about
Conformation inversion of bilirubin formed by reduction of the biliverdin-human serum albumin complex: evidence from circular dichroismAcid dissociation constants of bilirubin and related carboxylic acid compounds in bile salt solutions.Experimental and calculated CPL spectra and related spectroscopic data of camphor and other simple chiral bicyclic ketones.Laser action from two dipyrrinone dyes under flash-lamp pumping.Altering the Acidity and Solution Properties of Bilirubin. Methoxy and Methylthio Substituents.Amphiphilic Dipyrrinones. Methoxylated [6]-Semirubins.Circular dichroism studies at variable temperature: urobilinoid conformationA natural crystalline urobilinogen composed of d- and l-components of differing molecular weight.Homorubins and Homoverdins.Intramolecular Hydrogen Bonding and Linear Pentapyrrole Conformation.Blue light and bilirubin excretion.(m.n)-Homorubins. Syntheses and Structures.Hydrogen Bonding: HOC=O· · ·H-N vs. HOC=O· · ·H-CNICHD Conference on Kernicterus: Research on Prevention of Bilirubin-Induced Brain Injury and Kernicterus: Bench-to-Bedside--Diagnostic Methods and Prevention and Treatment Strategies.Converting 9-Methyldipyrrinones to 9-H and 9-CHO Dipyrrinones.On the existence and structure of a new urobilin of molecular weight 592.Intermolecularly Hydrogen-Bonded Dimeric Helices. Tripyrrindiones.On the structure of bilirubin in solution. 13C[1H] heteronuclear Overhauser effect NMR analyses in aqueous buffer and organic solvents.On the acid dissociation constants of bilirubin and biliverdin. pKa values from 13C NMR spectroscopy.Dissociation constants of water-insoluble carboxylic acids by 13C-NMR. pK(a)s of mesobiliverdin-XIII alpha and mesobilirubin-XIII alpha.Aqueous dissociation constants of bile pigments and sparingly soluble carboxylic acids by 13C NMR in aqueous dimethyl sulfoxide: effects of hydrogen bonding.Carboxylic Acid to Thioamide Hydrogen Bonding.1,1'-bipyrroles: synthesis and stereochemistryPhotobilirubin: an early bilirubin photoproduct detected by absorbance difference spectroscopy.On the existence of a mono-vinyl d-urobilin.On the autoxidation of bilirubin.Phototherapy and the photobiology of bilirubin.'Like a shrivelled blood orange'--bilirubin, jaundice, and phototherapy.Photochemistry of pyrroles, bile pigments and prophyrins.Oxygenation of a dipyrromethene model for bilirubin: formation of a singlet oxygen-like product.pH Dependent Chiroptical Properties of (1R,2R)- and (1S,2S)-trans-Cyclohexane Diesters and Diamides from VCD, ECD, and CPL Spectroscopy.Configurational isomerization of bilirubin and the mechanism of jaundice phototherapy.Methylvinylmaleimide from bilirubin photooxidation.The isolation of crystalline i-urobilinogen (mesobilirubinogen) from feces. Comparison with crystalline d-urobilinogen (H44) and seprartion of natural i-urobilin into optically active components.Bilirubin photooxidation products in the urine of jaundiced neonates receiving phototherapy.Thermal motion of tert-butyl groups III. tert-Butyl substituents in aromatic hydrocarbons, the view from the bottom of the well.Experimental and calculated vibrational and electronic circular dichroism spectra of 2-Br-hexahelicene.Comparative analysis of IR and vibrational circular dichroism spectra for a series of camphor-related molecules.A hydrogen-bonded 'trimer' of two symmetric dipyridones.Synthesis and metabolism of the first thia-bilirubin.
P50
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P50
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chemist
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David A. Lightner
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David A. Lightner
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David A. Lightner
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David A. Lightner
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David A. Lightner
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David A. Lightner
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David A. Lightner
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David A. Lightner
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David A Lightner
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David Lightner
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David A. Lightner
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David A. Lightner
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David A. Lightner
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David A. Lightner
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