Dr. Krishna Swamy. G

synthesis reactions procedure nmr types aromaticity electrophilic aromatic substitution reaction acetanilide experiment preparation cycloaddition reaction configuration reformatsky reaction regioselectivity chiral auxiliary asymmetric synthesis sawhorse newmann stereochemistry formic acid condensation reaction benzimidazole coumarins resorcinol pechmann condensation solvent free oxone bromo napthol 2-naphthol lattice energy spinels magnetic properties color aom pi bonding sigma bonding mot lft cft hydroformylation reaction cobalt complex wacker oxidation palladium complex carbonylation reaction zirconium comple coordination numbers stereoisomerism iupac nomenclature ligands coordination compounds simmon smith reaction organozinc reagent gilman reagent organocuprates grignard reagent organomagnesium compounds organolithium reagents nomenclature of drugs pharmacophore therapeutic index ic50 ld50 medicine drug threo-erythro d-l convention cip rule chiral center fischer dash-wedge vit b12 fadh2 nad biotin vit k lipoic acid coa plp tpp coenzymes biochemical mechanism p-nitroacetanilide hydrolysis p-bromoaniline p-bromoacetanilide phosphoramidite approach phosphotriester phosphodiester onucleotide synthesis olig rna dna nucleotide nucleoside nucleic acid hunsdiecker reaction peroxides nbs meerwein arylation gomberg-bachmann reaction kolbes electrolysis benzylic halogenation allylic halogenation free radicals diastereoselectivity reetz model prelogs rule crams rule chiral ligands binalh asymmetric aldol reaction asymmetric induction enantiomeric excess coordination complexes binary mixture functional group analysis organic chemistry semi micro qualitative analysis pass analysis docking studies admet 123-triazole ethyl ester of p-aminobenzoic acid p-aminobenzoic acid p-nitrobenzoic acid phenylhydrazine acetophenone phenylindole format mass ir factors affecting chemical shift chemical shift reagents second order first order karplus curve coupling constant instrumentation principle chemical shift 1h answers questions covid-19 benzene-sulfide benzene-oxide valence tautomers seven membered heterocycles theipine oxepine chemoselectivity organomanganese reagents sextet theory hydrazines dipolar cycloaddition reaction sydnones mesoionic heterocycles octant rule alpha axial haloketone sector rule lactam 3h-azepine 1h-azepine 4h-azepine azacycloheptatriene electron deficient dienes inverse electron demand diels-alder reaction isomers tetrazine heterocycle julia olefination sulfur ylides thioethers thiols cyanuric chloride cyanuric acid inverse demand diels-alder reaction heterocycles 135-triazine 124-triazine 123-triazine anti and syn eliminations peterson olefination ipso substitution organosilanes reducing agent mitsunobu reaction wittig reaction nomenclature phosphites phosphines organophosphorus anomalous x-ray scattering cotton effect ord cd optical rotation relative absolute pyrazine diazine six membered heterocyclic compound pyrimidine diazines protonolysis cyanidation isomerization carbonylation synthesis of aldehyde oxidation to alcohols hydroboration reaction organoboranes aromatic character pyridine heterocyle crystal field splitting tetrahedral octahedral cfse fukuyama coupling negishi coupling barbier reaction cyclopropanation simmon-smith reaction organozinc chemoselective reagent cecl3 nabh4 luche reduction retro dipolar cycloaddition dipolar cycloaddition alkynes allenes oxidizing agent alkene ozone ozonolysis unconjugated diene set birch reduction asymmetric dihydroxylation asymmetric epoxidation stereospecific stereoselective receptor theories drug administration receptors enzymes adme structure free ware molecule chemsketch diastereotopic ligands & faces homotopic enantiotopic prochirality d-l & erythro-threo m-p convention r-s nomenclature flying wedge representation solvent free grind stone technique