Theoretical Calculation of Electronic Circular Dichroism of the Rotationally Restricted 3,8‘ ‘-Biflavonoid Morelloflavone
Author:
Affiliation:
1. National Center for Natural Products Research, Research Institute of Pharmaceutical Sciences, and Department of Pharmacognosy, School of Pharmacy, The University of Mississippi, University, Mississippi 38677
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo071134z
Reference14 articles.
1. Systematic Investigation of Modern Quantum Chemical Methods to Predict Electronic Circular Dichroism Spectra
2. Determination of Absolute Configuration Using Concerted ab Initio DFT Calculations of Electronic Circular Dichroism and Optical Rotation: Bicyclo[3.3.1]nonane Diones
3. Absolute configuration, conformation, and chiral properties of flavanone-(3→8″)-flavone biflavonoids from Rheedia acuminata
4. Isolation and On-Line LC/CD Analysis of 3,8″-Linked Biflavonoids fromGnidia involucrata
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