B
Brian W. Skelton
Researcher at University of Western Australia
Publications - 1662
Citations - 33374
Brian W. Skelton is an academic researcher from University of Western Australia. The author has contributed to research in topics: Crystal structure & Ligand. The author has an hindex of 69, co-authored 1646 publications receiving 31889 citations. Previous affiliations of Brian W. Skelton include Monash University, Clayton campus & State University of Malang.
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Chelidamic acid monohydrate: the proton complex of a multidentate ligand
TL;DR: Chelidamic acid, 4-hydroxypyridine-2,6-dicarboxylic acid, is found to be zwitterionic in its solid monohydrate form, C7H5NO5·H2O, with the aryloxide and one car boxylate group remaining protonated, but the other carboxyl-ate group losing its proton to the pyridine N atom.
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Syntheses and Structural Studies of Several Group 8 Metal Complexes Derived from 1,3-Butadiyne
Michael I. Bruce,Marcus L. Cole,Marcus L. Cole,Karine Costuas,Benjamin G. Ellis,Kathy A. Kramarczuk,Claude Lapinte,Brian K. Nicholson,Gary J. Perkins,Brian W. Skelton,Allan H. White,Natasha N. Zaitseva +11 more
TL;DR: In this paper, the preparation, characterization, and single-crystal X-ray diffraction molecular structure determinations of four complexes containing metal-ligand centers linked by chains of C(sp) atoms are described.
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Molecular structure of terrecyclodiol : A derivative of the antifungal metabolite terrecyclic acid A from Aspergillus terreus
TL;DR: A strain of Aspergillus terreus, which was isolated from organic mulch and inhibited the growth of the plant pathogen Phytophthora cinnamomi, produces an antifungal metabolite when grown in liquid culture that is identified as terrecyclic acid A.
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Cluster chemistry: LXXXVIII. Reactions between Ru5(μ5-C2PPh2)(μ-PPh2)(CO)13 and thiols. Formation and X-ray structures of Ru5 clusters containing C2H, C2PPh2 and CCH(PPh2) ligands
TL;DR: In this paper, the major products of the reaction with thiophenol were identified: Ru 5 (μ-H)(μ 5 -C 2 PPh 2 )(μ 3 -SR)(μ-PPh2 )(CO) 12 [R Me (2 ; 58%), Ph ( 3 ; 64%)].
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Chiral sulfur compounds. Part 25. Diastereoselective 1,2-additions of lithiated (+)-(S)-N-tert-butyldiphenylsilyl-S-methyl-S-phenylsulfoximine to ketones
TL;DR: In this paper, the relative stereochemistries of four β-hydroxy sulfoximine adducts have been unequivocally determined from single-crystal X-ray structural analysis.