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Oluwarotimi Stephen Ojo
Also known as: O. Stephen Ojo
University of Glasgow, University of Liverpool, Newcastle University, University of East Anglia
Research areas: Chemistry · Inorganic Chemistry · Crystal structures of chemical compounds · Crystallography and molecular interactions · Crystal Structures and Properties
0000-0002-3514-3744
About
Exploration of metal-hydride in asymmetric catalysis and natural product synthesis
Employment
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University of Glasgow Lecturer in Organic Chemistry2022 - 2024
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University of Liverpool Research Associate in Medicinal Chemistry2021 - 2022
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University of East Anglia Senior Research Associate2019 - 2021
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University of Cambridge Research Associate2016 - 2018
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University of St Andrews Research Fellow2014 - 2016
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GlaxoSmithKline Research and Development Research/Placement Student2007 - 2008
Education
- 2009 - 2014
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Newcastle University MChem2005 - 2009
Projects & Funding
Projects & funding information is unavailable.
Publications (13)
- Synthesis of a chiral dinuclear Cu(ii)-benzothiazolamine complex: evidence of cuprophilic interaction in its structure and exploration of its electrochemical properties and catalytic performance Save
- Double asymmetric synthesis: faster reactions are more selective and a model to estimate relative rate Save
- An expedient copper-catalysed asymmetric synthesis of γ-lactones and γ-lactams. Application to the synthesis of lucidulactone A Save
- Expeditious access to cis-β-aryl, γ-alkyl disubstituted (±)-γ-butyrolactones via nickel-hydride catalysis Save
- Bacterial Catabolism of β-Hydroxypropiovanillone and β-Hydroxypropiosyringone Produced in the Reductive Cleavage of Arylglycerol-β-Aryl Ether in Lignin Save
- Synthesis of the natural product descurainolide and cyclic peptides from lignin-derived aromatics Save
- Isothiourea-Catalysed Acylative Kinetic Resolution of Aryl-Alkenyl (sp2vs. sp2) Substituted Secondary Alcohols Save
- The synthesis and analysis of lignin-bound Hibbert ketone structures in technical lignins Save
- Total synthesis of dehaloperophoramidine using a highly diastereoselective Hosomi–Sakurai reaction Save
- Isolation of Functionalized Phenolic Monomers through Selective Oxidation and CO Bond Cleavage of the β‐O‐4 Linkages in Lignin Save
- A convenient, economical and scalable multi-gram synthesis of 1-vinylcyclopropyl 4-methylbenzenesulfonate Save
- Diaryl- and triaryl-pyrrole derivatives: inhibitors of the MDM2–p53 and MDMX–p53 protein–protein interactions Save
- Efficient Multigram Syntheses of Air-Stable, Chiral Primary Phosphine Ligand Precursors via Palladium-Catalyzed Phosphonylation of Aryltriflates Save