Nome |
# |
Good Computational Practice in the Assignment of Absolute Configurations by TDDFT Calculations of ECD Spectra, file e0d6c930-bcaa-fcf8-e053-d805fe0aa794
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497
|
Circularly Polarized Luminescence from Axially Chiral BODIPY DYEmers: An Experimental and Computational Study, file e0d6c930-b704-fcf8-e053-d805fe0aa794
|
383
|
null, file e0d6c927-af0f-fcf8-e053-d805fe0aa794
|
289
|
null, file e0d6c927-b95c-fcf8-e053-d805fe0aa794
|
271
|
Cisplatin and its dibromido analogue: a comparison of chemical and biological profiles, file e0d6c92b-8473-fcf8-e053-d805fe0aa794
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259
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Synthesis and structure analysis of ferrocene-containing pseudopeptides, file e0d6c92c-f612-fcf8-e053-d805fe0aa794
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256
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Absolute configuration determination by quantum mechanical calculation of chiroptical spectra: Basics and applications to fungal metabolites, file e0d6c92b-f203-fcf8-e053-d805fe0aa794
|
251
|
Strong circularly polarized luminescence of an octahedral chromium(iii) complex, file e0d6c92d-e108-fcf8-e053-d805fe0aa794
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251
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null, file e0d6c927-ae29-fcf8-e053-d805fe0aa794
|
230
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Anti-inflammatory and α-Glucosidase Inhibitory Activities of Labdane and Norlabdane Diterpenoids from the Rhizomes of Amomum villosum, file e0d6c930-a512-fcf8-e053-d805fe0aa794
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224
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The Role of Heme Chirality in the Circular Dichroism of Heme Proteins, file e0d6c926-7c44-fcf8-e053-d805fe0aa794
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221
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Synthesis, X-ray, and Spectroscopic Study of Dissymmetric Tetrahedral Zinc(II) Complexes from Chiral Schiff Base Naphthaldiminate Ligands with Apparent Exception to the ECD Exciton Chirality, file e0d6c930-b238-fcf8-e053-d805fe0aa794
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209
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5-epi-Incensole: synthesis, X-ray crystal structure and absolute configuration by means of ECD and VCD studies in solution and solid state, file e0d6c927-c537-fcf8-e053-d805fe0aa794
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206
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Inherently chiral calix[4]arenes with planar chirality: two new entries to the family, file e0d6c926-7cca-fcf8-e053-d805fe0aa794
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188
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Chiroptical response inversion upon sample flipping in thin films of a chiral benzo[1,2-b:4,5-b′]dithiophene-based oligothiophene, file e0d6c92c-0c3c-fcf8-e053-d805fe0aa794
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157
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Asymmetric organocatalytic α-amination of 2-oxindoles with bis(2,2,2-trichloroethyl)azo-dicarboxylate, file e0d6c92d-8005-fcf8-e053-d805fe0aa794
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123
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Pyriculins A and B, two monosubstituted hex-4-ene-2,3-diols and other phytotoxic metabolites produced by Pyricularia grisea isolated from buffelgrass (Cenchrus ciliaris), file e0d6c930-c7b5-fcf8-e053-d805fe0aa794
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116
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Co(II)-induced giant vibrational CD provides a new design of methods for rapid and sensitive chirality recognition, file e0d6c930-70bf-fcf8-e053-d805fe0aa794
|
115
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Interaction of a Gold(I) Dicarbene Anticancer Drug with Human Telomeric DNA G-Quadruplex: Solution and Computationally Aided X-ray Diffraction Analysis, file e0d6c930-7175-fcf8-e053-d805fe0aa794
|
83
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Higginsianins A and B, Two Diterpenoid α-Pyrones Produced by Colletotrichum higginsianum, with in Vitro Cytostatic Activity, file e0d6c930-9289-fcf8-e053-d805fe0aa794
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65
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Chiroptical Properties in Thin Films of π-Conjugated Systems, file e0d6c92f-86eb-fcf8-e053-d805fe0aa794
|
63
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Interaction of a Gold(I) Dicarbene Anticancer Drug with Human Telomeric DNA G-Quadruplex: Solution and Computationally Aided X-ray Diffraction Analysis, file e0d6c930-7100-fcf8-e053-d805fe0aa794
|
60
|
Combined reversible switching of ECD and quenching of CPL with chiral fluorescent macrocycles, file e0d6c92b-1b26-fcf8-e053-d805fe0aa794
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58
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Efficient 1400-1600 nm Circularly Polarized Luminescence from a Tuned Chiral Erbium Complex, file 26896cb9-5592-4994-b3de-0800f5244099
|
55
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On the absolute stereochemistry of tolterodine: A circular dichroism study, file e0d6c92d-aee4-fcf8-e053-d805fe0aa794
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52
|
Remarkable near-infrared chiroptical properties of chiral Yb, Tm and Er complexes, file e0d6c931-c9c5-fcf8-e053-d805fe0aa794
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51
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ECD exciton chirality method today: a modern tool for determining absolute configurations, file e0d6c931-e591-fcf8-e053-d805fe0aa794
|
48
|
Towards the Limits of Vibrational Circular Dichroism Spectroscopy: VCD Spectra of Some Alkyl Vinylethers, file e0d6c92e-dc2c-fcf8-e053-d805fe0aa794
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44
|
null, file e0d6c931-5083-fcf8-e053-d805fe0aa794
|
25
|
Three Sesquiterpenoid Dimers from Chloranthus japonicus: Absolute Configuration of Chlorahololide A and Related Compounds, file e0d6c92e-fb75-fcf8-e053-d805fe0aa794
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24
|
Enantioselective Gel Phase Synthesis of Metal–Organic Materials, file e0d6c932-1769-fcf8-e053-d805fe0aa794
|
16
|
Interaction of gold N-heterocyclic carbenes with nucleic acids, file e0d6c931-65d3-fcf8-e053-d805fe0aa794
|
14
|
Circularly polarized light at the mirror: Caveats and opportunities, file e0d6c92f-15d0-fcf8-e053-d805fe0aa794
|
12
|
Emergent Nonreciprocal Circularly Polarized Emission from an Organic Thin Film, file e0d6c92f-4980-fcf8-e053-d805fe0aa794
|
10
|
Organocatalytic alkylation of carbohydrate-containing aldehydes with dihydroquinoline N,O-acetals: Absolute configuration of 1,2-dihydroquinolines, file e0d6c92e-0f5a-fcf8-e053-d805fe0aa794
|
8
|
Tunable Excimer Circularly Polarized Luminescence in Isohexide Derivatives from Renewable Resources, file e0d6c931-e58d-fcf8-e053-d805fe0aa794
|
8
|
Impact and amplification of chirality in the aggregation of leucine-appended poly(p-phenylene ethynylene) (PPE), file e0d6c92b-eedc-fcf8-e053-d805fe0aa794
|
7
|
Symmetry-Dependent Vibrational Circular Dichroism Enhancement in Co(II) Salicylaldiminato Complexes, file e0d6c930-8adb-fcf8-e053-d805fe0aa794
|
5
|
Emergent Nonreciprocal Circularly Polarized Emission from an Organic Thin Film, file c85d85ab-5a04-414f-8507-764cc114fc2c
|
4
|
Chirality at metal and helical ligand folding in optical isomers of chiral bis(naphthaldiminato)nickel(II) complexes, file e0d6c92e-b458-fcf8-e053-d805fe0aa794
|
4
|
Exploiting isohexide scaffolds for the preparation of chiral ionic liquids tweezers, file e0d6c92f-9217-fcf8-e053-d805fe0aa794
|
4
|
Direct enantioselective vinylogous Mannich-type reactions of acyclic enals: New experimental insights into the E/Z-dilemma, file e0d6c931-18b7-fcf8-e053-d805fe0aa794
|
4
|
Synthesis and Characterization of Bis[(RorS)-N-1-(X-C6H4)ethyl-2-oxo-1-naphthaldiminato-κ2N,O]-Λ/Δ-cobalt(II) (X = H,p-CH3O,p-Br) with Symmetry- And Distance-Dependent Vibrational Circular Dichroism Enhancement and Sign Inversion, file e0d6c931-3f4e-fcf8-e053-d805fe0aa794
|
4
|
Application of the Ugi reaction with multiple amino acid-derived components: Synthesis and conformational evaluation of piperazine-based minimalist peptidomimetics, file e0d6c926-8c1b-fcf8-e053-d805fe0aa794
|
3
|
Polyoxygenated cyathane diterpenoids from the mushroom Cyathus africanus, and their neurotrophic and anti-neuroinflammatory activities, file e0d6c92a-55eb-fcf8-e053-d805fe0aa794
|
3
|
The role of magnetic–electric coupling in exciton-coupled ECD spectra: the case of bis-phenanthrenes, file e0d6c92b-ea98-fcf8-e053-d805fe0aa794
|
3
|
Stereochemical analysis of beta-keto sulfoxides by circular dichroism, file e0d6c92c-215e-fcf8-e053-d805fe0aa794
|
3
|
Unique Aggregation of Sterigmatocystin in Water Yields Strong and Specific Circular Dichroism Response Allowing Highly Sensitive and Selective Monitoring of Bio-Relevant Interactions, file e0d6c92d-e360-fcf8-e053-d805fe0aa794
|
3
|
Emergent Nonreciprocal Circularly Polarized Emission from an Organic Thin Film, file e0d6c92f-54f5-fcf8-e053-d805fe0aa794
|
3
|
Ring D-Modified and Highly Reduced Angucyclinones From Marine Sediment-Derived Streptomyces sp, file e0d6c931-8da7-fcf8-e053-d805fe0aa794
|
3
|
Conformational aspects in the studies of organic compounds by electronic circular dichroism, file e0d6c926-29e4-fcf8-e053-d805fe0aa794
|
2
|
The degradation of Burmese lacquer (thitsi) as observed in samples from two cultural artefacts, file e0d6c929-09f6-fcf8-e053-d805fe0aa794
|
2
|
How and how much molecular conformation affects electronic circular dichroism: The case of 1,1-diarylcarbinols, file e0d6c92a-23ac-fcf8-e053-d805fe0aa794
|
2
|
From Mesocates to Helicates: Structural, Magnetic and Chiro-Optical Studies on Nickel(II) Supramolecular Assemblies Derived from Tetradentate Schiff Bases, file e0d6c92b-0aff-fcf8-e053-d805fe0aa794
|
2
|
Broad-Range Spectral Analysis for Chiral Metal Coordination Compounds: (Chiro)optical Superspectrum of Cobalt(II) Complexes, file e0d6c92b-1544-fcf8-e053-d805fe0aa794
|
2
|
Incensfuran: Isolation, X-ray crystal structure and absolute configuration by means of chiroptical studies in solution and solid state, file e0d6c92c-1405-fcf8-e053-d805fe0aa794
|
2
|
Synthesis and mode of action studies of N-[(-)-jasmonyl]-S-tyrosin and ester seiridin jasmonate, file e0d6c92c-1761-fcf8-e053-d805fe0aa794
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2
|
For a correct application of the CD exciton chirality method: The case of laucysteinamide A, file e0d6c92c-49c2-fcf8-e053-d805fe0aa794
|
2
|
Phytotoxic activity of metabolites isolated from Rutstroemia sp.n., the causal agent of bleach blonde syndrome on cheatgrass (Bromus tectorum), file e0d6c92c-560e-fcf8-e053-d805fe0aa794
|
2
|
Interaction of a Gold(I) Dicarbene Anticancer Drug with Human Telomeric DNA G-Quadruplex: Solution and Computationally Aided X-ray Diffraction Analysis, file e0d6c930-8ce9-fcf8-e053-d805fe0aa794
|
2
|
Systematic Investigation of CD Spectra of Aryl Benzyl Sulfoxides Interpreted by Means of TDDFT Calculations, file e0d6c926-2ce9-fcf8-e053-d805fe0aa794
|
1
|
Vibronic Coupling Dominates the Electronic Circular Dichroism of the Benzene Chromophore 1Lb band, file e0d6c926-39e6-fcf8-e053-d805fe0aa794
|
1
|
Natural alpha-Amino Acid-Functionalized Poly(phenyleneethynylene)s (PPEs): Synthesis and Chiroptical Characterization of Aggregate States, file e0d6c926-d7db-fcf8-e053-d805fe0aa794
|
1
|
The role of magnetic–electric coupling in exciton-coupled ECD spectra: the case of bis-phenanthrenes, file e0d6c927-b965-fcf8-e053-d805fe0aa794
|
1
|
null, file e0d6c92b-edbe-fcf8-e053-d805fe0aa794
|
1
|
null, file e0d6c92b-ef0f-fcf8-e053-d805fe0aa794
|
1
|
null, file e0d6c92b-ef13-fcf8-e053-d805fe0aa794
|
1
|
Higginsianins A and B, Two Diterpenoid α-Pyrones Produced by Colletotrichum higginsianum, with in Vitro Cytostatic Activity, file e0d6c930-7417-fcf8-e053-d805fe0aa794
|
1
|
Synthesis, X-ray, and Spectroscopic Study of Dissymmetric Tetrahedral Zinc(II) Complexes from Chiral Schiff Base Naphthaldiminate Ligands with Apparent Exception to the ECD Exciton Chirality, file e0d6c930-cb4d-fcf8-e053-d805fe0aa794
|
1
|
Good Computational Practice in the Assignment of Absolute Configurations by TDDFT Calculations of ECD Spectra, file e0d6c930-cc42-fcf8-e053-d805fe0aa794
|
1
|
Elusive π-helical peptide foldamers spotted by chiroptical studies, file e0d6c932-0282-fcf8-e053-d805fe0aa794
|
1
|
Totale |
5.026 |