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Theoretical Calculation of Electronic Circular Dichroism of a Hexahydroxydiphenoyl-Containing Flavanone Glycoside

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Fast solvent screening via quantum chemistry: COSMO‐RS approach

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Circular dichroism, a powerful tool for the assessment of absolute configuration of flavonoids

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Circular dichroism, optical rotatory dispersion and absolute configuration of flavanones, 3-hydroxyflavanones and their glycosides

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Circular dichroism of hydrolysable tannins-I ellagitannins and gallotannins

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Conductor-like Screening Model for Real Solvents: A New Approach to the Quantitative Calculation of Solvation Phenomena

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Determination of the Absolute Configurations of Natural Products via Density Functional Theory Calculations of Vibrational Circular Dichroism, Electronic Circular Dichroism and Optical Rotation: The Schizozygane Alkaloid Schizozygine

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Determination of the Absolute Configuration of a Chiral Oxadiazol-3-one Calcium Channel Blocker, Resolved Using Chiral Chromatography, via Concerted Density Functional Theory Calculations of Its Vibrational Circular Dichroism, Electronic Circular Dichroism, and Optical Rotation

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Theoretical Calculation of Electronic Circular Dichroism of the Rotationally Restricted 3,8‘ ‘-Biflavonoid Morelloflavone

inferredcites →https://doi.org/10.1021/jp0275802openalex-snapshot

Systematic Investigation of Modern Quantum Chemical Methods to Predict Electronic Circular Dichroism Spectra

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The Current State of Ab Initio Calculations of Optical Rotation and Electronic Circular Dichroism Spectra

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Phenolic Compounds from Miconia myriantha Inhibiting Candida Aspartic Proteases

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Antitumor Agents, 129. Tannins and Related Compounds as Selective Cytotoxic Agents

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Application of electronic circular dichroism in configurational and conformational analysis of organic compounds

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COSMO: a new approach to dielectric screening in solvents with explicit expressions for the screening energy and its gradient

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The crystal structure of (S)-(–)-6-Bromo-5,7-dihydroxy-8-methyl-2-phenyl-2,3-dihydro-4H-1-benzopyran-4-one [(–)-6-bromocryptostrobin] and a 13C N.M.R. study of (±)-cryptostrobin and related substances. Revision of the structures of the natural products (±)-lawinal, u

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Tannins and Related Polyphenols of Theaceous Plants. VIII. Camelliatannins C and E, New Complex Tannins from Camellia japonica Leaves.

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Camelliatannin D, a new inhibitor of bone resorption, from Camellia japonica.

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