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Social and Behavioral Sciences Commons

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Physical Sciences and Mathematics

University of Wollongong

Faculty of Science - Papers (Archive)

1999

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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 Jan 1999

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.


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 Jan 1999

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.


[60]Fullerene Amino Acids And Related Derivatives, Glenn A. Burley, Paul A. Keller, Stephen G. Pyne Jan 1999

[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.