Conclusions
A stereodirected synthesis of erythronolide B carbon chain was carried out starting from from levoglucosan.
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A. F. Sviridov, V. S. Borodkin, M. S. Ermolenko, and D. V. Yashunskii, Izv. Akad. Nauk SSSR, Ser. Khim., No. 3, 680 (1989).
A. F. Sviridov, G. E. Berdimbetova, and N. K. Kochetkov, Izv. Akad. Nauk SSSR, Ser. Khim., 2572 (1982).
S. Masamune, H. Hirama, S. Mori, et al., J. Am. Chem. Soc.,103, 1568 (1981).
D. A. Evans and K. T. Chapman, Tetrahedron Lett.,27, 5939 (1986).
Y. Oikawa, T. Nishi, and O. Yonemitsu, Tetrahedron Lett.,24, 4037 (1983).
A. F. Sviridov, M. S. Ermolenko, D. V. Yashunskii, et al., Izv. Akad. Nauk SSSR, Ser. Khim., No. 2, 438 (1989).
Y. Oikawa, T. Tanaka, and O. Yonemitsu, Tetrahedron Lett.,27, 3647 (1986).
A. F. Sviridov, M. S. Ermolenko, D. V. Yashunskii, et al., Izv. Akad. Nauk SSSR, Ser. Khim., No. 2, 447 (1989).
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For previous communication, see [1].
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 688–693, March, 1989.
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Sviridov, A.F., Borodkin, V.S., Ermolenko, M.S. et al. Synthesis of macrolide antibiotics. 18. Stereospecific building up of the carbon chain of erythronolide B. Russ Chem Bull 38, 614–619 (1989). https://doi.org/10.1007/BF00958059
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DOI: https://doi.org/10.1007/BF00958059