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Absolute Configurations of Fungal and Plant Metabolites by Chiroptical Methods. ORD, ECD, and VCD Studies on Phyllostin, Scytolide, and Oxysporone

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What this work says

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

inferredcites →https://doi.org/10.1002/9781118120187.ch26openalex-snapshot

Complexation, Solvation, and Chirality Transfer in Vibrational Circular Dichroism

inferredcites →https://doi.org/10.1002/9781118120392.ch12openalex-snapshot

Determination of Molecular Absolute Configuration: Guidelines for Selecting a Suitable Chiroptical Approach

inferredcites →https://doi.org/10.1002/chir.20475openalex-snapshot

Why is it important to simultaneously use more than one chiroptical spectroscopic method for determining the structures of chiral molecules?

inferredcites →https://doi.org/10.1002/chir.20789openalex-snapshot

Computing chiroptical properties with first‐principles theoretical methods: Background and illustrative examples

inferredcites →https://doi.org/10.1002/chir.20817openalex-snapshot

A VCD robust mode analysis of induced chirality: The case of pulegone in chloroform

inferredcites →https://doi.org/10.1002/chir.21977openalex-snapshot

On chirality transfer in electron donor–acceptor complexes. A prediction for the sulfinimine···BF3 system

inferredcites →https://doi.org/10.1002/ejoc.201100941openalex-snapshot

Regiolone and Isosclerone, Two Enantiomeric Phytotoxic Naphthalenone Pentaketides: Computational Assignment of Absolute Configuration and Its Relationship with Phytotoxic Activity

inferredcites →https://doi.org/10.1007/128_2010_72openalex-snapshot

Time-Dependent Density Functional Response Theory for Electronic Chiroptical Properties of Chiral Molecules

inferredcites →https://doi.org/10.1007/128_2010_86openalex-snapshot

Vibrational Circular Dichroism Spectroscopy of Chiral Molecules

inferredcites →https://doi.org/10.1007/s10870-009-9597-xopenalex-snapshot

X-Ray Crystal Structure of Phyllostin, a Metabolite Produced by Phyllosticta cirsii, a Potential Mycoherbicide of Cirsium arvense

inferredcites →https://doi.org/10.1016/0031-9422(79)83081-2openalex-snapshot

Oxysporone, a new metabolite from Fusarium oxysporum

inferredcites →https://doi.org/10.1016/0031-9422(91)84189-yopenalex-snapshot

Phytotoxins produced by Pestalotiopsis oenotherae, a pathogen of evening primrose

inferredcites →https://doi.org/10.1016/b978-008045382-8.00188-xopenalex-snapshot

Characterization by Circular Dichroism Spectroscopy

inferredcites →https://doi.org/10.1016/j.cplett.2004.06.011openalex-snapshot

A new hybrid exchange–correlation functional using the Coulomb-attenuating method (CAM-B3LYP)

inferredcites →https://doi.org/10.1016/j.phytochem.2012.01.011openalex-snapshot

Afritoxinones A and B, dihydrofuropyran-2-ones produced by Diplodia africana the causal agent of branch dieback on Juniperus phoenicea

inferredcites →https://doi.org/10.1016/j.tet.2007.12.010openalex-snapshot

Phyllostictines A–D, oxazatricycloalkenones produced by Phyllosticta cirsii, a potential mycoherbicide for Cirsium arvense biocontrol

inferredcites →https://doi.org/10.1016/s0040-4039(00)94366-1openalex-snapshot

The synthesis of a 10-membered benzo-oxadiyne ring

inferredcites →https://doi.org/10.1016/s0040-4039(00)98455-7openalex-snapshot

Shikimate-derived metabolites. 14.1 chiral synthesis of 5-enolpyruvyl-shikimate-3-phosphate

inferredcites →https://doi.org/10.1021/ja049185qopenalex-snapshot

Determination of the Absolute Configuration of [32](1,4)Barrelenophanedicarbonitrile Using Concerted Time-Dependent Density Functional Theory Calculations of Optical Rotation and Electronic Circular Dichroism

inferredcites →https://doi.org/10.1021/jf0731301openalex-snapshot

Phyllostoxin and Phyllostin, Bioactive Metabolites Produced by Phyllosticta cirsii, a Potential Mycoherbicide for Cirsium arvense Biocontrol

inferredcites →https://doi.org/10.1021/jo00351a015openalex-snapshot

Conversion of shikimic acid to 5-enolpyruvylshikimate 3-phosphate

inferredcites →https://doi.org/10.1021/jp020124topenalex-snapshot

Polarizable Continuum Model (PCM) Calculations of Solvent Effects on Optical Rotations of Chiral Molecules

inferredcites →https://doi.org/10.1021/jp048233qopenalex-snapshot

Harmonic Vibrational Frequencies: Scaling Factors for HF, B3LYP, and MP2 Methods in Combination with Correlation Consistent Basis Sets

inferredcites →https://doi.org/10.1021/jp073974nopenalex-snapshot

An Evaluation of Harmonic Vibrational Frequency Scale Factors

inferredcites →https://doi.org/10.1021/jp202501yopenalex-snapshot

A Single Chiroptical Spectroscopic Method May Not Be Able To Establish the Absolute Configurations of Diastereomers: Dimethylesters of Hibiscus and Garcinia Acids

inferredcites →https://doi.org/10.1021/jp710201qopenalex-snapshot

Effects of Complex Formation on Vibrational Circular Dichroism Spectra

inferredcites →https://doi.org/10.1039/b823558aopenalex-snapshot

Robust normal modes in vibrational circular dichroism spectra

inferredcites →https://doi.org/10.1039/c1cp21645gopenalex-snapshot

Reliability of computed signs and intensities for vibrational circular dichroism spectra

inferredcites →https://doi.org/10.1039/tf9302600293openalex-snapshot

The physical significance of optical rotatory power

inferredcites →https://doi.org/10.1080/00021369.1985.10866673openalex-snapshot

A New Shikimate Derivative, Methyl 5-Lactyl Shikimate Lactone, from Penicillium sp.

inferredcites →https://doi.org/10.1080/10575639308043458openalex-snapshot

Scytolide, A New Shikimate Metabolite from the FungusScytalidium Uredinicola

inferredcites →https://doi.org/10.1093/pcp/pcq055openalex-snapshot

Strigolactones as Germination Stimulants for Root Parasitic Plants

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The role of chirality in a set of key intermediates of pharmaceutical interest, 3-aryl-substituted-γ-butyrolactones, evidenced by chiral HPLC separation and by chiroptical spectroscopies

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inferred← citeshttps://doi.org/10.1080/14786419.2019.1652291openalex-snapshot

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inferred← citeshttps://doi.org/10.1080/14786419.2020.1844699openalex-snapshot

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inferred← citeshttps://doi.org/10.1177/1934578x1501001036openalex-snapshot

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inferred← citeshttps://doi.org/10.1177/1934578x1701200501openalex-snapshot

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inferred← citeshttps://doi.org/10.2174/0929867324666170310112009openalex-snapshot

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inferred← citeshttps://doi.org/10.29356/jmcs.v59i1.15openalex-snapshot

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inferred← citeshttps://doi.org/10.3114/sim.2024.108.01openalex-snapshot

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inferred← citeshttps://doi.org/10.3389/fchem.2021.734822openalex-snapshot

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inferred← citeshttps://doi.org/10.3389/fmicb.2021.688202openalex-snapshot

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inferred← citeshttps://doi.org/10.3389/fntpr.2022.1086897openalex-snapshot

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inferred← citeshttps://doi.org/10.3390/life16060873openalex-snapshot

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inferred← citeshttps://doi.org/10.3390/md15030069openalex-snapshot

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inferred← citeshttps://doi.org/10.3390/md15110339openalex-snapshot

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inferred← citeshttps://doi.org/10.3390/md16070226openalex-snapshot

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inferred← citeshttps://doi.org/10.3390/md19120714openalex-snapshot

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inferred← citeshttps://doi.org/10.3390/molecules21081056openalex-snapshot

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inferred← citeshttps://doi.org/10.3390/molecules24173022openalex-snapshot

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inferred← citeshttps://doi.org/10.3390/molecules24213913openalex-snapshot

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inferred← citeshttps://doi.org/10.3390/ph12010021openalex-snapshot

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inferred← citeshttps://doi.org/10.4172/1948-593x.1000e130openalex-snapshot

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