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Synthesis of macrolide antibiotics Communication 2. Synthesis of the C9-C13 fragment of erythronolides A and C and megalonolide
Authors:A. F. Sviridov  M. S. Ermolenko  N. K. Kochetkov
Affiliation:(1) N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow
Abstract:Conclusions The synthesis of the C9-C13 fragment of erythromycin A has been accomplished, starting from levoglusan (18 steps, 3.4%).For previous communications, see [1, 2].Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2561–2568, November, 1982.
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