2-Anthrylmethoxyacetic acid, a new chiral anisotropic reagent for elucidating the absolute configuration of acyclic alcohols

This publication has 6 references indexed in Scilit:

• Conformational Structure and Dynamics of Arylmethoxyacetates: DNMR Spectroscopy and Aromatic Shielding Effect
  The Journal of Organic Chemistry, 1995
• New chiral anisotropic reagents, NMR tools to elucidate the absolute configurations of long-chain organic compounds
  Tetrahedron Letters, 1994
• Determination of the Absolute Configuration of Ginnol, a Long-chain Aliphatic Alcohol, by Use of a New Chiral Anisotropic Reagent
  Chemistry Letters, 1994
• On the use of the O-methylmandelate ester for establishment of absolute configuration of secondary alcohols
  The Journal of Organic Chemistry, 1986
• Syntheses of selected .epsilon.-(2- or 9-anthryl)alkanoic acids and certain esters - carbon-13 spin-lattice relaxation time measurements of methyl 5-(2-anthryl)pentanoate and methyl 7-(2-anthryl)heptanoate
  The Journal of Organic Chemistry, 1981
• Synthesis of .alpha.-methoxyaliphatic acids from chloroform and aliphatic aldehydes with sodium hydride as catalyst in tetrahydrofuran
  The Journal of Organic Chemistry, 1978