Theoretical exploration to the significance of n(S)/n(O) → σ* (C-COOMe) stereoelectronic interactions-Reference-Cited by-同舟云学术

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Theoretical exploration to the significance of n(S)/n(O) → σ* (C-COOMe) stereoelectronic interactions

Published:2023 Issue:1 Volume:47 Page:384-391
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Jindani Sana¹²^ORCID,Ganguly Bishwajit¹²^ORCID

Affiliation:

1. Computation and Simulation Unit (Analytical Discipline and Centralized Instrument Facility), CSIR-Central Salt and Marine Chemicals Research Institute, Bhavnagar 364002, Gujarat, India

2. Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, Uttar Pradesh, India

Abstract

Stability of the axial/equatorial conformation in α-heterosubstituted 1,3-dioxane and 1,3-dithiane systems.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/NJ/D2NJ03861G

Reference61 articles.

1. I. V.Alabugin , Stereoelectronic effects: a bridge between structure and reactivity , John Wiley & Sons , 2016

2. Anomeric effect, hyperconjugation and electrostatics: lessons from complexity in a classic stereoelectronic phenomenon

3. Theoretical Evidence for the Relevance of n(F) → σ*(C–X) (X = H, C, O, S) Stereoelectronic Interactions

4. Exploring the Origin of the Generalized Anomeric Effects in the Acyclic Nonplanar Systems

5. Density Functional Theory Computational Reexamination of the Anomeric Effect in 2-Methoxy- and 2-Cyano-1,3-dioxanes and 1,3-Dithianes. Stereoelectronic Interactions Involving the Cyano (C≡N:) Group Revealed by Natural Bond Orbital (NBO) Analysis

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