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Synthesis of heterocyclic systems with carbohydrate fragment
Authors:A. V. Samet  Y. P. Kislyi  N. B. Chernyshova  D. N. Reznikov  B. I. Ugrak  V. V. Semenov
Affiliation:(1) Russian Academy of Sciences, N. D. Zelinsky Institute of Organic Chemistry, 47 Leninsky prosp., 117913 Moscow, Russia
Abstract:The reactions of levoglucosenone with amides of several agr-nitrocarboxylic acids and acetoacetic acid result in tetra hydropyridones fused with a carbohydrate fragment. In the case of acetoacetic acid amides, mixtures of keto and enol tautomers were obtained. The stereochemistry of cyclization is discussed in detail.For Communication 1, see Ref. 1.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 409–414, February, 1996.
Keywords:levoglucosenone    /content/l4587vj175660h4w/xxlarge945.gif"   alt="  agr"   align="  BASELINE"   BORDER="  0"  >-nitrocarboxylic acid amides  acetoacetic acid amides  stereoselective heterocyclization
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