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Journal of the American Chemical Society

Volumn 123, Issue 20, 2001, Pages 4781-4791

2-Deoxy-β-D-erythro-pentofuranose: Hydroxymethyl group conformation and substituent effects on molecular structure, ring geometry, and NMR spin-Spin coupling constants from quantum chemical calculations

(3) Cloran, F a Carmichael, I b Serianni, A S a

a UNIVERSITY OF NOTRE DAME (United States)

b UNIVERSITY OF NOTRE DAME (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BOND TORSIONS;

CHEMICAL BONDS; DISCRETE FOURIER TRANSFORMS; DNA; MOLECULAR ORIENTATION; NUCLEAR MAGNETIC RESONANCE; RNA;

CONFORMATIONS;

2 DEOXY BETA DEXTRO ERYTHRO PENTOFURANOSE; FURAN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CALCULATION; CHEMICAL ANALYSIS; CHEMICAL BOND; CHEMICAL STRUCTURE; CORRELATION FUNCTION; ENERGY; GEOMETRY; NUCLEAR MAGNETIC RESONANCE; PREDICTION; QUANTUM CHEMISTRY; THEORY;

CHEMISTRY, PHYSICAL; GLYCOSIDES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; QUANTUM THEORY; RIBOSEMONOPHOSPHATES;

EID: 0034827973 PISSN: 00027863 EISSN: None Source Type: Journal
DOI: 10.1021/ja002525x Document Type: Article

Times cited : (54)

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