References
- Muller , C. J. , Kepner , R. E. and Webb , A. D. 1973 . Amer. J. Enol. Viticult. , 24 : 5
- Kuwamura , T. and Takahashi , H. 1969 . Bull. Chem. Soc. Jap. , 42 : 1345
- Fairbourne , A. , Gibson , G. P. and Stephens , D. W. 1932 . J. Chem. Soc. , : 1965
- Webb , A. D. , Eriksson , K. , Muller , C. J. and Kepner , R. E. 1976 . Amer. J. Enol. Viticult. , 27 : 27
- Stevens , M. A. E. I. duPont de Nemours and Company . U.S. Patent #2, 859, 218 . 1958 .
- Schenck , G. O. 1953 . Liebigs Ann. Chem. , 584 : 156
- This was found to be especially true of the products resulting from ethanol
- An exception to this was the 5-(2-phenylethoxy)-2(5H)-furanone which required 24 hours under the same reaction conditions to undergo reduction
- Spinning band distillation was necessary to get a pure sample of the 5-ethoxydihydro-2(3H)-furanone
- Kovats , E. 1965 . Advan. Chromatog. , 1 : 229 Retention indices were calculated as recommended by Kovats
- The 5-(2-phenylethoxy)dihydro-2(3H)-furanone did not give a sufficiently well-formed peak under any chromatographic conditions tried to permit calculation of meaningful retention indices