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Tetracyclines
Authors:M. N. Kolosov  A. I. Gurevich  Yu. B. Shvetsov
Affiliation:(1) Institute for the Chemistry of Natural Products, Academy of Sciences, USSR
Abstract:Summary As a result of a spectropolarimetric comparison of the phthalidecarboxylic products (IIIa) and (IIIb)of the degradation of aureomycin with specially synthesized 3S-(-)-3-methyl-3-phthalidecarboxylic acid (IV), the absolute configuration (I) was proved for tetracycline and 7-halotetracyclines and was postulated for 5-hydroxy- and 6-de-methyl- tetracyclines.For Communications 13–15 see [1-3].
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