Schmidt Rearrangement

Acid-catalyzed reaction of carbonyls with HN?, forming amides or amines.

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Synthesis Oxidation IR spectroscopy Asymmetric synthesis Enantiomer Regioisomer Regioselectivity Lewis acid Yield NMR spectroscopy Catalyst Strecker synthesis Equilibrium Mass spectrometry Selectivity Hydrogenation Nucleophile Electrophile Heck reaction Solvent reflux Stereochemistry Reduction Enantioselectivity Steric hindrance Enantiomeric excess (ee) Deprotonation Rearrangement Chromatography Recrystallization Hydrolysis Esterification Baylis-Hillman reaction Nucleophilic substitution Cross-coupling Mitsunobu reaction Dipolarophile Kinetics Conformation Radical Diastereoselective Michael reaction Conjugate addition Bischler-Napieralski reaction Ullmann reaction TLC (thin-layer chromatography) NMR (nuclear magnetic resonance) Proton transfer Dehydrogenation Protecting group

Chemical Baike