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Exciton chirality method and its application to configurational and conformational studies of natural products
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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The Exciton Contribution to the Optical Rotation of Polymers
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Chiroptical techniques and their relationship to biological molecules, big or small
inferred← citeshttps://doi.org/10.1002/recl.19790980102openalex-snapshot
X‐Ray structure of the inherently dissymmetric olefin D,L‐trans‐1,2,3,4,1′,2′,3′,4′‐octahydro‐4,4′‐biphenanthrylidene
inferred← citeshttps://doi.org/10.1007/0-306-46862-x_48openalex-snapshot
Combination of α-helix peptides with intercalator anthracene for reporting peptide-DNA interactions
inferred← citeshttps://doi.org/10.1007/978-1-4613-0315-2_17openalex-snapshot
Photoionization of Oriented Systems and Circular Dichroism
inferred← citeshttps://doi.org/10.1007/978-3-030-95990-6_12openalex-snapshot
Chiroptical Properties II: Helicity Rule or Chirality Rule
inferred← citeshttps://doi.org/10.1007/978-3-031-10457-2_1openalex-snapshot
Asian Ancistrocladus Lianas as Creative Producers of Naphthylisoquinoline Alkaloids
inferred← citeshttps://doi.org/10.1007/978-3-540-30429-6_18openalex-snapshot
Monosaccharides: Occurrence, Significance, and Properties
inferred← citeshttps://doi.org/10.1007/978-3-642-45410-3_2openalex-snapshot
Fundamental Stereochemical Concepts and Nomenclatures
inferred← citeshttps://doi.org/10.1007/978-3-642-66682-7_9openalex-snapshot
Chemical and Biological Investigations on Indian Medicinal Plants
inferred← citeshttps://doi.org/10.1007/978-3-642-74017-6_17openalex-snapshot
Stereochemical Studies on Pre-Anthraquinones and Dimeric Anthraquinone Pigments
inferred← citeshttps://doi.org/10.1007/978-3-642-74075-6_3openalex-snapshot
Fractionation and Proof of Structure of Natural Products
inferred← citeshttps://doi.org/10.1007/978-3-7091-7083-0_4openalex-snapshot
Applications of the Chiroptical Techniques to the Study of Natural Products
inferred← citeshttps://doi.org/10.1007/978-3-7091-9363-1_1openalex-snapshot
Hydrolyzable Tannins and Related Polyphenols
inferred← citeshttps://doi.org/10.1007/978-94-011-2262-7_13openalex-snapshot
Chiroptical properties of fluorescamine and MDPF condensation compounds with amino acids, amino acid esters and dipeptides
inferred← citeshttps://doi.org/10.1007/978-981-16-2458-2_10openalex-snapshot
Design, Concise Synthesis and Self-Assembly of the Mid-Sized Molecules Exploiting Bispyrrolidinoindoline Alkaloidal Scaffolds
inferred← citeshttps://doi.org/10.1007/bf00573706openalex-snapshot
Molekülstrukturanalyse durch Circulardichroismus
inferred← citeshttps://doi.org/10.1007/bf00708732openalex-snapshot
The association of inclusion complexes of cyclodextrins with azo dyes
inferred← citeshttps://doi.org/10.1007/bf02672427openalex-snapshot
“As I remember it” research on biosynthesis of fatty acids, triglycerides, squalene, and cholesterol
inferred← citeshttps://doi.org/10.1007/s00216-010-3959-2openalex-snapshot
Circular dichroism in drug discovery and development: an abridged review
inferred← citeshttps://doi.org/10.1007/s00726-023-03371-5openalex-snapshot
Applications of biaryl cyclization in the synthesis of cyclic enkephalin analogs with a highly restricted flexibility
inferred← citeshttps://doi.org/10.1007/s11418-018-1201-2openalex-snapshot
Three new 5,6,7,8-tetrahydroxy-5,6,7,8-tetrahydrochromone derivatives enantiomeric to agarotetrol from agarwood
inferred← citeshttps://doi.org/10.1007/s12272-012-0309-2openalex-snapshot
Tetrahydroanthraquinone and xanthone derivatives from the marine-derived fungus Trichoderma aureoviride PSU-F95
inferred← citeshttps://doi.org/10.1007/s13738-017-1086-0openalex-snapshot
Decades of synthesis and application of spiro cyclopropanes
inferred← citeshttps://doi.org/10.1007/s42995-026-00390-5openalex-snapshot
Discovery of antimicrobial naphtho-pyrone dimers and xanthone dimer derivatives from mangrove endophytic fungus Curvularia sp. via bioassay-guided isolation and HSQC-based DeepSAT analysis
inferred← citeshttps://doi.org/10.1016/0003-9861(87)90293-1openalex-snapshot
Stereoselective formation and hydration of benzo[c]phenanthrene 3,4-and 5,6-epoxide enantiomers by rat liver microsomal enzymes
inferred← citeshttps://doi.org/10.1016/0005-2795(78)90479-8openalex-snapshot
Effect of temperature on fluorescence and circular dichroism of Escherichia coli dihydrofolate reductase and its complexes
inferred← citeshttps://doi.org/10.1016/0006-291x(78)91172-5openalex-snapshot
Chiroptical properties of fluorescamine condensation compounds with amino acid esters in situ. Pyrrolinone chirality rule
inferred← citeshttps://doi.org/10.1016/0006-291x(78)91678-9openalex-snapshot
Circular dichroic probes for aspects of chromatin structure: Aromatic polycationic ionen probes
inferred← citeshttps://doi.org/10.1016/0006-291x(81)91204-3openalex-snapshot
Metabolism of (−)-trans-(3R,4R)-dihydroxy-3,4-dihydrochrysene to diol epoxides by liver microsomes
inferred← citeshttps://doi.org/10.1016/0008-6215(83)88042-2openalex-snapshot
Characterization of methyl glycosides at the pico- to nano-gram level
inferred← citeshttps://doi.org/10.1016/0008-6215(87)80263-xopenalex-snapshot
Relationship between circular dichroism and structure of acetyl derivatives of deoxypyranoses
inferred← citeshttps://doi.org/10.1016/0008-6215(92)80007-nopenalex-snapshot
Induced circular-dichroism spectra of complexes of cyclomalto-oligosaccharides and azo dyes containing naphthalene nuclei
inferred← citeshttps://doi.org/10.1016/0009-2614(76)80722-1openalex-snapshot
A de voe theory approach to transition metal complexes stereochemistry
inferred← citeshttps://doi.org/10.1016/0009-2797(77)90108-9openalex-snapshot
Metabolism of benzo[a]pyrene VI. Stereoselective metabolism of benzo[a]pyrene and benzo[a]pyrene 7,8-dihydrodiol to diol epoxides
inferred← citeshttps://doi.org/10.1016/0009-2797(79)90122-4openalex-snapshot
Absolute stereochemistry of the trans-dihydrodiols formed from benzo[a]anthracene by liver microsomes
inferred← citeshttps://doi.org/10.1016/0009-2797(84)90053-xopenalex-snapshot
Stereoselective metabolism of 7-methylbenz[a]anthracene: Absolute configuration of five dihydrodiol metabolites and the effect of dihydrodiol conformation on circular dichroism spectra
inferred← citeshttps://doi.org/10.1016/0009-2797(85)90022-5openalex-snapshot
Absolute configuration of trans-7,8-dihydroxy-7,8-dihydro-7-methylbenzo[a]pyrene enantiomer and the unusual quasidiequatorial conformation of the diacetate and dimenthoxyacetate derivatives
inferred← citeshttps://doi.org/10.1016/0022-2852(76)90297-6openalex-snapshot
Excited singlet states of fluoranthene
inferred← citeshttps://doi.org/10.1016/0031-9422(82)85205-9openalex-snapshot
Production of the phytotoxins radicinin and radicinol by Alternaria chrysanthemi
inferred← citeshttps://doi.org/10.1016/0031-9422(88)83047-4openalex-snapshot
(−)-Regiolone, an α-tetralone from Juglans regia: structure, stereochemistry and conformation
inferred← citeshttps://doi.org/10.1016/0031-9422(91)85065-8openalex-snapshot
An approximate estimate of self-association constants and the self-stacking conformation of Malvin quinonoidal bases studied by 1H NMR
inferred← citeshttps://doi.org/10.1016/0031-9422(92)80077-ropenalex-snapshot
Cytotoxic naphthoquinones from Mansoa alliacea
inferred← citeshttps://doi.org/10.1016/0032-3861(93)90238-6openalex-snapshot
Unique property of cyanine dyes on charged poly(l-lysine)
inferred← citeshttps://doi.org/10.1016/0040-4020(76)85163-0openalex-snapshot
Prostaglandin chemistry—V
inferred← citeshttps://doi.org/10.1016/0040-4020(76)85192-7openalex-snapshot
Prostaglandin chemistry—IV
inferred← citeshttps://doi.org/10.1016/0040-4020(77)80020-3openalex-snapshot
Influence of substitution pattern on the benzenoid transitions
inferred← citeshttps://doi.org/10.1016/0040-4020(78)87004-5openalex-snapshot
Circular dichroism of c-glycosylflavones
inferred← citeshttps://doi.org/10.1016/0040-4020(80)80222-5openalex-snapshot
Antimicrobial and antispasmodic tetrahydroanthracenes from Cassia singueana
inferred← citeshttps://doi.org/10.1016/0040-4020(94)01021-qopenalex-snapshot
Selective asymmetric dihydroxylation of polyenes
inferred← citeshttps://doi.org/10.1016/0040-4020(96)00297-9openalex-snapshot
Alkaloids from Hippeastrum equestre Herb. —5. Circular dichroism studies
inferred← citeshttps://doi.org/10.1016/0040-4020(96)00608-4openalex-snapshot
Synthetic studies on virantmycin. 2. Total synthesis of unnatural (+)-virantmycin and determination of its absolute stereochemistry
inferred← citeshttps://doi.org/10.1016/0040-4039(81)80111-6openalex-snapshot
absolute configuration of the k-region 4,5-dihydrodiols and 4,5-oxide of benzo[a]pyrene
inferred← citeshttps://doi.org/10.1016/0040-4039(95)00757-4openalex-snapshot
Arnottin II, a unique spiro compound composed of a 3, 4-dehydro-1-tetralone and a phthalide skeleton: Is it biosynthetically related to a benzo[c]phenanthridine alkaloid ?
inferred← citeshttps://doi.org/10.1016/0040-4039(96)00771-xopenalex-snapshot
The simultaneous double Diels-Alder addition of 1,1-bis(3,5-dimethylfur-2-yl)ethane; toward a new, asymmetric synthesis of long-chain polypropionate fragments and analogues
inferred← citeshttps://doi.org/10.1016/0041-0101(85)90031-5openalex-snapshot
The chemistry of brevetoxins: A review
inferred← citeshttps://doi.org/10.1016/0957-4166(94)80132-0openalex-snapshot
Synthesis and resolution of the enantiomeric trans,trans-spiro[5.5]undecane-1,7-diols and determination of their absolute configuration; (S)-(−)-spiro[5.5]undecane-1,7-dione
inferred← citeshttps://doi.org/10.1016/0957-4166(95)00043-oopenalex-snapshot
Enantioselective esterification of 5-hydroxy-2-methyl-6-(diethoxy-methyl)-1-cyclohexenecarbaldehyde. Synthesis of both enantiomers of 6-methylbicyclo[4.1.0]hept-2-ene-1,2-dicarbaldehyde
inferred← citeshttps://doi.org/10.1016/0957-4166(96)00151-6openalex-snapshot
Efficient application of lipase-catalyzed transesterification to the resolution of γ-hydroxy ketones
inferred← citeshttps://doi.org/10.1016/0957-4166(96)00331-xopenalex-snapshot
Separation of the enantiomers of anticonvulsant tricyclic pyrroloimidazolones by enantioselective HPLC. A chiral recognition model and a chiroptical study
inferred← citeshttps://doi.org/10.1016/b978-0-08-022038-3.50007-1openalex-snapshot
STRUCTURES OF TISSUE CULTURE ADDUCTS FORMED FROM POLYAROMATIC HYDROCARBONS AND NUCLEIC ACIDS
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00808-9openalex-snapshot
8.3 Perspective and Concepts: Overview of Techniques for Assigning Stereochemistry
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00846-6openalex-snapshot
8.24 Spectroscopic Analysis: Exciton Circular Dichroism for Chiral Analysis
inferred← citeshttps://doi.org/10.1016/b978-0-12-304204-0.50010-5openalex-snapshot
Determination of the Absolute Configuration of α-Amino Acids and Small Peptides by Chiroptical Means
inferred← citeshttps://doi.org/10.1016/b978-0-12-821062-8.00004-1openalex-snapshot
Chiroptical properties: Origin and applications
inferred← citeshttps://doi.org/10.1016/b978-0-32-390644-9.00014-7openalex-snapshot
Spectroscopic Analysis: Exciton Circular Dichroism for Chiral Analysis
inferred← citeshttps://doi.org/10.1016/b978-0-32-390644-9.00308-5openalex-snapshot
Perspective and Concepts: Overview of Techniques for Assigning Stereochemistry
inferred← citeshttps://doi.org/10.1016/b978-0-444-64027-7.00007-0openalex-snapshot
Chiral Molecular Tools Powerful for the Preparation of Enantiopure Compounds and Unambiguous Determination of Their Absolute Configurations by X-Ray Crystallography and/or 1H NMR Diamagnetic Anisotropy
inferred← citeshttps://doi.org/10.1016/b978-044451669-5/50013-2openalex-snapshot
Electronic circular dichroism for chiral analysis
inferred← citeshttps://doi.org/10.1016/j.bbamem.2020.183395openalex-snapshot
DAPTOMYCIN, its membrane-active mechanism vs. that of other antimicrobial peptides
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.04.007openalex-snapshot
Theoretical simulation of the electronic circular dichroism spectrum of calicheamicin
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.04.040openalex-snapshot
Termination of the structural confusion between plipastatin A1 and fengycin IX
inferred← citeshttps://doi.org/10.1016/j.bpj.2017.05.025openalex-snapshot
Molecular State of the Membrane-Active Antibiotic Daptomycin
inferred← citeshttps://doi.org/10.1016/j.chroma.2012.09.046openalex-snapshot
Advantages of electronic circular dichroism detection for the stereochemical analysis and characterization of drugs and natural products by liquid chromatography
inferred← citeshttps://doi.org/10.1016/j.cplett.2005.10.152openalex-snapshot
Detection of spectral inhomogeneities of mesoscopic thiacyanine J aggregates in solution by the apparent CD spectral measurement
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104174openalex-snapshot
Novel phthalide dimers from the aerial parts of Ligusticum sinense Oliv cv. Chaxiong
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104449openalex-snapshot
Eumitrins C-E: Structurally diverse xanthone dimers from the vietnamese lichen Usnea baileyi
inferred← citeshttps://doi.org/10.1016/j.giant.2021.100059openalex-snapshot
Self-assembled helical superstructures of polystyrene-b-poly(2-vinyl pyridine) with inversed helicity from induced chirality
inferred← citeshttps://doi.org/10.1016/j.isci.2020.100927openalex-snapshot
A Quinoline-Appended Cyclodextrin Derivative as a Highly Selective Receptor and Colorimetric Probe for Nucleotides
inferred← citeshttps://doi.org/10.1016/j.lfs.2005.12.052openalex-snapshot
The effects of oral Cardax™ (disodium disuccinate astaxanthin) on multiple independent oxidative stress markers in a mouse peritoneal inflammation model: influence on 5-lipoxygenase in vitro and in vivo
inferred← citeshttps://doi.org/10.1016/j.molliq.2024.125477openalex-snapshot
Photoisomerization-modulated supramolecular chirality inversion and energy-transfer efficiency in a cyanostilbene-glutamide-based self-assembly system
inferred← citeshttps://doi.org/10.1016/j.molstruc.2012.12.048openalex-snapshot
Chiral isothiocyanates – An approach to determination of the absolute configuration using circular dichroism measurement
inferred← citeshttps://doi.org/10.1016/j.phytochem.2005.11.026openalex-snapshot
Beccaridiol, an unusual 28-nortriterpenoid from the leaves of Diplectria beccariana
inferred← citeshttps://doi.org/10.1016/j.phytochem.2015.07.005openalex-snapshot
Diterpenoids from aerial parts of Flickingeria fimbriata and their nuclear factor-kappaB inhibitory activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.112186openalex-snapshot
Anti-inflammatory and cytotoxic carbazole alkaloids from Murraya kwangsiensis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113885openalex-snapshot
Akanthomins A–C, aphidicolin analogs from a fungus Akanthomyces sp., that inhibit cell cycle
inferred← citeshttps://doi.org/10.1016/j.phytol.2022.11.005openalex-snapshot
Kojicone C, new anti-inflammatory polyketide from insect-associated fungus Aspergillus versicolor
inferred← citeshttps://doi.org/10.1016/j.phytol.2024.05.006openalex-snapshot
Albifimbrins A and B, a pair of epimeric tetrahydrofuran-containing linear polyketide derivatives from the marine-derived fungus Albifimbria verrucaria CD1-4
inferred← citeshttps://doi.org/10.1016/j.tet.2003.09.036openalex-snapshot
Structure and biosynthetic implication of (S)-NHAB, a novel shunt product, from a disruptant of the actVI-ORFA gene for actinorhodin biosynthesis in Streptomyces coelicolor A3(2)
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