Reevaluation of Stereoelectronic Contributions to the Conformational Properties of the Phosphodiester and N3‘-Phosphoramidate Moieties of Nucleic Acids-Reference-Cited by-同舟云学术

Reevaluation of Stereoelectronic Contributions to the Conformational Properties of the Phosphodiester and N3‘-Phosphoramidate Moieties of Nucleic Acids

Published:2001-06-22 Issue:28 Volume:123 Page:6747-6755
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Banavali Nilesh K.¹,MacKerell Alexander D.¹

Affiliation:

1. Contribution from the Department of Pharmaceutical Sciences, School of Pharmacy, University of Maryland, Baltimore, 20 North Pine Street, Baltimore, Maryland 21201

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja010295w

Reference38 articles.

1. Anomeric and reverse anomeric effects in the gas phase and aqueous solution

2. Gauche effect. Stereochemical consequences of adjacent electron pairs and polar bonds

3. The application of ab initio molecular orbital theory to the anomeric effect. A comparison of theoretical predictions and experimental data on conformations and bond lengths in some pyranoses and methyl pyranosides

4. The Anomeric Effect and Related Stereoelectronic Effects at Oxygen

5. Principles of Nucleic Acid Structure

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