass Spectrometry, p. 836-846, 2023
- DOI for On-Tissue Chemical Derivatization for Comprehensive Mapping of Brain Carboxyl and Aldehyde Metabolites by MALDI-MS Imaging
- Download full text (pdf) of On-Tissue Chemical Derivatization for Comprehensive Mapping of Brain Carboxyl and Aldehyde Metabolites by MALDI-MS Imaging
Part of ACS Chemical Biology, p. 147-158, 2022
- DOI for Region-Specific and Age-Dependent Multitarget Effects of Acetylcholinesterase Inhibitor Tacrine on Comprehensive Neurotransmitter Systems
- Download full text (pdf) of Region-Specific and Age-Dependent Multitarget Effects of Acetylcholinesterase Inhibitor Tacrine on Comprehensive Neurotransmitter Systems
Part of Science Advances, 2021
- DOI for Mass spectrometry imaging identifies abnormally elevated brain L-DOPA levels and extrastriatal monoaminergic dysregulation in L-DOPA-induced dyskinesia
- Download full text (pdf) of Mass spectrometry imaging identifies abnormally elevated brain L-DOPA levels and extrastriatal monoaminergic dysregulation in L-DOPA-induced dyskinesia
All publications
Articles in journal
Part of Chemical Communications, p. 9238-9241, 2024
A Base-Free, Low Temperature Click and Release Reaction for the In Situ Generation of Diazomethane
Part of Advanced Synthesis and Catalysis, p. 1839-1845, 2023
- DOI for A Base-Free, Low Temperature Click and Release Reaction for the In Situ Generation of Diazomethane
- Download full text (pdf) of A Base-Free, Low Temperature Click and Release Reaction for the In Situ Generation of Diazomethane
Part of Journal of the American Society for Mass Spectrometry, p. 836-846, 2023
- DOI for On-Tissue Chemical Derivatization for Comprehensive Mapping of Brain Carboxyl and Aldehyde Metabolites by MALDI-MS Imaging
- Download full text (pdf) of On-Tissue Chemical Derivatization for Comprehensive Mapping of Brain Carboxyl and Aldehyde Metabolites by MALDI-MS Imaging
Part of ACS Chemical Biology, p. 147-158, 2022
- DOI for Region-Specific and Age-Dependent Multitarget Effects of Acetylcholinesterase Inhibitor Tacrine on Comprehensive Neurotransmitter Systems
- Download full text (pdf) of Region-Specific and Age-Dependent Multitarget Effects of Acetylcholinesterase Inhibitor Tacrine on Comprehensive Neurotransmitter Systems
Part of Science Advances, 2021
- DOI for Mass spectrometry imaging identifies abnormally elevated brain L-DOPA levels and extrastriatal monoaminergic dysregulation in L-DOPA-induced dyskinesia
- Download full text (pdf) of Mass spectrometry imaging identifies abnormally elevated brain L-DOPA levels and extrastriatal monoaminergic dysregulation in L-DOPA-induced dyskinesia
Part of Journal of Chemical Education, p. 3217-3222, 2020
Palladium(0)-Catalyzed Carbonylative Synthesis of N-Acylsulfonamides via Regioselective Acylation
Part of Journal of Organic Chemistry, p. 6970-6981, 2019
Carbonylations beyond aryl-X: Development of new multicomponent reactions
Part of Abstracts of Papers of the American Chemical Society, 2018
Palladium(0)-Catalyzed Carbonylative One-Pot Synthesis of N-Acylguanidines
Part of Journal of Organic Chemistry, p. 12520-12529, 2017