A5060250150- Lubricants and Their Additives
- Enzyme Catalysis and Immobilization
- Inorganic and Organometallic Chemistry
- Synthetic Organic Chemistry Methods
- Bacterial Identification and Susceptibility Testing
- Tribology and Wear Analysis
- Microbial Metabolic Engineering and Bioproduction
- Asymmetric Synthesis and Catalysis
- Chemical Synthesis and Reactions
- Lipid metabolism and biosynthesis
- Marine Toxins and Detection Methods
- Polymer Nanocomposites and Properties
- Image Processing and 3D Reconstruction
- Organic Chemistry Cycloaddition Reactions
- Photopolymerization techniques and applications
- Synthesis and characterization of novel inorganic/organometallic compounds
- Coordination Chemistry and Organometallics
- Tribology and Lubrication Engineering
- Antibiotics Pharmacokinetics and Efficacy
- Global Energy and Sustainability Research
- Leaf Properties and Growth Measurement
- Axial and Atropisomeric Chirality Synthesis
- Fatty Acid Research and Health
- Spectroscopy and Chemometric Analyses
- Synthesis and Biological Activity
De La Rue (United Kingdom)
2020-2024
Wantage Community Hospital
2023
Springer Nature (Germany)
2009
Castrol (United Kingdom)
1992-1994
Tun Abdul Razak Research Centre
1986-1990
Royal Holloway University of London
1979-1982
Abstract Developing a geometric formulation of any biological object has number justifications and applications. Recently, we developed universal figure for describing bird's egg in the possible basic shapes: spherical, ellipsoidal, ovoid, pyriform. The proved widely applicable but had drawbacks, including very obvious join between two parts egg. To correct this, Main Axiom mathematical formula. This essentially involved making ordinate extremum function correspond to half maximum breadth (...
α-Hydroxyalkylcyclopropanes are oxidised by nicotinamide-dependent horse liver alcohol dehydrogenase without cleavage of the 3-membered ring, implying that radical intermediates improbable in these reactions.
The oxidation of exo-bicyclo[4.1.0]heptan-7-ylmethanol and bicyclo[4.1.0]heptan-2-ol the reduction corresponding carbonyl compounds by horse liver alcohol dehydrogenase (E.C.1.1.1.1) occur without cleavage three-membered ring. Reactions these substrates with hydride donating abstracting reagents also proceed retention small ring whereas radical reactions lead to cyclopropane These results, together kinetic studies on rates opening cyclopropylmethyl silyl ethers e.s.r. spectroscopy suggest...
This article describes a method of curve-fitting that involves splitting the curve into two (or more) and creating separate functions for each part. These are then concatenated via linking function to create one overall better original data than is otherwise achievable. The able do this by separating so they active in only relevant portion without use dummy variables. final result continuous which it straightforward smooth transition at knot between piecewise subfunctions. In addition,...
A series of monocyclic and bicyclic cyclopropylmethanols typified by bicyclo[4.1.0]heptan-7-ylmethanol is shown to comprise latent irreversible inhibitors horse liver alcohol dehydrogenase (E.C.1.1.1.1) with inhibitory properties related the ability inhibitor bind enzyme. The time course inhibition biphasic, a property shared number unsaturated aldehydes, ketones, alcohols. Kinetic studies also suggest that occurs most effectively during removal hydride from as oxidation takes place....
Abstract Formaldehyde undergoes ethylaluminum dichloride‐catalyzed ene reaction with jojoba oil to afford a mixture of 1∶1 and 1∶2 adducts. The hydroxymethyl products were identified by comparison model adducts prepared from methyl oleate oleyl acetate.
Reduction of cyclopropaneglyoxylic acid by lactate dehydrogenase and model systems for both alcohol dehydrogenases occurs without cleavage the three-membered ring implying that radical intermediates are improbable in these reactions.