1993 - Meldola Medal and Prize, Royal Society of Chemistry (UK)
His scientific interests lie mostly in Catalysis, Transfer hydrogenation, Organic chemistry, Ruthenium and Noyori asymmetric hydrogenation. His work in Catalysis covers topics such as Formic acid which are related to areas like Hydrogen and Triethylamine. His Transfer hydrogenation research incorporates themes from Combinatorial chemistry, Polymer chemistry and Imine.
He studies Organic chemistry, focusing on Borane in particular. Martin Wills combines subjects such as Asymmetric hydrogenation, Dimer and Base with his study of Ruthenium. His work carried out in the field of Noyori asymmetric hydrogenation brings together such families of science as Ketone, Enantiomer, Medicinal chemistry and Photochemistry.
His primary scientific interests are in Catalysis, Organic chemistry, Transfer hydrogenation, Enantioselective synthesis and Medicinal chemistry. The concepts of his Catalysis study are interwoven with issues in Combinatorial chemistry, Ketone, Polymer chemistry and Formic acid. Martin Wills has included themes like Hydrogen and Triethylamine in his Formic acid study.
His research on Transfer hydrogenation concerns the broader Ruthenium. His studies in Enantioselective synthesis integrate themes in fields like Intramolecular force, Allylic rearrangement and Hydrosilylation. His study focuses on the intersection of Medicinal chemistry and fields such as Stereochemistry with connections in the field of Stereoselectivity.
Martin Wills mostly deals with Catalysis, Transfer hydrogenation, Combinatorial chemistry, Medicinal chemistry and Organic chemistry. While the research belongs to areas of Catalysis, he spends his time largely on the problem of Amine gas treating, intersecting his research to questions surrounding Diamine. His Transfer hydrogenation study is associated with Ruthenium.
His Combinatorial chemistry study incorporates themes from Yield, Reagent, Denticity, Enantioselective synthesis and Substrate. The various areas that Martin Wills examines in his Medicinal chemistry study include Alkyne, Acetophenone, Steric effects and Biphenyl. Martin Wills works in the field of Organic chemistry, namely Alcohol.
His primary areas of investigation include Catalysis, Transfer hydrogenation, Organic chemistry, Combinatorial chemistry and Polymer chemistry. His studies in Transfer hydrogenation integrate themes in fields like Aryl, Asymmetric hydrogenation, Sodium formate and Medicinal chemistry. The various areas that Martin Wills examines in his Asymmetric hydrogenation study include Noyori asymmetric hydrogenation, Ruthenium and Phosphine.
The Medicinal chemistry study combines topics in areas such as Enantiomeric excess, Alkyne, Ring and Steric effects. His Cyclopentadienone and Amine gas treating investigations are all subjects of Organic chemistry research. Martin Wills has researched Combinatorial chemistry in several fields, including Hydrogen and Enantioselective synthesis.
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Asymmetric transfer hydrogenation of C=O and C=N bonds
Matthew J. Palmer;Martin Wills.
Tetrahedron-asymmetry (1999)
Hydrogen generation from formic acid and alcohols using homogeneous catalysts
Tarn C. Johnson;David J. Morris;Martin Wills.
Chemical Society Reviews (2010)
A new class of "tethered" ruthenium(II) catalyst for asymmetric transfer hydrogenation reactions.
Jérôme Hannedouche;Guy J Clarkson;Martin Wills.
Journal of the American Chemical Society (2004)
A class of ruthenium(II) catalyst for asymmetric transfer hydrogenations of ketones.
Aidan M Hayes;David J Morris;Guy J Clarkson;Martin Wills.
Journal of the American Chemical Society (2005)
Enantioselective catalysis using phosphorus-donor ligands containing two or three P-N or P-O bonds.
Jeffrey Ansell;Martin Wills.
Chemical Society Reviews (2002)
Chemistry and clinical biology of the bryostatins.
Roger Mutter;Martin Wills.
Bioorganic & Medicinal Chemistry (2000)
The "reverse-tethered" ruthenium (II) catalyst for asymmetric transfer hydrogenation: further applications.
David J. Morris;and Aidan M. Hayes;Martin Wills.
Journal of Organic Chemistry (2006)
C-N bond formation between alcohols and amines using an iron cyclopentadienone catalyst.
Andrew J. Rawlings;Louis J. Diorazio;Martin Wills.
Organic Letters (2015)
Asymmetric catalysis using iron complexes – ‘Ruthenium Lite’?
Muftah Darwish;Martin Wills.
Catalysis Science & Technology (2012)
(1R,2S)-(+)-cis-1-Amino-2-indanol: An Effective Ligand for Asymmetric Catalysis of Transfer Hydrogenations of Ketones
Matthew Palmer;Tim Walsgrove;Martin Wills.
Journal of Organic Chemistry (1997)
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