David L. Hughes mainly focuses on Medicinal chemistry, Stereochemistry, Crystal structure, Ligand and Crystallography. His Medicinal chemistry research is multidisciplinary, relying on both Imine, Adduct, Organic chemistry, Alkyl and Deprotonation. The various areas that David L. Hughes examines in his Stereochemistry study include Chemical synthesis, Nucleophile, Cycloaddition and Amide.
David L. Hughes combines subjects such as Yield, Tetrahydrofuran, Inorganic chemistry, Chelation and Substituent with his study of Crystal structure. His work deals with themes such as Allylic rearrangement, Catalysis, Norbornadiene and Single crystal, which intersect with Ligand. His Crystallography study combines topics in areas such as Hydrazone, Molecule and Metal.
His scientific interests lie mostly in Crystal structure, Crystallography, Stereochemistry, Medicinal chemistry and Molecule. His Crystal structure research includes themes of Inorganic chemistry, Molybdenum, Ligand and Hydrogen bond. He studies Denticity which is a part of Ligand.
His Crystallography research incorporates themes from Ion, Protonation, Electrochemistry and Metal. The concepts of his Stereochemistry study are interwoven with issues in Octahedron, Tetrahydrofuran, Vanadium and Ring. His Medicinal chemistry research also works with subjects such as
David L. Hughes spends much of his time researching Crystallography, Crystal structure, Stereochemistry, Medicinal chemistry and Ligand. His Crystallography research incorporates elements of Relaxation, Atom, Electron paramagnetic resonance, Hydrogen bond and Electrochemistry. His Crystal structure course of study focuses on Atom and Sulfite and Bioinformatics.
David L. Hughes has researched Stereochemistry in several fields, including Dihedral angle, Bond length, Cyclopentadienyl complex, Amide and Methyl group. The various areas that David L. Hughes examines in his Medicinal chemistry study include Benzene, Polymerization, Solvent, Ring and Catalysis. His Ligand research includes elements of Pyridine and Molecule.
David L. Hughes focuses on Stereochemistry, Photochemistry, Medicinal chemistry, Catalysis and Organic chemistry. David L. Hughes merges many fields, such as Stereochemistry and Solid-state, in his writings. His work carried out in the field of Medicinal chemistry brings together such families of science as Aryl, Brønsted–Lowry acid–base theory and Ligand.
He has included themes like Peroxide and Alkyl in his Catalysis study. His research investigates the connection between Organic chemistry and topics such as Electrochemistry that intersect with problems in Borohydride, Hydrogen fuel, Metal ions in aqueous solution and Crystal structure. Crystallography is closely connected to Chromophore in his research, which is encompassed under the umbrella topic of Triphenylene.
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Are heterogeneous catalysts precursors to homogeneous catalysts
Ian W. Davies;Louis Matty;David L. Hughes;Paul J. Reider.
Journal of the American Chemical Society (2001)
Mechanistic Studies of the Suzuki Cross-Coupling Reaction
George B. Smith;George C. Dezeny;David L. Hughes;Anthony O. King.
Journal of Organic Chemistry (1994)
A mechanistic study of the Mitsunobu esterification reaction
D. L. Hughes;R. A. Reamer;J. J. Bergan;E. J. J. Grabowski.
Journal of the American Chemical Society (1988)
Titanium, zinc and alkaline-earth metal complexes supported by bulky O,N,N,O-multidentate ligands: syntheses, characterisation and activity in cyclic ester polymerisation.
Yann Sarazin;Ruth H. Howard;David L. Hughes;Simon M. Humphrey.
Dalton Transactions (2006)
A di-iron dithiolate possessing structural elements of the carbonyl/cyanide sub-site of the H-centre of Fe-only hydrogenase
Alban Le Cloirec;Sian C. Davies;David J. Evans;David L. Hughes.
Chemical Communications (1999)
Ligand transfer reactions of mixed-metal lanthanide/magnesium allyl complexes with β-diketimines: Synthesis, structures, and ring-opening polymerization catalysis
Luis F. Sánchez-Barba;David L. Hughes;Simon M. Humphrey;Manfred Bochmann.
Organometallics (2006)
A thermally stable gold(III) hydride: synthesis, reactivity, and reductive condensation as a route to gold(II) complexes.
Dragoş-Adrian Roşca;Dan A. Smith;David L. Hughes;Manfred Bochmann.
Angewandte Chemie (2012)
Gold peroxide complexes and the conversion of hydroperoxides into gold hydrides by successive oxygen-transfer reactions
Dragoş-Adrian Roşca;Joseph A Wright;David L Hughes;Manfred Bochmann.
Nature Communications (2013)
Aryl Trihydroxyborates: Easily Isolated Discrete Species Convenient for Direct Application in Coupling Reactions
Andrew N. Cammidge;Victoria H. M. Goddard;Hermant Gopee;Nicola L. Harrison.
Organic Letters (2006)
Acidities of carboxamides, hydroxamic acids, carbohydrazides, benzenesulfonamides, and benzenesulfonohydrazides in DMSO solution
F. G. Bordwell;Herbert E. Fried;David L. Hughes;Tsuei Yun Lynch.
Journal of Organic Chemistry (1990)
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