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Articles 1 - 3 of 3
Full-Text Articles in Social and Behavioral Sciences
Electrospray Ionisation Mass Spectrometry Of Ruthenium And Palladium Complexes With Oligonucleotides, Jennifer L. Beck, Amy Humphries, Margaret Sheil, Stephen F. Ralph
Electrospray Ionisation Mass Spectrometry Of Ruthenium And Palladium Complexes With Oligonucleotides, Jennifer L. Beck, Amy Humphries, Margaret Sheil, Stephen F. Ralph
Faculty of Science - Papers (Archive)
No abstract provided.
[60]Fullerene Amino Acids And Related Derivatives, Glenn A. Burley, Paul A. Keller, Stephen G. Pyne
[60]Fullerene Amino Acids And Related Derivatives, Glenn A. Burley, Paul A. Keller, Stephen G. Pyne
Faculty of Science - Papers (Archive)
This paper is a review of the literature concerning the preparation of [60]fullerene amino acid and peptide derivatives. The structure and applications of these derivatives to the biological and material sciences is also presented.
Synthesis Of Thiazole Analogues Of The Immunosuppressive Agent (1r,2s,3r)-2-Acetyl-4(5)-(1,2,3,4-Tetrahydroxybutyl)Imidazole, George R. Jeoffreys, Alison T. Ung, Stephen G. Pyne, Brian W. Skelton, Allan H. White
Synthesis Of Thiazole Analogues Of The Immunosuppressive Agent (1r,2s,3r)-2-Acetyl-4(5)-(1,2,3,4-Tetrahydroxybutyl)Imidazole, George R. Jeoffreys, Alison T. Ung, Stephen G. Pyne, Brian W. Skelton, Allan H. White
Faculty of Science - Papers (Archive)
The synthesis of four of the diastereoisomers of 2-acetyl-5-(1,2,3,4-tetrahydroxybutyl)thiazole and two of the diastereoisomers of 2-acetyl-5-(1,2,3,4,5-pentahydroxypentyl)thiazole and 2-acetyl-4-(1,2,3,4,5-pentahydroxypentyl)thiazole are reported. These syntheses involve the condensation of 5- or 4-metallated 2-(1,1-dimethoxyethyl)thiazoles with 2,3-O-isopropylidene-D-erythrono-1,4-lactone or 5-O-(tert-butyldimethylsilyl)-2,3-O-isopropylidene-D-ribonolactone followed by reductive ring-opening of the resulting lactols. The stereochemistries and structures of some key compounds have been determined by single crystal X-ray structural analysis.