Application of electronic circular dichroism in configurational and conformational analysis of organic compounds.
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Determination of the Absolute Configurations of Chiral Drugs Using Chiroptical SpectroscopyCircular dichroism calculation for natural productsNew Abietane and Kaurane Type Diterpenoids from the Stems of Tripterygium regeliiUnusual dimeric tetrahydroxanthone derivatives from Aspergillus lentulus and the determination of their axial chiralitiesChirality imprinting and direct asymmetric reaction screening using a stereodynamic Brønsted/Lewis acid receptorExciton circular dichroism couplet arising from nitrile-derivatized aromatic residues as a structural probe of proteins.Theoretical calculation of electronic circular dichroism of a hexahydroxydiphenoyl-containing flavanone glycoside.Designed folding of pseudopeptides: the transformation of a configurationally driven preorganization into a stereoselective multicomponent macrocyclization reaction.A new benzofuran glycoside and indole alkaloids from a sponge-associated rare actinomycete, Amycolatopsis sp.Proteasome-inhibitory and cytotoxic constituents of Garcinia lateriflora: absolute configuration of caged xanthones.4-arylflavan-3-ols as proanthocyanidin models: absolute configuration via density functional calculation of electronic circular dichroismNew hippolide derivatives with protein tyrosine phosphatase 1B inhibitory activity from the marine sponge Hippospongia lachne.Induced circular-dichroism chirality probes for selective amino acid detection through screening of a dynamic combinatorial library of lanthanide complexes.Conformational effects on the circular dichroism of Human Carbonic Anhydrase II: a multilevel computational study.Small-peptide-based organogel kit: towards the development of multicomponent self-sorting organogels.Applied circular dichroism: a facile spectroscopic tool for configurational assignment and determination of enantiopurityConformation-specific circular dichroism spectroscopy of cold, isolated chiral molecules.A simple method for the determination of enantiomeric excess and identity of chiral carboxylic acidsChiral amine enantiomeric excess determination using self-assembled octahedral Fe(II)-imine complexesSeparation of Betti Reaction Product Enantiomers: Absolute Configuration and Inhibition of Botulinum Neurotoxin ADynamic multi-component covalent assembly for the reversible binding of secondary alcohols and chirality sensingComputational-guided discovery and characterization of a sesquiterpene synthase from Streptomyces clavuligerusSynthesis and Properties of Bis-Porphyrin Molecular Tweezers: Effects of Spacer Flexibility on Binding and Supramolecular Chirogenesis.Photoinhibition and photoinhibition-like damage to the photosynthetic apparatus in tobacco leaves induced by pseudomonas syringae pv. Tabaci under light and dark conditions.Enantio- and chemoselective differentiation of protected α-amino acids and β-homoamino acids with a single copper(II) hostDistinctive effect on nerve growth factor-induced PC12 cell neurite outgrowth by two unique neolignan enantiomers from Illicium merrillianum.Bioactive Polycyclic Quinones from Marine Streptomyces sp. 182SMLY.Cytotoxic Rocaglate Derivatives from Leaves of Aglaia perviridis.Application of a High-Throughput Enantiomeric Excess Optical Assay Involving a Dynamic Covalent Assembly: Parallel Asymmetric Allylation and Ee Sensing of Homoallylic Alcohols.Eutypenoids A-C: Novel Pimarane Diterpenoids from the Arctic Fungus Eutypella sp. D-1.Anti-infective discorhabdins from a deep-water alaskan sponge of the genus Latrunculia.Attomolar DNA detection with chiral nanorod assemblies.Chiral amplification in a cyanobiphenyl nematic liquid crystal doped with helicene-like derivatives.Mechanistic and chiroptical studies on the desulfurization of epidithiodioxopiperazines reveal universal retention of configuration at the bridgehead carbon atoms.Density functional study of tetraphenylporphyrin long-range exciton couplingNucleic acid-guided assembly of aromatic chromophores.Determination of Absolute Configuration of Natural Products: Theoretical Calculation of Electronic Circular Dichroism as a ToolVCD spectroscopy as a novel probe for chirality transfer in molecular interactions.Conformational aspects in the studies of organic compounds by electronic circular dichroism.Rapid determination of enantiomeric excess: a focus on optical approaches.
P2860
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P2860
Application of electronic circular dichroism in configurational and conformational analysis of organic compounds.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Application of electronic circ ...... analysis of organic compounds.
@en
type
label
Application of electronic circ ...... analysis of organic compounds.
@en
prefLabel
Application of electronic circ ...... analysis of organic compounds.
@en
P356
P1476
Application of electronic circ ...... analysis of organic compounds.
@en
P2093
Lorenzo Di Bari
P304
P356
10.1039/B515476F
P577
2007-02-05T00:00:00Z