The interaction of the 2′-OH group with the vicinal phosphate in ribonucleoside 3′-ethylphosphate drives the sugar-phosphate backbone into unique (S,ω-) conformational state

Tetrahedron

Volumn 51, Issue 43, 1995, Pages 11775-11792

  Plavec, J ^a   Thibaudeau, C ^a   Viswanadham, G ^a   Sund, C ^a   Sandstrom A ^a   Chattopadhyaya, J ^a  

^a UPPSALA UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

RIBONUCLEOSIDE DERIVATIVE;

ARTICLE; CHEMICAL STRUCTURE; CONFORMATION; DRUG SYNTHESIS; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; STEREOCHEMISTRY; TEMPERATURE;

EID: 0028789675     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(95)00714-J     Document Type: Article

References (60)

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5. Computer-assisted pseudorotation analysis of five-membered rings by means of proton spin-spin coupling constants: ProgramPSEUROT
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8. An all atom force field for simulations of proteins and nucleic acids
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10. X-ray determination of the molecular structure of an analogue of tubercidin: deaza-1-isotubercidin
11. Interpretation of vicinal proton-proton coupling constants by a generalized Karplus relation. Conformational analysis of the exocyclic C4′-C5′ bond in nucleosides and nucleotides: Preliminary Communication