Prof. R B Sunoj

Areas Of Expertise

• 3-oxidopyrylium ylides
• Ab initio calculations
• AB-INITIO
• Acid-derivatives
• Acids
• Dctivated olefins
• Activation strain model
• Acyclic stereoselection
• Additions
• Adiabatic connection
• Agostic interactions
• Alcohols
• Aldehydes
• Aldol reaction
• Aldol reactions
• Alpha
• Alpha-alkylation
• Amination
• Asymmetric aldol reactions
• Asymmetric catalysis
• Asymmetric hydrovinylation
• Asymmetric Organic Reactions
• Asymmetric organocatalysis
• Atom transfer
• Atoms-in-Molecule
• Aziridination
• AZO-Compounds
• Azobispyridine
• Barrier heights
• basis-set,beta-unsaturated aldehydes
• Binuclear complexes
• Bis(hydrazine)
• Bridging ligands
• Building-blocks
• C-C coupling
• Carbenes
• Carbocyclic 8-membered rings
• Carbon-dioxide fixation
• Carbonyl addition
• Carbonyl-complexes
• Catalyzed cycloadditions
• Center-Dot-N
• Chiral auxiliaries
• Chiral diferrocenyl diselenides
• Chromophores
• Complexes
• Coordination chemistry
• Coupled electron-transfer
• Crystal-structures
• Cyclooctanoids
• Cyclotrimerizations
• Density
• Density functional calculations
• Density-functional theory
• Design
• DFT
• DFT calculations
• DFT studies
• Diastereofacial selectivities
• Diastereoselectivity
• Difluoride-diorganyl diselenides
• Dinuclear copper(ii) complexes
• Direct generation
• Effective core potentials
• Electrochemistry
• Electron transfer
• Electron-deficient alkenes
• Electrophilic selenium reagents
• Electrospray-ionization mass
• Enantioselective organocatalysis
• Enantioselective synthesis
• Epr
• EPR spectroscopy
• Exogenous bridges
• Explicit solvents
• Facial selectivity
• Functionalized NHC
• Gaussian-type basis
• Generalized gradient approximation
• H-2 activation
• Heck reaction
• Heterolytic dihydrogen activation
• Hiliman reaction
• Homogeneous hydrogenation
• Intramolecular aldol condensation
• Ketones
• Kinetics
• Lewis pair
• Lewis-acids
• Magnetic-properties
• Main-group
• Mannich
• Methyl vinyl ketone
• Michael addition
• Mixed-valent complexes
• Molecular-orbital methods
• Molecular-structure
• Molecules
• Morita-Baylis-Hillman Reaction.
• N
• N ligands
• N-sulfonated imnes
• Nanostructures
• Naphthalene peri positions
• Negative hyperconjugation
• Nickel(ii) complexes
• Nitrogen
• Nitrogen-heterocycles
• NMR chemical-shifts
• Nonbonding interaction
• O ligands
• Olefin metathesis
• Olefin polymerization
• Organic-synthesis
• Organocatalysis
• Organometallic catalysis
• Organoselenium compounds
• Origins
• Oxidation
• Oxyselenenylation-deselenenylation reactions
• Peptide-based catalysts
• Peroxidase-like activity
• Phosphine lewis-bases
• Phosphine-ligands
• Phosphorus
• Polarizable continuum model
• Polycycles
• Polymer
• Polymerization catalysts
• Proton transport
• Proton-transfer
• Quinonoid ligands
• Radical cations
• Radical complexes
• Radical ions
• Ray crystal-stucture
• Reaction mechanisms
• Reduction
• Relay proton transfer
• Rhodium complexes
• Ring contraction-rearrangement
• Ring-closing metathesis
• Ring-opening polymerization (ROP)
• Ruthenium
• Samarium(ii) iodide
• Schiff-base complexes
• Selenoenzyme glutathione-peroxidase
• Semi-empirical calculations
• Set model chemistry
• Silanetriols
• Silver
• Solvation free-energies
• Solvent effects
• Spectroelectrochemistry
• Stereoselectivity,Sulfur Ylide
• Taxane skeleton
• Thermochemical cycle
• Thermochemical kinetics
• Titanium enolate
• Titanium(iv) chloride
• Tosylated imines
• Transfers
• Transition states
• Transition states
• Valence-state distributions
• Water
• Water chemistry
• X-ray
• X-ray-stucture
• Ylides
• [5+3] cycloadditions
• AI/ML based approaches