Conformational and Electron Density Analysis of Bicyclo[3.1.0] hexanes: All Roads Lead to Boats

Article

Authorship

de Diego Saadia, Sheila Irina ; RODRIGUEZ, JUAN BAUTISTA ; VALLEJOS, MARGARITA DE LAS MERCEDES ; SZAJNMAN, SERGIO HERNAN

Date

2024

Publishing House and Editing Place

WILEY-V C H VERLAG GMBH

Magazine

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, vol. 27 (pp. 1-10) - ISSN 1434-193X
WILEY-V C H VERLAG GMBH

ISSN

1434-193X

Summary Information provided by the agent in SIGEVA

In view of the existence of an optimal conformation for molecular recognition and bearing in mind that nucleosides exhibit a broad range of pharmaceutical properties, whereby their conformationhas a key role in molecular recognition, the tendency of the pseudosugar moiety in carbanucleosides to adopt a boat-like conformation has been studied on the basic of a bicyclo[3.1.0]hexane system, resulting in versatile drug-like scaffolds to increase molecularrecognition. It is already known that using ... In view of the existence of an optimal conformation for molecular recognition and bearing in mind that nucleosides exhibit a broad range of pharmaceutical properties, whereby their conformationhas a key role in molecular recognition, the tendency of the pseudosugar moiety in carbanucleosides to adopt a boat-like conformation has been studied on the basic of a bicyclo[3.1.0]hexane system, resulting in versatile drug-like scaffolds to increase molecularrecognition. It is already known that using this system as pseudosugar can fix the conformation in the Northern or Southern geometry, required for biological activity, according to the relative position of the three-member cycle. By mapping their energy potential surface, we investigated the preference for boat-like conformers in bicyclo[3.1.0]hexanes. DFT is utilized alongside NBO analysis to explore the enhanced stability of boat-like conformers, also considering the influence of oxygen, sulfur, and selenium heteroatoms. Additionally, charge density distribution analysis using QTAIM identifies key atoms contributing to stability changes. These findings will help to comprehend this behavior in the drug discovery process when conformationally restricted nucleosides are involved.