References
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- Kraus , G. A. and Sugimoto , H. ibid. , 1978 2263 van Leusen, A. M. and Terpstra, J. W., ibid., 1981, 5097
- Iwai , K. , Kosugi , H. , Uda , H. and Kawai , M. 1977 . Bull. Chem. Soc. Jpn. , 50 : 242 The lactones(1a-d) were prepared effectively by the procedure reported The compounds (1e and 1f) were prepared in high yield by the oxidation of the corresponding α-phenylthiolactones which were obtained from the reaction of the naked lactones and diphenyl disulfide in the presence of LDA.
- Reichert , B. and Koch , W. 1935 . Arch. Pharm. , 273 : 265 Its methylation afforded 2-(2, 4-dimethoxyphenyl)- ethanol as colorless crystals, mp 66–67°. (mp 67°
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- Suginome , H. and Iwadare , T. 1966 . Bull. Chem. Soc. Jpn. , 39 : 1535 This compound was obtained by reduction of a isoflavone derivative as the synthetic intermediate of d,1-homopterocarpin