CHROMATOGRAPHIC RESOLUTION. 7. USEFUL CHIRAL PACKING MATERIALS FOR HIGH‐PERFORMANCE LIQUID CHROMATOGRAPHIC RESOLUTION OF ENANTIOMERS: PHENYLCARBAMATES OF POLYSACCHARIDES COATED ON SILICA GEL
Synthesis of Fluorinated Cycloalkyl N‐Phenylcarbamates and Their Microbial Defluorination/Oxygenation by Beauveria bassiana
Method of Assay for Isopropyl N-Phenylcarbamate
Optical resolution of dihydropyridine enantiomers by high-performance liquid chromatography using phenylcarbamates of polysaccharides as a chiral stationary phase
Synthesis of 2‐Acetamido‐2‐deoxy‐D‐gluconhydroximolactone‐ and Chitobionhydroximolactone‐Derived N‐Phenylcarbamates, Potential Inhibitors of β‐N‐Acetylglucosaminidase
Enantioseparation by Using Chitin Phenylcarbamates as Chiral Stationary Phases for High-Performance Liquid Chromatography
Alkylation of allylic derivatives. 4. On the mechanism of alkylation of allylic N-phenylcarbamates with lithium dialkylcuprates
Enantioseparation on 4‐halogen‐substituted phenylcarbamates of amylose as chiral stationary phases for high‐performance liquid chromatography
The nature of the transition state in ester pyrolysis. Part II. The relative rates of pyrolysis of ethyl, isopropyl, and t-butyl acetates, phenylacetates, benzoates, phenyl carbonates, and N-phenylcarbamates
Alkaline hydrolysis of substituted phenyl N-phenylcarbamates. Structure–reactivity relationships consistent with an E1cB mechanism
