Regiochemical Aspects in Reactions of 6-Azauridinb Dialdehyde

Nucleosides and Nucleotides

Volumn 2, Issue 2, 1983, Pages 99-112

  Nemec, Josef ^a   Rhoades, Jerry M ^a  

^a UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

2 [2 HYDROXYIMINO 1 (3,5 DIOXO 1,2,4 TRIAZIN 2 YL)ETHOXY] 3 HYDROXYPROPYLIDENEHYDROXYLAMINE; DRUG ANALYSIS; DRUG IDENTIFICATION; DRUG STRUCTURE; DRUG SYNTHESIS; INFRARED SPECTROMETRY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; THEORETICAL STUDY; ULTRAVIOLET SPECTROPHOTOMETRY;

EID: 0020958950     PISSN: 07328311     EISSN: None     Source Type: Journal    
DOI: 10.1080/07328318308081252     Document Type: Article

References (19)

1. This paper is dedicated to the memory of Professor F. Sorm for his many contributions to organic chemistry and biochemistry. (b) Nemec, J,; Avery, T.L.; Rhoades, J.M. Submitted for publication. (c) This work was presented in part before the Division of Carbohydrate Chemistry at the 182nd National Meeting of the American Chemical Society, New York, N.Y., Augustl 981 (CARB 33). (d) The periodate oxidation products of carbohydrate derivatives are generally referred to as dialdehydes. Even though these compounds actually exist as equilibrium mixtures of various cyclic and acyclic forms, they react very often as typical aldehydes. The structural representation as dialdehydes and the terM dialdehyde are, therefore, a matter of convenience.
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