1997 - Izaak Walton Killam Memorial Prize, Canada Council
1996 - Prix Marie-Victorin, Government of Quebec
1988 - Fellow of the Royal Society of Canada Academy of Science
1988 - Chemical Institute of Canada Medal
Stephen Hanessian spends much of his time researching Stereochemistry, Organic chemistry, Total synthesis, Bicyclic molecule and Combinatorial chemistry. His Stereochemistry research incorporates elements of Amino acid, Enzyme, Peptidomimetic, Chemical synthesis and Stereoselectivity. His Stereoselectivity study integrates concerns from other disciplines, such as Medicinal chemistry and Addition reaction.
His Organic chemistry study is mostly concerned with Lactone, Reagent, Catalysis, Alkyl and Acetal. His work focuses on many connections between Total synthesis and other disciplines, such as Absolute configuration, that overlap with his field of interest in Natural product. Stephen Hanessian focuses mostly in the field of Bicyclic molecule, narrowing it down to topics relating to Alkylation and, in certain cases, Enantiomer, Enantioselective synthesis and Reactivity.
Stereochemistry, Organic chemistry, Total synthesis, Combinatorial chemistry and Bicyclic molecule are his primary areas of study. He is interested in Intramolecular force, which is a field of Stereochemistry. His study in Organic chemistry concentrates on Alkyl, Catalysis, Reagent and Lactone.
His work deals with themes such as Lactam and Crystal structure, which intersect with Bicyclic molecule. Crystal structure is closely attributed to Molecule in his study.
Stephen Hanessian mostly deals with Stereochemistry, Total synthesis, Organic chemistry, Combinatorial chemistry and Catalysis. Stephen Hanessian mostly deals with Lactone in his studies of Stereochemistry. His research in Total synthesis intersects with topics in Molecule, Aliskiren, Enantiopure drug and Pactamycin.
All of his Organic chemistry and Yield and Allylic rearrangement investigations are sub-components of the entire Organic chemistry study. His studies in Combinatorial chemistry integrate themes in fields like Reagent and In vitro. Stephen Hanessian focuses mostly in the field of Catalysis, narrowing it down to matters related to Medicinal chemistry and, in some cases, Alkyl.
His scientific interests lie mostly in Stereochemistry, Total synthesis, Organic chemistry, Aminoglycoside and Antibiotics. His Stereochemistry research is multidisciplinary, relying on both Antiprotozoal, Stereoisomerism, Antibacterial activity, Pactamycin and Chemical synthesis. His study in Total synthesis is interdisciplinary in nature, drawing from both Stereocenter, Lactone, Lewis acids and bases, Enantiopure drug and Stereoselectivity.
The Stereoselectivity study which covers Reagent that intersects with Combinatorial chemistry. His Organic chemistry research is multidisciplinary, incorporating elements of Perspective and Drug. The concepts of his Aminoglycoside study are interwoven with issues in Ether, A-site, Amphiphile and Neomycin.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Design and synthesis of conformationally constrained amino acids as versatile scaffolds and peptide mimetics
Stephen Hanessian;Grant McNaughton-Smith;Henry-Georges Lombart;William D. Lubell.
Regioselective manipulation of hydroxyl groups via organotin derivatives
S. David;S. Hanessian.
The Preparation and Synthetic Utility of tert-Butyldiphenylsilyl Ethers
Stephen Hanessian;Pierre Lavallee.
Canadian Journal of Chemistry (1975)
Analysis of trimethylsilyl derivatives of carbohydrates by gas chromatography and mass spectrometry
Don C. DeJongh;T. Radford;Jeremy D. Hribar;Stephen Hanessian.
Journal of the American Chemical Society (1969)
trans-1,2-Diaminocyclohexane Derivatives as Chiral Reagents, Scaffolds, and Ligands for Catalysis: Applications in Asymmetric Synthesis and Molecular Recognition.
Youssef L. Bennani† and;Stephen Hanessian.
Chemical Reviews (1997)
Chemistry of the glycosidic linkage. An efficient synthesis of 1,2-trans-di-saccharides
Stephen Hanessian;Joseph Banoub.
Carbohydrate Research (1977)
Design of Secondary Structures in Unnatural Peptides: Stable Helical γ-Tetra-, Hexa-, and Octapeptides and Consequences of α-Substitution
Stephen Hanessian;Xuehong Luo;and Robert Schaum;Stephen Michnick.
Journal of the American Chemical Society (1998)
Synthesis of naturally occurring C-nucleosides, their analogs, and functionalized C-glycosyl precursors.
Stephen Hanessian;André G. Pernet.
Advances in Carbohydrate Chemistry and Biochemistry (1976)
Reaction of O-benzylidene sugars with N-bromosuccinimide. II. Scope and synthetic utility in the methyl 4,6-0-benzylidenehexopyranoside series
Stephen Hanessian;Nike R. Plessas.
Journal of Organic Chemistry (1969)
Synthesis of (4S)-hydroxymethyl-(2R)-(2-propyl)-butyrolactone: A quest for a practical route to an important hydroxyethylene isostere chiron
Stephen Hanessian;Teresa Abad-Grillo;Grant McNaughton-Smith.
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: