References
- H. Ohta and H. Tetsukawa, Chem. Lett., 1979, 1379.
- J.W. Cornforth and R.H. Cornforth “Natural Substances Formed Biologically from Mevalonic Acid,” ed. by T.W.Goodwin, Academic Press, New York, N.Y., 1970, p. 5.
- G. Tamura, K. Ando, K. Kodama and K. Arima, Appl. Microbiol., 16, 965 (1968).
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- Mevalonolactone; PMR \delta _{TMS}^{CDC{I_3}}$ d jms'3: 1-37 (s, 3H), 1.89 (m, 2H), 2.55 (m, 2H), 3.37 (broad s, 1H), 4.2~4.8 (m, 2H). IR \nu _{mzx}^{KBr}$:3400, 2960, 2910, 1720, 1235, 1125, 1065, 1020, 930, 880, 800. Benzhydryl amide mp. 96~97°C. Anal. Found: C, 70.24; H, 7.14; N, 4.24. Calcd for C17H23NO3: C, 70.56; H, 8.01; N, 4.84%.
- F.C. Haug, L.F.H. Lee, R.S.D. Mittal, P.R. Ravikuman, J.A. Chan, C.J. Sih, E. Capsi and C.R. Eck, J. Am. Chem. Soc., 97, 4144 (1975).
- A.J. Irwin and J.B. Jones, J. Am. Chem. Soc., 99, 556 (1977).